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 Sinusitis from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 14
- Active, not recruiting: 9
- Completed: 15
- Other: 12
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT02038166 — Nasal Potential Difference (NPD) Protocol in Chronic Rhinosinusitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Rhinosinusitis |
The purpose of this study is to determine if acquired (partial) Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) deficiency contributes substantially to the pathogenic mechanisms underlying Chronic Rhinosinusitis (CRS), creating a localized environment that impairs mucociliary clearance (MCC).
NCT02975310 — In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ottawa Hospital Research Institute |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis; Nasal Polyps |
| Interventions | ; ; |
Chronic rhinosinusitis, also called chronic sinusitis, is a very common life-long disease affecting over 5% of the Canadian population. Its symptoms, including daily facial pain and headache, an inability to breath through the nose and complete smell loss, regularly impair one’s ability to work and to enjoy and participate in daily activities. The annual cost of chronic sinusitis to Canada is e…
NCT06130176 — Single-step Functional Sinus Endoscopy and Transoral Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Qassim University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Maxillary Sinusitis |
| Interventions | ; ; |
Dento- alveolar or dental structural diseases that affect the floor of the maxillary sinus can cause maxillary sinusitis which is known as odontogenic maxillary sinusitis (OMS). Many treatment protocols have been documented to treat OMS. However, There is no unanimity among clinicians on how and who should treat OMS, whether is it otolaryngologist, oral/maxillofacial surgeons, or dentist. There…
NCT05547633 — Detection and Management of Sinusitis in a Single-center Prospective Cohort of Patients With Exudative AMD (SINE)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fondation Ophtalmologique Adolphe de Rothschild |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | AMD |
| Interventions |
An inflammatory component associated with AMD has been highlighted by genetic associations of predisposition to AMD, as well as by the recently demonstrated link between AMD and periodontitis.
Some patients followed at the Fondation Adolphe de Rothschild Hospital for wet AMD seemed to show an improvement of neovascular activity (less need for intravitreal injections of anti-VEGF) after treatme…
NCT06076304 — Nasal Steroids, Irrigation, Oral Antibiotics, and Subgroup Targeting for Effective Management of Acute Sinusitis
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Daniel Merenstein |
| Enrollment | 3720 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinus Infection; Acute Sinusitis |
| Interventions | ; ; |
Sinus infections (also called acute rhinosinusitis or ARS) affect about 15% of adults each year, and are one of the top reasons people receive antibiotics in outpatient settings. Since most sinus infections are caused by viruses, many patients who take antibiotics for this condition do not actually benefit. Even though this has decreased over recent years, 70% of people are still prescribed the…
NCT06439381 — Long-term Safety and Efficacy of TQH2722 Injection in the Treatment of Chronic Sinusitis With or Without Nasal Polyps
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis |
| Interventions |
This is a multicenter, randomized, continuing, Phase II expansion trial to evaluate the safety, efficacy, and immunogenicity of two doses of TQH2722 in the long-term treatment of severe chronic sinusitis with or without nasal polyps.
NCT06023550 — Complicated Infections in Otorhinolaryngology
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Medical Centre Ljubljana |
| Enrollment | 2550 |
| Study Type | OBSERVATIONAL |
| Conditions | Sinusitis; Otitis; Laryngitis; Lymphadenitis; Quinsy |
| Interventions |
This observational study aims to learn more about complicated infections treated by otorhinolaryngologists. The main questions to answer are:
- What is the management of complicated sinonasal infections in Ljubljana, Slovenia,
- What is the management of complicated ear and temporal bone infections in Ljubljana, Slovenia,
- What is the management of complicated neck soft tissue infections in L…
NCT05427695 — Topical Probiotic Sinus Irrigations for Treating Chronic Sinusitis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University of Illinois at Chicago |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis (Diagnosis) |
| Interventions | ; |
The purpose of this randomized study will be to determine whether topical probiotic sinus irrigations are more effective compared to saline sinus irrigation controls in the treatment of active CRS in patients who have had prior sinus surgery based on subjective and objective outcome measures.
NCT06901297 — The Efficacy and Safety of Raphamin in the Treatment of Acute Rhinosinusitis in Adult Patients
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Materia Medica Holding |
| Enrollment | 552 |
| Study Type | INTERVENTIONAL |
| Conditions | Rhinosinusitis; Rhinosinusitis Acute |
| Interventions | ; |
Multicenter double-blind placebo-controlled randomized in parallel groups clinical trial of the efficacy and safety of Raphamin in the treatment of acute rhinosinusitis in adult patients.
NCT06850805 — Efficacy and Safety of 186 mcg of OPN-375 Nasal Spray Twice a Day (BID) in Adolescents With Chronic Rhinosinusitis Without Nasal Polyps
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Optinose US Inc. |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis Without Nasal Polyps |
| Interventions | ; |
This is a 12-Week randomized, double-blind, placebo-controlled, parallel-group, multicenter study evaluating the efficacy and safety of intranasal administration of 186 µg of OPN-375 twice a day (BID) in adolescent subjects with chronic rhinosinusitis without nasal polyps. The total planned number of subjects is approximately 84 adolescents (12-17 years of age) who will be randomly assigned to …
NCT07107256 — Clinical Trial of TQC2731 Injection in Patients With Chronic Sinusitis and Nasal Polyps
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd. |
| Enrollment | 246 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) |
| Interventions | ; |
TQC2731 injection is a humanized monoclonal antibody that targets Thymic Stromal Lymphopoietin (TSLP), blocks the TSLP pathway, and inhibits the production of downstream cytokines, thereby exerting anti-inflammatory effects. The purpose of this study is to evaluate the efficacy and safety of TQC2731 injection in patients with chronic rhinosinusitis with nasal polyps (CRSwNP).
NCT07359287 — Impact of a Multimodal Intervention on Antibiotic Prescribing for Respiratory Infections in Primary Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Caen |
| Enrollment | 4500 |
| Study Type | INTERVENTIONAL |
| Conditions | Angina; Acute Bronchiolitis; Acute Bronchitis; COPD Exacerbation (AECOPD); Laryngitis |
| Interventions |
Antimicrobial resistance (AMR), considered one of the greatest global threats by the WHO, justifies the development of initiatives to promote appropriate antibiotic use-especially in primary care, where most antibiotics in France are prescribed and where misuse remains common.
We are proposing a cluster-randomized controlled trial to evaluate the effectiveness of a bimodal intervention combini…
NCT07383493 — RhinAV_Evaluation of Treatments for Acute Viral Rhinitis, Rhinosinusitis, and Rhinopharyngitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Rhinitis Acute; Rhinitis Viral; Rhinosinusitis Acute; Rhinopharyngitis; Rhinitis |
| Interventions | ; ; |
The objective of this study is to conduct post-marketing clinical follow-up of four products: NS, NHE, NHG, and PIR. This follow-up will consist of collecting clinical data in real-life conditions to confirm the tolerance, safety, and efficacy of medical devices used in the treatment of acute viral rhinitis, rhinosinusitis, and rhinopharyngitis, while also assessing the benefit/risk ratio of th…
NCT06824649 — Biologics in Chronic Rhinosinusitis With Nasal Polyposis
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Medical University of South Carolina |
| Enrollment | 504 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Sinusitis; Nasal Polyps |
| Interventions |
The prevalence of Chronic Sinusitis with Nasal Polyps (CRSwNP) in the United States is estimated at roughly 4%, which equates to over 13 million Americans. Until recently, the only medical treatment options available for patients with CRSwNP were corticosteroids, with surgery reserved for medical failure. The development of biologic medications over the last 5 years has revolutionized the treat…
Active, Not Recruiting
NCT00880516 — Genetic Factors in Chronic Sinusitis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 1200 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Sinusitis |
The purpose of this study is to learn more about the genetics of chronic sinusitis and identify genes involved in chronic sinusitis.
NCT02533206 — Pilot Study of The EPIC Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ottawa Hospital Research Institute |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis; Nasal Polyps |
| Interventions | ; |
Chronic sinusitis is one of the most common chronic diseases in North America, with over 5% of the Canadian population affected by the disease. Until now, treatment with surgery has been performed only in the operating room. Recently a smaller surgical procedure that is done in the clinic for some patients with chronic sinusitis with polyps has been found to result in symptom control that appea…
NCT03256773 — High Resolution Micro OCT Imaging
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 160 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; COPD; PCD - Primary Ciliary Dyskinesia; Covid19; Sinusitis |
The purpose of this study is to learn about using the imaging to make images of the lungs and nose with the long-term goal of the research leading to potential treatments and new therapies for patients with cystic fibrosis.
NCT05454072 — Microbiota Transfer for Chronic Rhinosinusitis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Amin Javer |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis, Chronic; Sinus Disease; Sinus Infection; Sinus Infection Chronic |
| Interventions | ; |
Chronic sinusitis (CRS) is a common inflammatory condition of the sinuses that affects up to 2.5% of the Canadian population, and is thought to be caused by bacterial infection, resistant biofilms, chronic inflammation and possibly an unhealthy population of sinus microbes (or microbiota). Symptoms include nasal obstruction and discharge, facial pain, loss of smell and sleep disturbance, which …
NCT06516302 — A Study of GR1802 in Participants With Chronic Sinusitis With Nasal Polyps
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Genrix (Shanghai) Biopharmaceutical Co., Ltd. |
| Enrollment | 228 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis With Nasal Polyps |
| Interventions | ; |
The goal of this clinical trial is to learn if GR1802 works to treat severe chronic rhinosinusitis with nasal polyps (CRSwNP) in adults. It will also learn about the safety of GR1802. The main questions it aims to answer are:
- Does GR1802 reduce the need for surgery and systemic corticosteroid use?
- What medical problems do participants have when taking GR1802?
Researchers will compare GR…
NCT06639295 — A Study to Evaluate 611 in Patients With Chronic Rhinosinusitis With Nasal Polyps
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. |
| Enrollment | 243 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis; Nasal Polyps |
| Interventions | ; |
This study will evaluate the effect and safety of 611 in patients with Chronic Rhinosinusitis with Nasal Polyps (CRSwNP)
NCT06706817 — A Study to Investigate Changes in Symptoms in Adult Participants With Chronic Rhinosinusitis With Nasal Polyposis Initiating Treatment With Tezepelumab
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 181 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis With Nasal Polyps |
| Interventions |
The main objective of this study is to evaluate treatment outcomes of tezepelumab among participants with physician-determined surgery-eligible CRSwNP, with or without asthma.
Study details include:
- The study duration will be up to 40 weeks.
- The treatment duration will be up to 24 weeks.
- The visit frequency will be once every 4 weeks (Q4W).
NCT07217002 — Reducing Antibiotic Use by Implementation of Stewardship in Primary and Urgent Care
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 420 |
| Study Type | OBSERVATIONAL |
| Conditions | Community Acquired Pneumonia (CAP); Sinusitis; Strep Pharyngitis; Acute Otitis Media (AOM) |
| Interventions | ; ; |
The goal of this project is to reduce unnecessary antibiotic use for children with ARTIs (Acute Respiratory Tract Infections) by implementing “outpatient antibiotic stewardship” across the Children’s Hospital of Philadelphia (CHOP) Primary and Urgent Care Network to:
- Reduce unnecessary antibiotic prescribing for the most common infections in children.
- Reduce unnecessary a) broad-spectrum…
NCT07015736 — Effects of Saccharomyces Boulardii CNCM I-745 on Antibiotic-Associated Perturbation in Children Treated for Acute Respiratory Infections (RESTORE Study)
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Eskisehir Osmangazi University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Antibiotic Associated Diarrhea; Acute Otitis Media; ACUTE SINUSITIS |
| Interventions | ; |
This study aims to evaluate the effect of co-administering the probiotic Saccharomyces boulardii CNCM I-745 with amoxicillin-clavulanic acid on the intestinal and nasopharyngeal microbiota in children diagnosed with acute otitis media or acute bacterial sinusitis. The trial will also assess the potential of the probiotic to reduce antibiotic-associated diarrhea (AAD), antibiotic associated micr…
Not Yet Recruiting
NCT07257224 — Post-market Clinical Follow-up Study of an Isotonic Saline Solution to Manage Nasal Congestion in Case of Flu Symptoms, Colds, Allergic Rhinitis and Rhinosinusitis in Infants and Toddlers
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Laboratoires Quinton International S.L. |
| Enrollment | 83 |
| Study Type | OBSERVATIONAL |
| Conditions | Nasal Congestion; Common Cold; Allergic Rhinitis; Rhinosinusitis; Flu Symptom |
| Interventions |
The goal of this observational post-market clinical follow-up study is to evaluate the safety and performance of the CE-marked nasal spray in the management of nasal congestion in case of flu, colds, allergic rhinitis and rhinosinusitis in infants and toddlers aged 3 to 48 months at day 5 post-enrolment. Enrolment does not require establishing a medical diagnosis; eligibility is based on guardi…
NCT07408869 — A Phase 1 Study of Cizutamig in IgE Mediated Diseases
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Candid Therapeutics |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | IgE-Mediated Hypersensitivity; IgE Mediated Food Allergy; IgE-Mediated Cow Milk Allergy |
| Interventions |
The purpose of this study is to evaluate the pharmacodynamics, safety, tolerability, pharmacokinetics, and immunogenicity of cizutamig in IgE Mediated Diseases.
NCT07151313 — Efficacy of Bee Venom Phonophoresis in Treating Chronic Sinusitis:
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sinai University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Sinusitis; Acute Sinusitis; Rhinosinusitis |
| Interventions | ; ; |
This double-blind, randomized controlled trial (BEE-SONIC) aims to evaluate the efficacy of bee venom phonophoresis in the treatment of chronic sinusitis. Thirty adult patients (aged 18-65 years) with clinically diagnosed chronic or acute sinusitis will be randomized into two groups: the intervention group will receive bee venom phonophoresis using low-to-moderate intensity ultrasound, while th…
NCT07635433 — Thermosensitive Gel Nasal Spray With Stem Cell Exosomes, Mupirocin, and DNase I for Chronic Sinusitis
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | The First Affiliated Hospital of Xinxiang Medical College |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis With Nasal Polyps |
| Interventions | ; ; |
This study tests a new nasal spray for adults (18-65 years) with chronic rhinosinusitis (CRS) without nasal polyps. The spray contains a temperature-sensitive gel (thermosensitive gel) that turns into a soft gel inside the nose to slowly release three active ingredients: human umbilical cord mesenchymal stem cell exosomes (hUC-MSC-Exo) to help heal the nasal lining, mupirocin (an antibiotic tha…
NCT07635459 — Thermosensitive Gel Nasal Spray With Exosomes, Azelastine, and Interferon for Acute Phase of Chronic Sinusitis
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | The First Affiliated Hospital of Xinxiang Medical College |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Rhinosinusitis Without Polyps |
| Interventions | ; ; |
This study tests a new nasal spray for adults (18-65 years) with chronic sinusitis experiencing an acute phase. The spray contains a temperature-sensitive gel that turns into a soft gel inside the nose to slowly release three active ingredients: stem cell exosomes (to repair nasal lining), azelastine (an antihistamine and anti-inflammatory drug), and interferon alpha-2b (an antiviral agent). Th…
NCT07620522 — Observational Study of RHINOSEDAL in Acute Nasal Obstruction
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Laboratoires Elerte |
| Enrollment | 126 |
| Study Type | OBSERVATIONAL |
| Conditions | Nasal Obstruction; Common Cold; Allergic Rhinitis; Non-allergic Rhinitis; Rhinosinusitis |
| Interventions |
This prospective, multicenter, national, observational, non-interventional post-market clinical follow-up study evaluates the performance and safety of RHINOSEDAL in children and adults presenting with acute nasal obstruction associated with common cold, allergic or non-allergic rhinitis, or rhinosinusitis. Patients prescribed RHINOSEDAL in routine care will be followed for 6 ±1 days using pati…
Enrolling by Invitation
NCT06603935 — Harnessing Digital Medicine to Improve Allergic Rhinitis Management in Primary Care (DMAR)
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | QHSLab, Inc. |
| Enrollment | 240 |
| Study Type | INTERVENTIONAL |
| Conditions | Allergic Rhinitis; Sinusitis |
| Interventions |
This study aims to evaluate the effectiveness of digital tools in managing allergic rhinitis (AR) in primary care settings. AR is a common condition that affects many people’s quality of life. The study will test whether digital tools, such as the QHSLab platform, can help patients better control their symptoms, improve adherence to treatment, and enhance overall well-being. The trial will comp…
NCT07383350 — Improving Patient-centered Communication and Antibiotic Use With Information Sheets for Acute Respiratory Tract Infections: A Study Protocol
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Research Unit for General Practice in Aalborg |
| Enrollment | 1144 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Bronchitis; ACUTE SINUSITIS; Sore Throat |
| Interventions |
The goal of this trial is to investigate if the use of information sheets regarding acute respiratory tract infections will lead to more rational antibiotic prescribing and increase patient-centered communication i Danish general practice.
The main questions to be answered:
- Will the use of information sheets lower antibiotic prescribing.
- Will the use of information sheets increase patient…
NCT07149428 — Longitudinal Deep Phenotyping of Central Mechanisms in Dysosmia: A Pilot Study Using Electrobulbogram (EBG), Functional MRI (fMRI), and Diffusion-Weighted Imaging (DWI)
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Institute on Deafness and Other Communication Disorders (NIDCD) |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Respiratory Tract Infection; Smell Disorder; Influenza; Rhinosinusitis; COVID-19 |
Background:
Loss of the sense of smell can seriously affect a person’s quality of life. The ability to smell can be damaged by many factors, including illnesses, injuries, and exposure to toxic chemicals. The effects can vary, including complete loss of smell, partial loss, and parosomia, which is when things smell differently than they should.
Objective:
To study how brain function changes …
Completed Trials
NCT01684540 — Application of Ectoin® Rhinitis Nasal Spray in Patients With Acute Rhinosinusitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Bitop AG |
| Enrollment | 66 |
| Study Type | OBSERVATIONAL |
| Conditions | Sinusitis |
| Interventions | ; |
This is a comparative, open label, parallel group, non interventional study to further demonstrate the effectiveness and tolerability of Ectoin® Rhinitis Nasal Spray. In addition the effectiveness and safety shall be compared to a Sinupret forte. The patient applies Ectoin® Rhinitis Nasal Spray or takes Sinupret forte according to the instructions for use. The observation takes place over a per…
NCT02972281 — Systematic Search for Primary Immunodeficiency in Adults With Infections
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Lille |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Complement Deficiency; Antibody Deficiency; Chronic Sinus Infection; Meningitis, Bacterial; Pneumonia, Bacterial |
| Interventions |
Antibody deficiencies and complement deficiencies are the most frequent Primary immunodeficiencies (PIDs) in adults, and are associated with greatly increased susceptibility to recurrent and/or severe bacterial infections - especially upper and lower respiratory tract infections and meningitis. The literature data suggest that PIDs are under-diagnosed in adults. The current European and US guid…
NCT06687629 — Best Practice in the Management of Concha Bullosa in FESS Operation
| Status | Completed |
| Phase | N/A |
| Sponsor | Helsinki University Central Hospital |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis; Sinusitis Bacterial; Sinusitis Recurrent; Turbinate; Hypertrophy Mucous Membrane; Turbinate Hypertrophy |
| Interventions | ; |
Concha bullosa (CB) refers to the condition where the middle turbinate’s interior is aerated (making the turbinate wide and thick). CB can narrow the middle meatus and the ostiomeatal complex. In adults suffering from chronic sinusitis, the prevalence of CB is approximately 34%. The most common treatment method for CB is turbinate crushing. This is considered a conservative treatment that prese…
NCT04187976 — Eosinophils Endotypes in Chronic Airway Inflammatory Diseases
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Lille |
| Enrollment | 70 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Asthma; Chronic Sinusitis; Eosinophilic Rhinitis |
Asthma and chronic rhinosinusitis with nasal polyps (CRSwNP) are frequently described as unified airway inflammatory diseases. Both heavily impacts quality of life with substantial productivity loss. They share the same pathophysiologic pattern based upon proTh2 immune response with blood eosinophils recruitment. Eosinophils are the major actor of persistent mucosal inflammation by promoting th…
NCT04684524 — Dupilumab in Allergic Fungal Rhinosinusitis (AFRS) (LIBERTY-AFRS-AI)
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Sanofi |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Allergic Fungal Rhinosinusitis |
| Interventions | ; |
Primary Objective:
- To evaluate the efficacy of treatment with dupilumab to reduce sinus opacification in a population with allergic fungal rhinosinusitis (AFRS)
Secondary Objectives:
- To evaluate the efficacy of treatment with dupilumab to reduce sinus opacification in a population with allergic fungal rhinosinusitis (AFRS) at Week 24
- To assess the efficacy of dupilumab to reduce the ne…
NCT04970966 — Efficacy of PuraSinus Versus Bioresorbable Nasal Dressings
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Southern California |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Sinus Disease; Surgery |
| Interventions | ; |
Postoperative care of patients undergoing endoscopic sinus surgery (ESS) is important both to minimize discomfort for the patients and to obtain the optimal long-term outcomes. Postoperative sinonasal cavity debridement has been advocated to prevent potential synechiae and sinus ostial stenosis, as well as to improve patient symptoms. Removal of old blood, nasal secretions, crusting, and unabso…
NCT05295459 — Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis in Adults (ENLIGHTEN 2)
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Lyra Therapeutics |
| Enrollment | 182 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Sinusitis; Chronic Rhinosinusitis (Diagnosis) |
| Interventions | ; ; |
Multicenter, phase III, randomized, blinded, controlled, parallel group.
NCT05127161 — Broad Implementation of Outpatient Stewardship
| Status | Completed |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 1032 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Respiratory Tract Infection; Otitis Media; Pharyngitis; Acute Sinusitis |
| Interventions |
Reducing inappropriate antibiotic use is a key strategy to mitigate antibiotic resistance and adverse health effects associated with antibiotic exposure. The Broad Implementation of Outpatient Stewardship (BIOS) project focuses on broadly implementing an evidence-based intervention to improve antibiotic prescribing for acute respiratory tract infections in pediatric outpatient settings. Primary…
NCT06264141 — Evaluation of Nitric Oxide Nasal Spray (NONS) for Treatment of Recurrent Acute Rhinosinusitis
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Sanotize Research and Development corp. |
| Enrollment | 162 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Acute Rhinosinusitis |
| Interventions | ; |
A two-week therapy of nitric oxide nasal spray (NONS) vs Placebo (saline nasal spray) initiated immediately after the onset of a new Recurrent Acute Rhinosinusitis (RARS) episode to assess the acceleration to clinical success (cured/much improved symptoms), lack of use of intranasal corticosteroids (INCS) (Day 5, or thereafter) and rescue oral antibiotics (ATBs) (Day 8, or thereafter) after ini…
NCT07560254 — Clinical Outcomes and Patient Satisfaction With Velnez Versus Nasopore in Nasal Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | Ayu, Inc. |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Rhinosinusitis; Sinusitis; Chronic Rhino-sinusitis |
| Interventions | ; |
This clinical trial evaluated two absorbable nasal packing materials - VELNEZ and NASOPORE - in adult patients (18-70 years) who underwent nasal surgery, including septoplasty, FESS, or turbinoplasty.
The study addressed two core questions: whether VELNEZ offered superior haemorrhage control and faster biodegradation, and whether it reduced postoperative pain, fibrosis, adhesion, and discomfor…
NCT07542444 — Craniosacral Osteopathic Treatment for Chronic Sinusitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Alanya Alaaddin Keykubat University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Craniosacral Osteopathic Manipulation; Chronic Sinusitis; Physiotherapy and Rehabilitation; Ear,Nose and Throat Surgery |
| Interventions | ; |
Chronic rhinosinusitis (CRS) is a common inflammatory condition that significantly impairs quality of life and is often insufficiently managed with standard medical therapy alone. Emerging evidence suggests that manual therapy approaches, including osteopathic manipulative treatment, may provide additional clinical benefits by improving lymphatic drainage, modulating autonomic function, and enh…
NCT07675512 — Adelmidrol in Chronic Sinusitis
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Campania Luigi Vanvitelli |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Sinusitis With Nasal Polyps |
| Interventions | ; ; |
The goal of this study is to evaluate whether a nasal spray containing adelmidrol, a mast cell modulator and precursor of palmitoylethanolamide, can reduce inflammation, improve symptoms, and decrease nasal polyp size in patients with chronic rhinosinusitis with nasal polyps. The study will also assess whether adelmidrol can improve surgical outcomes and potentially reduce the need for surgery …
NCT06661252 — Evaluation of Nasal Biomarkers for Objective Assessment of Disease Severity in Respiratory Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | Diag-Nose Medical Pty Ltd |
| Enrollment | 111 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease (COPD); Asthma Patients; Asthma and Rhinitis; Asthmatic Patients; Asthma, Chronic Obstructive Pulmonary Disease (COPD) |
| Interventions |
This research study is an observational, single site study quantifying expression of biomarkers of respiratory disease in nasal fluid using the ABEL microsampler device. The primary objective of this study is to compare biomarker expression between healthy controls and participants with respiratory disorders such as chronic obstructive pulmonary disorder (COPD), hayfever, chronic sinusitis, ast…
NCT07542275 — Endoscopic Assessment of Schneiderian Membrane Perforation During Osseodensification-mediated Transcrestal Sinus Floor Elevation With Graftless Immediate Implant Placement in Subsinus Bone Height of 4-6 mm: A Pilot Study.
| Status | Completed |
| Phase | N/A |
| Sponsor | Saint-Joseph University |
| Enrollment | 6 |
| Study Type | INTERVENTIONAL |
| Conditions | Sinusitis; Periodontal Disease |
| Interventions |
This present study will evaluate Schneiderian membrane perforation rates using osseodensification in TSFE with simultaneous graftless implant placement, under sinuscopic control monitored by an ENT specialist.
An endoscopic evaluation will be continuously conducted throughout the surgical procedure. TSFE will be performed using Densah burs without the addition of bone graft material, followed …
NCT07534280 — Herbal Tea Extract for Management of Rhinosinusitis
| Status | Completed |
| Phase | N/A |
| Sponsor | Deraya University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Rhino Sinusitis |
| Interventions | ; ; |
The objective of this phase I controlled clinical trial is to determine the safety and efficacy of Berry leaves & Mango leaves mixture in symptomatic treatments on disease-related quality of life in adults with clinically diagnosed acute rhinosinusitis. Ten adult subjects, 18 to 70 years old, who meet the recommended criteria for acute rhinosinusitis, will be enrolled from Minia university ENT…
Other (Terminated)
NCT02509663 — Treatment of Chronic Frontal Sinusitis by a Simple Technique Using Dilation Balloons
| Status | Terminated |
| Phase | N/A |
| Sponsor | University Hospital, Strasbourg, France |
| Enrollment | 9 |
| Study Type | INTERVENTIONAL |
| Conditions | Frontal Sinusitis |
| Interventions | ; ; |
The sinuplasty balloon offers a more physiological first of the sinuses which minimizes risks associated to traditional surgery. Its atraumatic characteristic also helps to reduce the risk of bleeding (so any use of Pack), limit scarring ransom, reduce the post-operative pain, ensure faster return to daily life activities (reduction of the average length of hospitalization). Patient’s quality o…
NCT04085536 — Prospective Study on the Efficacy of Exclusive Odontological and Medical Treatment in Chronic Dental Maxillary Sinusitis
| Status | Terminated |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal Creteil |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Maxillary Sinusitis |
| Interventions |
The study will be offered to patients for whom chronic maxillary sinusitis will be diagnosed in the first ENT (ear, nose and throat) consultation. These patients will then be seen in a stomatology consultation to determine whether or not a dental cause is objective
Other (Withdrawn)
NCT05454163 — Post-radiotherapy Rhinosinusitis in Children
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | University Hospital, Lille |
| Enrollment | N/A |
| Study Type | OBSERVATIONAL |
| Conditions | Pediatric Cancer; Chronic Sinusitis |
| Interventions |
Chronic rhinosinusitis (CRS) is a frequent complication of facial cancer treatment, mainly related to radiotherapy. However, while radiological involvement is frequent, clinical expression seems less important.
Few studies have investigated the incidence of this condition in the pediatric population while its evolution seems to be very chronic even if a partial improvement may occur with time….