Clinical Trials for Bone Infections

Currently registered clinical trials for Bone Infections from ClinicalTrials.gov. 26 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Bone Infections from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 26
  • Active, not recruiting: 6
  • Completed: 11
  • Other: 7

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00001316 — Viral Load in Blood and Lymph Tissues in People Living With HIV

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment400
Study TypeOBSERVATIONAL
ConditionsHIV

This is a study to determine the effect of the human immunodeficiency virus (HIV) on lymphoid tissues (e.g., lymph nodes) as compared to peripheral white blood cells. We have shown in previous studies that the lymph node is a major site of accumulation of HIV in the body, as well as being a site where much of the viral replication occurs which leads to the destruction of the body’s immune syste…

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1029
Study TypeOBSERVATIONAL
ConditionsHIV; Kaposi’s Sarcoma; Lymphomas; Multicentric Castleman’s Disease; Primary Effusion Lymphoma

BACKGROUND:

  • A number of important scientific advances can be made through the study of blood, bone marrow, tumor, or other tissue samples from patients with HIV infection, infection with Kaposi s sarcoma associated herpesvirus (KSHV), infection with other oncogenic viruses, or cancer.
  • This protocol provides a mechanism to affect a variety of such studies.

OBJECTIVES:

-Acquisition of seru…

NCT01137825 — Registry of Older Patients With Cancer

StatusRecruiting
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment3000
Study TypeOBSERVATIONAL
ConditionsChronic Myeloproliferative Disorders; Cognitive/Functional Effects; Leukemia; Lymphoma; Lymphoproliferative Disorder

RATIONALE: Gathering information about older patients with cancer may help the study of cancer in the future.

PURPOSE: This research study is gathering information from older patients with cancer into a registry.

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment600
Study TypeOBSERVATIONAL
ConditionsGATA2 Deficiency

Background:

- GATA2 deficiency is a genetic disorder that can cause problems with a person s immune system and other body systems. Some people who have this disorder develop few problems from it. Others can have a wide range of health problems, from skin problems, to hearing loss, to cancer. These problems can happen at any age. Researchers want to study GATA2 deficiency to better understand …

NCT03394365 — A Phase 3 Study of Tabelecleucel for Participants With Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative Disease After Failure With Rituximab or Rituximab and Chemotherapy

StatusRecruiting
PhasePhase 3
SponsorPierre Fabre Medicament
Enrollment115
Study TypeINTERVENTIONAL
ConditionsEpstein-Barr Virus+ Associated Post-transplant Lymphoproliferative Disease (EBV+ PTLD); Solid Organ Transplant Complications; Lymphoproliferative Disorders; Allogeneic Hematopoietic Cell Transplant; Stem Cell Transplant Complications
Interventions

The purpose of this study is to determine the clinical benefit and characterize the safety profile of tabelecleucel for the treatment of Epstein-Barr virus-associated post-transplant lymphoproliferative disease (EBV+ PTLD) in the setting of (1) solid organ transplant (SOT) after failure of rituximab (SOT-R) and rituximab plus chemotherapy (SOT-R+C) or (2) allogeneic hematopoietic cell transplan…

StatusRecruiting
PhasePhase 2
SponsorMasonic Cancer Center, University of Minnesota
Enrollment300
Study TypeINTERVENTIONAL
ConditionsAcute Leukemia; Acute Myeloid Leukemia; Acute Lymphoblastic Leukemia; Lymphoma; Chronic Myelogenous Leukemia
Interventions;

This is a Phase II study of allogeneic hematopoietic stem cell transplant (HCT) using a myeloablative preparative regimen (of either total body irradiation (TBI); or, fludarabine/busulfan for patients unable to receive further radiation). followed by a post-transplant graft-versus-host disease (GVHD) prophylaxis regimen of post-transplant cyclophosphamide (PTCy), tacrolimus (Tac), and mycopheno…

NCT03810196 — CD45RA Depleted Peripheral Stem Cell Addback for Viral or Fungal Infections Post TCRαβ/CD19 Depleted HSCT

StatusRecruiting
PhaseN/A
SponsorChildren’s Hospital of Philadelphia
Enrollment50
Study TypeINTERVENTIONAL
ConditionsAcute Leukemia; Acute Myeloid Leukemia; Myelodysplastic Syndromes; Acute Lymphoblastic Leukemia; Mixed Lineage Leukemia
Interventions

The major morbidities of allogeneic hematopoietic stem cell transplant with non-human leukocyte antigen (HLA) matched siblings are graft vs host disease (GVHD) and life threatening infections. T depletion of the donor hematopoietic stem cell graft is effective in preventing GVHD, but immune reconstitution is slow, increasing the risk of infections. An addback of donor CD45RA (naive T cells) dep…

NCT03779854 — Naive T Cell Depletion for Preventing Chronic Graft-versus-Host Disease in Children and Young Adults With Blood Cancers Undergoing Donor Stem Cell Transplant

StatusRecruiting
PhasePhase 2
SponsorFred Hutchinson Cancer Center
Enrollment68
Study TypeINTERVENTIONAL
ConditionsAcute Biphenotypic Leukemia; Acute Leukemia; Acute Leukemia of Ambiguous Lineage; Acute Lymphoblastic Leukemia; Acute Undifferentiated Leukemia
Interventions; ;

This phase II trial studies how well naive T-cell depletion works in preventing chronic graft-versus-host disease in children and young adults with blood cancers undergoing donor stem cell transplant. Sometimes the transplanted white blood cells from a donor attack the body’s normal tissues (called graft versus host disease). Removing a particular type of T cell (naive T cells) from the donor c…

NCT04195633 — Donor Stem Cell Transplant With Treosulfan, Fludarabine, and Total-Body Irradiation for the Treatment of Hematological Malignancies

StatusRecruiting
PhasePhase 2
SponsorFred Hutchinson Cancer Center
Enrollment60
Study TypeINTERVENTIONAL
ConditionsAcute Leukemia; Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Adult Diffuse Large Cell Lymphoma; Anaplastic Large Cell Lymphoma
Interventions; ;

This phase II trial studies how well a donor stem cell transplant, treosulfan, fludarabine, and total-body irradiation work in treating patients with blood cancers (hematological malignancies). Giving chemotherapy and total-body irradiation before a donor stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. I…

NCT04751396 — Testing of an Educational Tool for Patients With Melanoma and Pre-Existing Autoimmune Disease Who Are Candidates for Immune Checkpoint Inhibitors

StatusRecruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Enrollment125
Study TypeOBSERVATIONAL
ConditionsAnkylosing Spondylitis; Autoimmune Disease; Crohn Disease; Enteropathic Arthritis; Enteropathic Spondylitis
Interventions; ;

This study learn how easily patients can use an educational tool that will be created for patients with melanoma and pre-existing autoimmune diseases who receive or will receive immune checkpoint inhibitor drugs. Patients will be asked their opinions about the design, accessibility, and content of the tool. Researchers will use the information collected to improve the educational materials that…

NCT05470491 — Trial of Allogeneic Reduced-Intensity, HLA-Haploidentical Allogeneic Hematopoietic Cell Bone Marrow Transplantation Followed by Graft-versus-Host-Disease (GVHD) Prophylaxis With Cyclophosphamide, Bortezomib and Maraviroc for Hematologic Malignancies …

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment265
Study TypeINTERVENTIONAL
ConditionsHIV; Hematologic Malignancies
Interventions; ;

Background:

People living with HIV(PLWH) are at a higher risk for cancers that may be curable with a bone marrow transplant. HIV infection itself is no longer a reason to not get a transplant, for patients who otherwise have a standard reason to need transplant.

Objective:

This study is being done to see if a new combination of drugs (cyclophosphamide, maraviroc, and bortezomib) is both safe…

NCT05805605 — Allo HSCT Using RIC and PTCy for Hematological Diseases

StatusRecruiting
PhasePhase 2
SponsorMasonic Cancer Center, University of Minnesota
Enrollment56
Study TypeINTERVENTIONAL
ConditionsAcute Myelogenous Leukemia; Acute Lymphocytic Leukemia; Biphenotypic Acute Leukemia; Undifferentiated Leukemia; Prolymphocytic Leukemia
Interventions; ;

This is a Phase II study following subjects proceeding with our Institutional non-myeloablative cyclophosphamide/ fludarabine/total body irradiation (TBI) preparative regimen followed by a related, unrelated, or partially matched family donor stem cell infusion using post-transplant cyclophosphamide (PTCy), sirolimus and MMF GVHD prophylaxis.

NCT05794880 — MCW Alpha/Beta T-Cell and B-Cell Depletion With Targeted ATG Dosing

StatusRecruiting
PhaseN/A
SponsorMedical College of Wisconsin
Enrollment40
Study TypeINTERVENTIONAL
ConditionsLeukemia; Acute Myeloid Leukemia in Remission; Myelodysplasia; Acute Lymphoblastic Leukemia in Remission; Chronic Myelogenous Leukemia - Chronic Phase
Interventions

This is a single arm pilot study for patients with hematologic malignancies receiving unrelated or haploidentical related mobilized peripheral stem cells (PSCs) using the CliniMACS system for alpha/beta T cell depletion plus CD19+ B cell depletion with individualized ALC-based dosing of ATG to study impact on engraftment, GVHD, and disease free survival

NCT05421741 — Prophylactic Antibiotic Coated Nail to Prevent Infection: A Clinical Trial

StatusRecruiting
PhasePhase 4
SponsorWake Forest University Health Sciences
Enrollment484
Study TypeINTERVENTIONAL
ConditionsOsteomyelitis Tibia; Tibial Fractures; Open Tibia Fracture
Interventions;

This prospective randomized clinical trial will compare outcomes between patients treated primarily with a prophylactic antibiotic coated nail and those treated with traditional standard of care intramedullary (IM) nailing.

NCT05699174 — PO vs IV Antibiotics for the Treatment of Infected Nonunion of Fractures After Fixation

StatusRecruiting
PhasePhase 3
SponsorMajor Extremity Trauma Research Consortium
Enrollment250
Study TypeINTERVENTIONAL
ConditionsInfections; Infected Wound; Nonunion of Fracture; Injury Leg; Amputation
Interventions;

This is a Phase III clinical randomized control trial to investigate differences between patient with an infected nonunion treated by PO vs. IV antibiotics. The study population will be 250 patients, 18 years or older, being treated for infected nonunion after internal fixation of a fracture with a segmental defect less than one centimeter. Patients will be randomly assigned to either the treat…

NCT06131801 — Pharmacokinetic Study of Venetoclax Tablets Crushed and Dissolved Into a Solution

StatusRecruiting
PhaseN/A
SponsorChildren’s Hospital Medical Center, Cincinnati
Enrollment30
Study TypeOBSERVATIONAL
ConditionsHematologic Malignancy; Leukemia; Lymphoma; Acute Lymphocytic Leukemia; ALL
Interventions

The use of venetoclax-based therapies for pediatric patients with relapsed or refractory malignancies is increasingly common outside of the clinical trial setting. For patients who cannot swallow tablets, it is common to crush the tablets and dissolve them in liquid to create a solution. However, no PK data exists in adults or children using crushed tablets dissolved in liquid in this manner, a…

NCT07653295 — Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Revision Hip Prosthesis System

StatusRecruiting
PhaseN/A
SponsorTIPMED Medical Device Manufacturing Ltd. Co.
Enrollment35
Study TypeOBSERVATIONAL
ConditionsRevision Hip Arthroplasty; Aseptic Loosening of Prosthetic Joint; Prostheses-related Infections; Joint Instability; Periprosthetic Fractures
Interventions

This is a multicenter, prospective, observational, post-market clinical follow-up (PMCF) study designed to evaluate the safety and clinical performance of the Tipmed™ Revision Hip Prosthesis System in adult participants undergoing revision hip arthroplasty. The study aims to gather real-world clinical evidence on the 24-month post-operative safety profile, potential complications, and functiona…

NCT05766670 — Intramedullary Calcium Sulfate Antibiotic Depot

StatusRecruiting
PhasePhase 3
SponsorWake Forest University Health Sciences
Enrollment497
Study TypeINTERVENTIONAL
ConditionsOpen tíbia Fracture; Osteomyelitis Tibia; Tibial Fractures
Interventions; ;

The goal of this randomized clinical trial is to study the best treatment for open lower leg fractures to prevent infection. The main questions it aims to answer is if treating tibia fracture patients with a calcium sulfate antibiotic depot is better at preventing infection that the standard of care.

NCT06056297 — A Study of Mavorixafor in Participants With Congenital and Acquired Primary Autoimmune and Idiopathic Chronic Neutropenic Disorders Who Are Experiencing Recurrent and/or Serious Infections

StatusRecruiting
PhasePhase 3
SponsorX4 Pharmaceuticals
Enrollment176
Study TypeINTERVENTIONAL
ConditionsNeutropenia
Interventions;

The purpose of this study is to demonstrate the efficacy and evaluate the safety and tolerability of mavorixafor in participants with congenital or acquired primary autoimmune and idiopathic chronic neutropenic disorders who are experiencing recurrent and/or serious infections as assessed by demonstrating its clinical benefit and increasing levels of circulating neutrophils.

NCT06395103 — Substudy 01A: Zilovertamab Vedotin in Pediatric and Young Adult Participants With Hematologic Malignancies or Solid Tumors (MK-9999-01A/LIGHTBEAM-U01)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorMerck Sharp & Dohme LLC
Enrollment90
Study TypeINTERVENTIONAL
ConditionsB-cell Acute Lymphoblastic Leukemia; Diffuse Large B-cell Lymphoma; Burkitt Lymphoma; Neuroblastoma; Ewing Sarcoma
Interventions

Substudy 01A is part of a platform study. The purpose of this study is to assess the efficacy and safety of zilovertamab vedotin in pediatric participants with relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL), diffuse large B-cell lymphoma (DLBCL)/Burkitt lymphoma, or neuroblastoma and in pediatric and young adult participants with Ewing sarcoma.

NCT07661784 — Salivary Biomarkers in Periodontal Disease Progression

StatusRecruiting
PhaseN/A
SponsorSuleyman Demirel University
Enrollment240
Study TypeOBSERVATIONAL
ConditionsPeriodontal Disease; Gingivitis and Periodontal Diseases; Periodontitis
Interventions

This study aims to evaluate salivary biomarkers associated with bone remodeling during the transition from periodontal health to disease. Periodontal diseases are characterized by chronic inflammation that can lead to connective tissue destruction and alveolar bone loss. Although diagnosis is primarily based on clinical and radiographic findings, these methods may not fully reflect disease acti…

NCT07285044 — The Cancer Connected Access and Remote Expertise Beyond Walls Program to Provide In-Home Cancer Treatment and Improve Treatment Satisfaction in Cancer Patients Living in the Florida Panhandle and Surrounding Areas

StatusRecruiting
PhasePhase 2
SponsorMayo Clinic
Enrollment27
Study TypeINTERVENTIONAL
ConditionsAmyloidosis; Basal Cell Carcinoma; Biliary Tract Carcinoma; Bladder Carcinoma; Breast Carcinoma
Interventions; ;

This phase II trial studies whether providing cancer treatment in the home is preferred over the traditional clinic setting and if it improves treatment satisfaction in cancer patients living in the Florida Panhandle and surrounding areas. Typically, drug-related cancer care is provided at a medical center which causes patients to have to spend considerable time away from their family, friends,…

NCT07654647 — Clinical Evaluation of Patient-Specific 3D-Printed Titanium Implants for Facial Reconstruction.

StatusRecruiting
PhaseN/A
SponsorTishreen University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsHemifacial Microsomia; Mucormycosis; Oral Squamous Cell Carcinoma; Microgenia; Facial Asymmetry
Interventions

This clinical study aims to evaluate the effectiveness of patient-specific 3D-printed titanium facial implants in the reconstruction and aesthetic correction of facial defects. The study will include patients presenting with congenital, traumatic, or post-surgical facial deformities requiring reconstructive intervention.

Eligible participants will undergo preoperative clinical assessment and r…

NCT07615491 — PMCF Study on the Effectiveness and Safety of METROSAN Spinal Systems and BONEGRAFT Filling Materials

StatusRecruiting
PhaseN/A
SponsorMetrosan End. ve Elk. Mek. Cihazlar ve Tibbi Malz. San. Tic. Ltd. Co.
Enrollment561
Study TypeOBSERVATIONAL
ConditionsDegenerative Disc Disease (DDD); Spinal Stenosis; Spondylolisthesis; Spinal Deformities; Spinal Tumors
Interventions; ;

This is a prospective, multi-center, observational Post-Market Clinical Follow-Up (PMCF) study designed to collect additional safety and clinical performance data on CE-marked Titania® spinal instrumentation and fusion systems, and Bonegraft® bone filling materials (synthetic bone grafts and bone cements). The study aims to evaluate short-term (12-month) safety and effectiveness, identify previ…

NCT07270380 — Antibiotic Device for Osteomyelitis of the Extremities Pivotal Trial - Genex With Gentamicin.

StatusRecruiting
PhaseN/A
SponsorBiocomposites Ltd
Enrollment139
Study TypeINTERVENTIONAL
ConditionsOsteomyelitis
Interventions

The purpose of this trial is to determine if genex with gentamicin (genex G) an antibiotic loaded bone void filler, works to treat and is a safe option as part of the surgical treatment of osteomyelitis in the extremities.

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsTrisomy 8 Mosaicism; Trisomy 8 Associated Autoinflammatory Disease; Mucosal Ulcerations

Study Description:

This is a natural history protocol designed to characterize the clinical spectrum of trisomy 8 mosaicism and trisomy 8-associated autoinflammatory disease (TRIAD) and related autoinflammatory disorders and further evaluate approaches to screening, diagnosis, and management. We will enroll affected patients and their unaffected relatives and collect a variety of clinical data…

Active, Not Recruiting

NCT00544115 — Donor Peripheral Stem Cell Transplant in Treating Patients With Advanced Hematologic Cancer or Other Disorders

StatusActive, not recruiting
PhasePhase 2
SponsorCity of Hope Medical Center
Enrollment260
Study TypeINTERVENTIONAL
ConditionsChronic Myeloproliferative Disorders; Graft Versus Host Disease; Leukemia; Lymphoma; Multiple Myeloma and Plasma Cell Neoplasm
Interventions; ;

RATIONALE: Giving chemotherapy and total-body irradiation before a donor peripheral stem cell transplant helps stop the growth of cancer or abnormal cells. It also helps stop the patient’s immune system from rejecting the donor’s stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient’s bone marrow make stem cells, red blood cells, white blood…

NCT00710892 — CASPALLO: Allodepleted T Cells Transduced With Inducible Caspase 9 Suicide Gene

StatusActive, not recruiting
PhasePhase 1
SponsorBaylor College of Medicine
Enrollment10
Study TypeINTERVENTIONAL
ConditionsAcute Lymphoblastic Leukemia; Non-Hodgkin’s Lymphoma; Myelodysplastic Syndrome; Chronic Myeloid Leukemia
Interventions

Patients are being asked to participate in this study because they will be receiving a stem cell transplant as treatment for their disease. As part of the stem cell transplant, they will be given very strong doses of chemotherapy, which will kill off all their existing stem cells. Stem cells are created in the bone marrow. They grow into different types of blood cells that we need, including re…

NCT01494103 — Administration of Donor T Cells With the Caspase-9 Suicide Gene

StatusActive, not recruiting
PhasePhase 1
SponsorBaylor College of Medicine
Enrollment15
Study TypeINTERVENTIONAL
ConditionsAcute Lymphoblastic Leukemia; Myelodysplastic Syndrome; Acute Myeloid Leukemia; Chronic Myelogenous Leukemia; Non Hodgkin Lymphoma
Interventions;

Patients will be receiving a stem cell transplant as treatment for their disease. As part of the stem cell transplant, patients will be given very strong doses of chemotherapy, which will kill all their existing stem cells.

A close relative of the patient will be identified, whose stem cells are not a perfect match for the patient’s, but can be used. This type of transplant is called “allogene…

NCT04742387 — Assessment of Bone Mineral Density in People Living With HIV and KSHV Associated Malignancies: A Retrospective Longitudinal Analysis

StatusActive, not recruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment40
Study TypeOBSERVATIONAL
ConditionsKaposi Sarcoma; KSHV Associated Multicentric Castleman Disease; Primary Effusion Lymphoma; IL-6 Related KSHV Associated Cytokine Syndrome

Background:

Some people with human immunodeficiency virus (HIV) are on antiretroviral therapy (ART). Their cells have shown to age faster than expected. This puts them at higher risk for a range of age-related diseases about 10 years sooner than people who do not have HIV. Low bone mineral density (BMD) is common in people with HIV. This means their risk of fractures is increased. People with …

NCT04964947 — Tobramycin Injection to Prevent Infection in Open Fractures

StatusActive, not recruiting
PhasePhase 3
SponsorMassachusetts General Hospital
Enrollment600
Study TypeINTERVENTIONAL
ConditionsWound Infection; Fractures, Open; Surgical Site Infection
Interventions

The goal of open extremity fracture (OEF) treatment is to promote fracture healing and restore function while preventing the development of infection. This is achieved through systematic and timely wound debridement and irrigation, fracture stabilization, tetanus prophylaxis, systemic and local antimicrobial therapy, and judicious timing of wound closure based on cleanliness. Early prophylactic…

NCT04616248 — In Situ Immunomodulation With CDX-301, Radiation Therapy, CDX-1140 and Poly-ICLC in Patients w/ Unresectable and Metastatic Solid Tumors

StatusActive, not recruiting
PhasePhase 1
SponsorUniversity of Southern California
Enrollment14
Study TypeINTERVENTIONAL
ConditionsAnatomic Stage IV Breast Cancer AJCC v8; Metastatic Breast Carcinoma; Prognostic Stage IV Breast Cancer AJCC v8; Unresectable Breast Carcinoma; Metastatic Melanoma
Interventions; ;

This phase I trial evaluates the safety and effectiveness of in situ immunomodulation with CDX-301, radiotherapy, CDX-1140 and Poly-ICLC (Cohort A) and these with intravenous (IV) pembrolizumab and subcutaneous (SC) tocilizumab (Cohort B) in treating patients with unresectable and measurable metastatic melanoma, cutaneous squamous cell carcinoma (SCC), basal cell carcinoma (BCC), Merkel cell ca…

Not Yet Recruiting

NCT07667153 — Myeloid Bias in the Bone Marrow of Septic Patients and Its Correlation With Disease Severity and Prognosis: A Single-Center, Prospective Cohort Study

StatusNot yet recruiting
PhaseN/A
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Enrollment45
Study TypeOBSERVATIONAL
ConditionsSepsis; Septic Shock
Interventions

Sepsis remains a leading cause of critical illness worldwide, yet the underlying mechanisms driving its profound and persistent immune dysfunction are incompletely understood. The bone marrow, as the birthplace of all immune cells, plays a central role in orchestrating systemic immune responses. Emerging evidence from animal models suggests that sepsis triggers emergency myeloid-biased hematopo…

NCT07240649 — Emerging Indications for Hyperbaric Oxygen Treatment

StatusNot yet recruiting
PhasePhase 4
SponsorJay C. Buckey Jr.
Enrollment100
Study TypeINTERVENTIONAL
ConditionsPost-COVID-19 Condition; Ulcerative Colitis; Crohn Disease; Calciphylaxis; Frostbite
Interventions;

This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The re…

NCT07668583 — EFFICACY AND SAFETY OF ZOLEDRONATE VERSUS PLACEBO ON PAIN AT WEEK 12 IN PEDIATRIC PATIENTS WITH CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS

StatusNot yet recruiting
PhasePhase 2
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment30
Study TypeINTERVENTIONAL
ConditionsOsteomyelitis Chronic
Interventions;

Chronic recurrent multifocal osteomyelitis (CRMO) is a rare auto-inflammatory bone disease that primarily affects children and/or adolescents at a median age of 10 years. Until now, there is no consensus regarding the treatment of CRMO. Non-steroidal anti-inflammatory drugs (NSAIDs) are considered the first line of therapy with remission in approximately 30% of cases. If unsuccessful, several t…

Completed Trials

NCT02812446 — Staphylokinase and ABO Group Phenotype: New Players in Staphylococcus Aureus Implant-associated Infections Development

StatusCompleted
PhaseN/A
SponsorNantes University Hospital
Enrollment88
Study TypeOBSERVATIONAL
ConditionsStaphylococcal Infection
Interventions;

The purpose of this study is to identify bacterial and/or clinical features involved in the pathogenesis of Staphylococcus aureus implant-associated infections (IAI). Materials & methods: In total, 57 IAI S. aureus and 31 nasal carriage (NC) S. aureus isolates were studied. Staphylococcus aureus genetic background was obtained by microarray analysis. Multilocus sequence typing was performed to…

NCT01224691 — TGF-(Beta) and Susceptibility to RSV

StatusCompleted
PhaseN/A
SponsorNational Institute of Environmental Health Sciences (NIEHS)
Enrollment113
Study TypeOBSERVATIONAL
ConditionsAsthma

Background:

  • Human respiratory syncytial virus (RSV) is a virus that causes respiratory tract infections, and is frequently responsible for hospital visits in infants and children. It can also trigger severe breathing problems for individuals who have asthma, but these infections are generally better tolerated in non-asthmatics. Some research suggests that lack of an efficient immune system r…

NCT03111745 — Retrospective Study of Viral Reactivation Across All Bone Marrow Transplant Protocols Since 2010

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment730
Study TypeOBSERVATIONAL
ConditionsViral Infections

Background:

Some blood and immune disorders can be helped with HSCT. This is allogeneic hematopoietic stem cell transplantation. The person who gets the stem cells has their immune system suppressed. This is done to help prevent their body from rejecting the transplant. During this time, the person is at a high risk to get viral infections. Researchers want to study the records of people who h…

NCT04576052 — Long-term Coated and Non-coated Tibia Nails

StatusCompleted
PhaseN/A
SponsorUniversity Hospital Muenster
Enrollment397
Study TypeOBSERVATIONAL
ConditionsImplant Infection

For this retrospective cohort study, medical records of patients treated between 2005 to 2019 with the UTN PROtect and/or ETN PROtect for tibia fractures or tibia revision cases will be examined. In comparison to this cohort, patients who received an uncoated tibia nail are examined as well. Demographics, pre-surgical health status, details on fracture type or on revision, treatment decision an…

NCT04530682 — COVID-19 in Rheumatic Inflammatory Diseases Under Immuno-suppressive Drugs

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment163
Study TypeOBSERVATIONAL
ConditionsChronic Inflammatory Rheumatism
Interventions

Accurate knowledge of the humoral immune responses induced by SARS-CoV-2 in patients undergoing immunosuppressive therapy is essential to guide recommendations for infected patients and for vaccination policy for uninfected immunosuppressed patients.

NCT05570656 — Modeling Spinal Mobility in Ankylosing Spondylitis: Towards New Telekinetic Biomarkers

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment40
Study TypeINTERVENTIONAL
ConditionsAnkylosing Spondylitis
Interventions

Ankylosing spondylitis (AS) is a chronic inflammatory rheumatic disease that mainly affects the spine and pelvis in its axial form. It is responsible for chronic inflammatory pain and sometimes ankylosis with significant functional retention.

Clinicians need markers capable of precisely measuring the restriction of range of motion in these patients, reflections of the activity and/or sequelae …

NCT07608523 — Marginal Bone Level Around Dental Implants in Periodontitis Patients

StatusCompleted
PhaseN/A
SponsorFaculty of Dental Medicine for Girls
Enrollment40
Study TypeINTERVENTIONAL
ConditionsPeriodontitis; Dental Implants; Marginal Bone Loss; Periodontal Probing Depth; Gingival Inflammation
Interventions;

This study evaluates and compares marginal bone level changes around dental implants with two different surface characteristics in patients with a history of periodontitis. Participants will receive dental implants and will be followed up for one year to assess bone level changes around the implants.

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment100
Study TypeOBSERVATIONAL
ConditionsInfection; Fracture; Bone
Interventions

The value of next-generation sequencing (NGS) using Nanopore technology has been demonstrated in the case of diabetic patients’ wounds or in prosthetic joint infections. The aim of this study is to demonstrate its relevance as a new diagnostic approach for fracture-related infections (FRI).

Bone samples from patient with FRI will be submitted to shotgun metagenomic Next-generation sequencing u…

NCT06526884 — Quasi-Randomized Evaluation of the UCLA Next Day Clinic (NDC)

StatusCompleted
PhaseN/A
SponsorUniversity of California, Los Angeles
Enrollment570
Study TypeINTERVENTIONAL
ConditionsPneumonia; Syncope; Congestive Heart Failure; Cellulitis; Pyelonephritis
Interventions

The Next Day Clinic (NDC) is a quality improvement initiative that will be launched and operated by UCLA Health starting July 22, 2024. Its goals are to improve patient care and safety and to maximize cost effectiveness. The way it does this is by identifying patients in the ED who would normally be admitted for low-acuity conditions, and diverting them to a high-acuity clinic the following day…

StatusCompleted
PhaseN/A
SponsorBoston Medical Center
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOpioid Use Disorder; Bloodstream Infection; Osteomyelitis; Endocarditis; Septic Arthritis
Interventions;

This project is a pilot study of an adapted intervention of an existing Opioid Use Disorder (OUD) treatment retention intervention called Recovery Management Checkups (RMC). This intervention has been adapted to better fit the experiences and unique issues of those that have been hospitalized with serious injection related infections (SIRI) based on the findings from a prior qualitative study f…

NCT07636265 — The Effect Of Photobiomodulation On Dental Implant Survival

StatusCompleted
PhasePhase 1
SponsorNigde Omer Halisdemir University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsImplant Complication; Periimplant Infection; Periimplant Bone Loss
Interventions

Dental implants offer a high success rate as the most up-to-date treatment method for replacing lost teeth. However, whilst implants have emerged as the ideal treatment for tooth loss, the incidence of postoperative complications-including postoperative oedema, wound infection, and early dehiscence or perforation of the soft tissue flap-has also increased. The soft tissue surrounding the implan…

Other (Terminated)

NCT04067219 — SkIn, Muscle and Bone Aging Determinants in HIV Infected-patients.

StatusTerminated
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment123
Study TypeINTERVENTIONAL
ConditionsHIV-1-infection; Marker; Structural
Interventions

this study consists of the study of markers of skin, muscular, neurocognitive and bone aging in HIV infected adults and to compare the frequency of these signs to the general population of same gender and age.

NCT01962636 — Umbilical Cord Blood Transplantation Using a Myeloablative Preparative Regimen for Hematological Diseases

StatusTerminated
PhaseN/A
SponsorMasonic Cancer Center, University of Minnesota
Enrollment200
Study TypeINTERVENTIONAL
ConditionsAcute Myeloid Leukemia (AML); Acute Lymphocytic Leukemia (ALL); Chronic Myelogenous Leukemia; Plasma Cell Leukemia; Myelofibrosis
Interventions; ;

This is a treatment guideline for an unrelated umbilical cord blood transplant (UCBT) using a myeloablative preparative regimen for the treatment of hematological diseases, including, but not limited to acute leukemias. The myeloablative preparative regimen will consist of cyclophosphamide (CY), fludarabine (FLU) and fractionated total body irradiation (TBI).

NCT03226821 — Body Composition and Adipose Tissue in HIV

StatusTerminated
PhasePhase 4
SponsorColumbia University
Enrollment6
Study TypeINTERVENTIONAL
ConditionsHIV Lipodystrophy Syndrome; Growth Hormone Deficiency; Body Composition
Interventions

In this study, the investigators will examine the effect of therapy with the Growth Hormone Releasing Hormone (GHRH) analog tesamorelin on body composition in patients with HIV lipodystrophy and central adiposity. This study is a single arm prospective study of tesamorelin therapy of patients with HIV lipodystrophy. Subjects will do body composition testing, adipose tissue biopsy, metabolic rat…

Other (Suspended)

NCT07684014 — Evaluation of Bone Healing After Obturation With Dia-Root Bio Sealer (Calcium Silicate-based Sealer CSBS) Using Three Obturation Techniques

StatusSuspended
PhaseN/A
SponsorAin Shams University
Enrollment63
Study TypeINTERVENTIONAL
ConditionsPeriapical Periodontitis; Chronic Periapical Periodontitis; Periapical Abscess; Pulp Necrosis, Apical Periodontitis; Pulp Necrosis
Interventions; ;

The study aims to evaluate the efficiency of using a Calcium silicate-based sealer (CSBS) with different obturation techniques in treating root canals with apical periodontitis in single visit.

Evaluating:

  1. Postoperative healing.
  2. Preoperative, postoperative pain and frequency of analgesic intake.