Clinical Trials for Eye Infections

Currently registered clinical trials for Eye Infections from ClinicalTrials.gov. 22 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 Eye Infections from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 22
  • Active, not recruiting: 4
  • Completed: 15
  • Other: 9

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

Recruiting Trials

NCT00005917 — Study of Chediak-Higashi Syndrome

StatusRecruiting
PhaseN/A
SponsorNational Human Genome Research Institute (NHGRI)
Enrollment60
Study TypeOBSERVATIONAL
ConditionsChediak-Higashi Syndrome

Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder characterized in its classical form by oculocutaneous albinism, a bleeding diathesis, recurrent infection due to abnormal neutrophil and natural killer cell function, and eventual progression to a lymphohistiocytic infiltration known as the accelerated phase . Death often occurs within the first decade as a result of infectio…

NCT03059420 — Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies

StatusRecruiting
PhaseN/A
SponsorBoston Children’s Hospital
Enrollment20000
Study TypeOBSERVATIONAL
ConditionsCongenital Fibrosis of Extraocular Muscles; Duane Retraction Syndrome; Duane Radial Ray Syndrome; Mobius Syndrome; Brown Syndrome

The purpose of this study is to identify genes associated with impaired development and function of the cranial nerves and brainstem, which may result in misalignment of the eyes (strabismus) and related conditions.

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.

NCT02357238 — Genetics of Uveitis

StatusRecruiting
PhaseN/A
SponsorThe Cleveland Clinic
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsUveitis; Infectious Uveitis

In order to improve the investigators knowledge about uveitis and the underlying mechanism of disease, the investigators propose collecting blood from patients with uveitis, isolating DNA and sequencing the DNA to identify genetic mutations or associations in these patients.

NCT04198740 — Proteomic and Metabolomic Lacrimal Fingerprint in Diverse Pathologies of the Ocular Surface

StatusRecruiting
PhaseN/A
SponsorCentre hospitalier de l’Université de Montréal (CHUM)
Enrollment300
Study TypeOBSERVATIONAL
ConditionsDry Eye Syndrome; Infectious Keratoconjunctivitis; Mucous Membrane Pemphigoid; Allergic Conjunctivitis
Interventions

This study aims to obtain the lacrimal fingerprint for frequent pathologies of the ocular surface and establish a normative base for each of them.

NCT04402086 — Rheumatology Patient Registry and Biorepository

StatusRecruiting
PhaseN/A
SponsorYale University
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsRheumatic Diseases; Adult Onset Still Disease; Ankylosing Spondylitis; Psoriatic Arthritis; Reactive Arthritis

To facilitate clinical, basic science, and translational research projects involving the study of rheumatic diseases.

NCT05414994 — Assessment of the Ocular Microbiome in Health and Disease

StatusRecruiting
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment500
Study TypeOBSERVATIONAL
ConditionsMicrobial Colonization; Eye Diseases; Ophthalmopathy
Interventions

The objective of this application is to illustrate the core constituents of the ocular surface microbiome, describe factors that promote colonization, and assess the ocular microbiome’s role in the health of the anterior segment. We will conduct a prospective, observational cohort study, including a longitudinal analysis of the ocular microbiome in adults.

NCT07634913 — Development of a Mobile Terminal-Based Intelligent Detection System for Multiple Anterior Segment Diseases of the Eye

StatusRecruiting
PhaseN/A
SponsorZhongshan Ophthalmic Center, Sun Yat-sen University
Enrollment3000
Study TypeOBSERVATIONAL
ConditionsArtifical Intelligence; Cataract; Pterygium; Keratopathy; Subconjunctival Hemorrhage
Interventions

This is a multi-center, cross-sectional study evaluating a smartphone-based artificial intelligence (AI) system for anterior segment eye disease screening. The system is designed to identify 16 clinically important anterior segment conditions from images captured using a standard Android smartphone. A core design feature of the system is that all image analysis is performed entirely on the smar…

NCT06213649 — Parasitic Ulcer Treatment Trial

StatusRecruiting
PhasePhase 3
SponsorJeremy Keenan, MD, MPH
Enrollment232
Study TypeINTERVENTIONAL
ConditionsAcanthamoeba Keratitis
Interventions; ;

The Parasitic Ulcer Treatment Trial (PUTT) is a multi-center, parallel-group, randomized clinical trial. The purpose of this study is to determine whether including topical corticosteroids in a regimen for acanthamoeba keratitis (AK) will improve vision. Patients presenting to all enrollment centers with evidence of acanthamoeba keratitis will be eligible for the trial if there is evidence of o…

NCT06023550 — Complicated Infections in Otorhinolaryngology

StatusRecruiting
PhaseN/A
SponsorUniversity Medical Centre Ljubljana
Enrollment2550
Study TypeOBSERVATIONAL
ConditionsSinusitis; 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…

NCT06911424 — Efficacy of Fusidic Acid 1% in the Treatment of Bacterial Conjunctivitis

StatusRecruiting
PhasePhase 3
SponsorBaxis Pharmaceuticals, Inc.
Enrollment400
Study TypeINTERVENTIONAL
ConditionsBacterial Conjunctivitis
Interventions;

The purpose of this clinical trial is to demonstrate the superiority of fusidic acid 1% over placebo in adults and children with confirmed bacterial conjunctivitis and to further establish the safety profile of fusidic acid 1% for topical ocular administration.

NCT06895902 — Suture Lid Spring for Lid Closure in Patients With Facial Nerve Palsy

StatusRecruiting
PhaseEarly Phase 1
SponsorUniversity of Alberta
Enrollment10
Study TypeINTERVENTIONAL
ConditionsFacial Nerve Palsy; Corneal Exposure; Paralytic Lagophthalmos
Interventions

The eyelids protect the cornea and eyelid closure is essential to ocular health and clear vision.

Patients with permanent Bells palsy or facial nerve palsy from other reasons such as tumours or trauma may be unable to blink and protect their cornea.

Irreversible visual loss can occur if the cornea is not kept lubricated.

Current treatment options for patients whose eyelid blink does not reco…

NCT07070843 — Effects of Two Different Eye Care Practices on Eye Complications in Mechanically Ventilated Intensive Care Patients

StatusRecruiting
PhaseN/A
SponsorIstanbul Saglik Bilimleri University
Enrollment156
Study TypeINTERVENTIONAL
ConditionsEye Care; Nursing Care; Intensive Care Unit
Interventions; ;

This study was designed as a prospective, randomized controlled experimental study aiming to compare different approaches to eye care in intensive care patients receiving mechanical ventilation. In this study, patients receiving mechanical ventilation in the intensive care unit will be randomly assigned to four groups using a simple randomization method:

  1. Control Group: Standard Eye Care

NCT07100990 — Treatment of Inflammatory Myelitis and Optic Neuritis With Early vs Rescue Plasma Exchange (TIMELY-PLEX)

StatusRecruiting
PhasePhase 3
SponsorMayo Clinic
Enrollment382
Study TypeINTERVENTIONAL
ConditionsOptic Neuritis; Myelitis; Myelitis, Transverse
Interventions;

The purpose of this research is to evaluate if early vs rescue Therapeutic Plasma Exchange (PLEX) treatment algorithm leads to better visual outcomes in severe Optic Neuritis and leads to better neurological disability outcomes in severe Transverse Myelitis.

NCT06658002 — Fungal Ulcer Treatment Augmented With Natamycin and Cyclosporine A

StatusRecruiting
PhasePhase 3
SponsorUniversity of California, San Francisco
Enrollment150
Study TypeINTERVENTIONAL
ConditionsFungal Keratitis; Corneal Ulcer
Interventions;

The goal of this clinical trial is to learn if adjunctive topical Cyclosporine A eye drops combined with standard of care topical Natamycin treatment improves vision outcomes in patients with fungal keratitis.

NCT07394257 — Intrastromal Moxifloxacin as an Adjunctive Therapy in Recalcitrant Bacterial Keratitis

StatusRecruiting
PhaseN/A
SponsorMinia University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBacterial Keratitis; Recalcitrant Infectious Keratitis; Corneal Ulcer
Interventions;

Bacterial keratitis is a potentially sight-threatening corneal infection that is commonly treated with intensive topical antibiotics. Despite appropriate therapy, some cases show inadequate clinical response, particularly when the infection involves the deep corneal stroma. Limited penetration of topical antibiotics into deeper corneal layers may contribute to treatment failure in these recalci…

NCT07329686 — Clinical Study of Intrastromal Anti-VEGF Injection for Corneal Neovascularization.

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsHerpes Simplex Keratitis; Corneal Neovascularization
Interventions;

Corneal stromal injection is an emerging local drug delivery method, characterized by strong targeting, high drug concentration, and prolonged duration of action. It has been preliminarily applied in the treatment of fungal keratitis and neurotrophic corneal diseases. This study aims to investigate the safety and efficacy of anti-VEGF drugs delivered via corneal stromal injection in neovascular…

NCT07322302 — RESTORE: Comparing Two Approaches to Repeat TT Surgery Performed by Integrated Eye Care Workers (IECWs)

StatusRecruiting
PhaseN/A
SponsorUniversity of North Carolina, Chapel Hill
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsTrachoma; Eye Diseases; Trichiasis
Interventions;

The primary objective of this randomized clinical trial is to determine whether repeat trichiasis surgery performed with Bevel-Rotate Advancement Procedure (B-RAP) improves surgical success compared to Bilamellar Tarsal Rotation (BLTR) among a group of 8-10 TT surgeons in Tanzania. The study aims to enroll 1,000 individuals with PTT. The primary outcome is repeat PTT within one year after surge…

NCT07377513 — Follow-up Compliance for Corneal Ulcer Patients With SMS Reminder

StatusRecruiting
PhaseN/A
SponsorSeva Canada Society
Enrollment310
Study TypeINTERVENTIONAL
ConditionsCorneal Ulcer
Interventions

Corneal ulcer is defined as the loss of corneal epithelium with underlying stromal infiltration and suppuration, accompanied by signs of inflammation, with or without hypopyon1. The condition may be caused by bacterial, fungal, viral or parasitic pathogens and carries a significant risk of corneal perforation and subsequent visual impairment2. These risks highlight the importance of timely trea…

NCT07537426 — The Efficacy of Intradermal Acupuncture for Ocular Surface Diseases After Intractable Facial Paralysis

StatusRecruiting
PhaseN/A
SponsorThe First Affiliated Hospital of Zhejiang Chinese Medical University
Enrollment78
Study TypeINTERVENTIONAL
ConditionsFacial Paralysis, Peripheral; Bell’s Palsy; Ocular Surface Disease
Interventions;

The purpose of this study is to explore the clinical efficacy of intradermal acupuncture in the treatment of ocular surface diseases after Intractable Facial Paralysis, and to seek effective and convenient treatment for ocular surface diseases after intractable peripheral facial paralysis. The main question it aims to answer is : Will the intradermal acupuncture intervention effectively reduce …

NCT07679412 — Evaluation of Safety and Efficacy of Autologous LB-DTK-CMV in Patients With Antiviral-Resistant and Refractory Cytomegalovirus Retinitis.

StatusRecruiting
PhaseN/A
SponsorLucasBio
Enrollment5
Study TypeINTERVENTIONAL
ConditionsCMV Retinitis
Interventions

The goal of this exploratory clinical study is to evaluate the safety and efficacy of Cytomegalovirus-Specific T cells (LB-DTK-CMV) to treat patients diagnosed with antiviral-resistant and refractory cytomegalovirus retinitis. The main questions it aims to answer are:

  • What adverse events occur after the infusion of LB-DTK-CMV?
  • What is the duration of efficacy following treatment?
  • Is ther…

NCT07565103 — Safety and Efficacy of SUM-191 for Patients With Bacterial Conjunctivitis

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorSenju USA, Inc.
Enrollment426
Study TypeINTERVENTIONAL
ConditionsBacterial Conjunctivitis
Interventions;

This is a seamless Phase I/II, randomized, double-masked, placebo-controlled, multicenter trial to evaluate single and multiple-dose safety and tolerability of SUM-191 in healthy participants in Parts 1 (SAD) and 2 (MAD) ; and multiple-dose efficacy and safety of SUM-191 in participants with bacterial conjunctivitis in Part 3.

Active, Not Recruiting

NCT01199562 — Infection Prophylaxis and Management in Treating Cytomegalovirus (CMV) Infection in Patients With Hematologic Malignancies Previously Treated With Donor Stem Cell Transplant

StatusActive, not recruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment153
Study TypeOBSERVATIONAL
ConditionsHematopoietic/Lymphoid Cancer; Accelerated Phase Chronic Myelogenous Leukemia; Acute Undifferentiated Leukemia; Adult Acute Lymphoblastic Leukemia in Remission; Adult Acute Myeloid Leukemia in Remission
Interventions; ;

RATIONALE: Infection prophylaxis and management may help prevent cytomegalovirus (CMV) infection caused by a stem cell transplant.

PURPOSE:This clinical trial studies infection prophylaxis and management in treating cytomegalovirus infection in patients with hematologic malignancies previously treated with donor stem cell transplant.

NCT01815749 — Genetically Modified T-cell Infusion Following Peripheral Blood Stem Cell Transplant in Treating Patients With Recurrent or High-Risk Non-Hodgkin Lymphoma

StatusActive, not recruiting
PhasePhase 1
SponsorCity of Hope Medical Center
Enrollment30
Study TypeINTERVENTIONAL
ConditionsAdult Grade III Lymphomatoid Granulomatosis; Cutaneous B-cell Non-Hodgkin Lymphoma; Extranodal Marginal Zone B-cell Lymphoma of Mucosa-associated Lymphoid Tissue; Intraocular Lymphoma; Nodal Marginal Zone B-cell Lymphoma
Interventions; ;

This phase I trial studies the side effects and best dose of genetically modified T-cells following peripheral blood stem cell transplant in treating patients with recurrent or high-risk non-Hodgkin lymphoma. Giving chemotherapy before a stem cell transplant helps stop the growth of cancer cells. When the healthy stem cells from a donor are infused into the patient they may help the patient’s b…

NCT07421440 — Flexible Bronchoscopy in Resistant Pneumonia in PICU

StatusActive, not recruiting
PhaseN/A
SponsorMansour Gomaa Mohammed Saleh
Enrollment58
Study TypeOBSERVATIONAL
ConditionsPneumonia; Resistant Pneumonia

Pneumonia is one of the most common and serious infections in children, especially those admitted to Pediatric Intensive Care Units (PICUs). Some children do not improve after at least five days of appropriate broad-spectrum antibiotic treatment. This condition is known as resistant or non-resolving pneumonia.

Flexible fiberoptic bronchoscopy (FFB) is a procedure that allows doctors to directl…

NCT05879419 — Recombinant Herpes Zoster Vaccine in Patients With Autoimmune Rheumatic Diseases

StatusActive, not recruiting
PhasePhase 4
SponsorUniversity of Sao Paulo General Hospital
Enrollment2005
Study TypeINTERVENTIONAL
ConditionsRheumatoid Arthritis; Spondylitis, Ankylosing; Spondyloarthritis; Systemic Lupus Erythematosus; Sjogren’s Syndrome
Interventions; ;

Introduction: Patients with autoimmune rheumatic diseases (ARDs), rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis (PAs), ankylosing spondylitis (AS), systemic lupus erythematosus (SLE), primary Sjögren’s syndrome (pSS) , systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM) and primary vasculitides, have a high risk of herpes zoster (HZ) infectio…

Not Yet Recruiting

NCT07323615 — A Comparative Study of the Efficacy and Safety of Two Methods in the Treatment of Skin Wounds

StatusNot yet recruiting
PhaseN/A
SponsorShanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Enrollment98
Study TypeINTERVENTIONAL
ConditionsWound Debridement
Interventions

This study will compare the experimental group (debridement assisted by surgical microscope + VSD) and the control group (debridement under naked-eye observation + VSD) in terms of the rate of change in BWAT scores at one week postoperatively when the VSD is removed, daily wound negative-pressure drainage volume and pain scores within the first postoperative week, and results of two wound bacte…

NCT07418333 — Efficacy of EPD-09-25 for Eyelid Hygiene Before and After Eye Surgery.

StatusNot yet recruiting
PhaseN/A
SponsorVISUfarma SpA
Enrollment100
Study TypeINTERVENTIONAL
ConditionsCataract Surgery; Ocular Infections
Interventions

This is an interventional, open-label, two-arms clinical trial, randomized 1:1 (EPD treatment or no eyelid hygiene treatment) in patients scheduled for eye surgery (cataract surgery). The purpose of the study is to evaluate the importance of the cleansing action of EPD-09-25 before and after eye surgery.

NCT07657143 — Evaluation of the Impact of Oral Ivermectin on Musca Sorbens Flies, Putative Vector of Trachoma

StatusNot yet recruiting
PhasePhase 4
SponsorLondon School of Hygiene and Tropical Medicine
Enrollment12
Study TypeINTERVENTIONAL
ConditionsSurvival of Flies Developing in Faecal Samples
Interventions

Trachoma is caused by repeated Chlamydia trachomatis infection in the eye. Routes of infection include close person-to-person contact and contaminated clothing. In addition, the bazaar fly Musca sorbens has been implicated in transmission. These flies frequently visit the faces of children and have been found positive for C. trachomatis, which may be transferred from the body of the flies or th…

NCT07513623 — Systemic and Topical Antiviral Control of Cytomegalovirus Anterior Uveitis: Treatment Outcomes - Trials I and II

StatusNot yet recruiting
PhasePhase 2
SponsorUniversity of California, San Francisco
Enrollment117
Study TypeINTERVENTIONAL
ConditionsCytomegalovirus (CMV); Anterior Uveitis; Infectious Uveitis; CMV Infection
Interventions; ;

The goal of this clinical trial is to compare antiviral treatment strategies for cytomegalovirus (CMV) anterior uveitis - a viral infection causing inflammation inside the front of the eye - in immunocompetent adults aged 18 years and older. The main questions it aims to answer are:

Does oral valganciclovir reduce aqueous humor CMV viral load more effectively than topical ganciclovir 2% eye dr…

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…

NCT07308938 — Fluorometholone Study

StatusNot yet recruiting
PhasePhase 2
SponsorVishal Jhanji
Enrollment174
Study TypeINTERVENTIONAL
ConditionsKeratitis Bacterial; Corneal Ulcer (Diagnosis)
Interventions;

The investigators seek to determine whether adjunctive topical fluorometholone (FML) improves best-corrected visual acuity (BCVA) at 3 months in patients with bacterial corneal ulcers compared with standard topical antibiotic therapy alone.

Completed Trials

NCT00664313 — TBTC Study 30: Safety and Tolerability of Low Dose Linezolid in MDR TB

StatusCompleted
PhasePhase 1 / Phase 2
SponsorCenters for Disease Control and Prevention
Enrollment36
Study TypeINTERVENTIONAL
ConditionsMulti-drug Resistant Tuberculosis; Extensively Drug Resistant Tuberculosis
Interventions;

This study evaluated the safety and tolerability of low-dose linezolid (600 mg once daily) administered for 16 weeks as part of an optimized background regimen for the treatment of multidrug-resistant tuberculosis (MDR-TB).

NCT01208792 — Auto-immunity and Pulmonary Arterial Hypertension

StatusCompleted
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment629
Study TypeINTERVENTIONAL
ConditionsPulmonary Arterial Hypertension; HIV Infection; Congenital Heart Defect; Systemic Sclerosis; Connective Tissue Disease
Interventions;

The investigators have recently evidenced the presence of antibodies to endothelial cells and fibroblasts in patients with idiopathic or SSc-associated PAH. The investigators also have identified several target antigens of anti-fibroblasts antibodies.

The objective of this study is to further investigate for the presence of antibodies to endothelial cells and fibroblasts in patients and charac…

NCT01820910 — Phase II Trial of First-line Doxycycline for Ocular Adnexal Marginal Zone Lymphoma Treatment

StatusCompleted
PhasePhase 2
SponsorInternational Extranodal Lymphoma Study Group (IELSG)
Enrollment44
Study TypeINTERVENTIONAL
ConditionsMarginal Zone Lymphoma of Ocular Adnexal
Interventions

Objective of this trial is to establish the efficacy of an upfront targeted therapy consisting of Chlamydophila psittaci (Cp)-eradicating therapy with prolonged administration of doxycycline followed by eradication monitoring and antibiotic re-treatment at infection re-occurrence in patients with newly diagnosed ocular adnexae marginal zone lymphoma The primary endpoint is the 2-year progressio…

NCT02754583 — Sanitation, Water, and Instruction in Face-washing for Trachoma I/II

StatusCompleted
PhasePhase 3
SponsorUniversity of California, San Francisco
Enrollment47605
Study TypeINTERVENTIONAL
ConditionsTrachoma
Interventions; ;

SWIFT I is a series of 3 cluster-randomized trials designed to assess several alternative strategies for trachoma control in communities that have been treated with many years of mass azithromycin distributions. The first trial (named WUHA) compares communities that receive a comprehensive Water, Sanitation, and Hygiene (WASH) package to those that receive no intervention. The second trial (nam…

NCT03484507 — Parasitic Ulcer Treatment Trial Pilot

StatusCompleted
PhasePhase 2
SponsorUniversity of California, San Francisco
Enrollment49
Study TypeINTERVENTIONAL
ConditionsAcanthamoeba Keratitis
Interventions; ;

This is a study of optimal treatments for acanthamoeba keratitis. In the first part of the study, participants will be randomized to chlorhexidine monotherapy or chlorhexidine plus povidone iodine. After four weeks of therapy, participants will be re-randomized to early corticosteroids, later corticosteroids, or placebo.

NCT03848858 — Efficacy of EMDR Therapy, as Compared to Treatment as Usual, in Reducing Clinical Symptoms in People With HIV

StatusCompleted
PhaseN/A
SponsorParc de Salut Mar
Enrollment40
Study TypeINTERVENTIONAL
ConditionsHIV/AIDS; Psychological Trauma; PTSD
Interventions

People living with HIV may suffer HIV-related psychological trauma. Studies also show that this group is vulnerable to non-HIV-related trauma. Trauma can increase vulnerability to stress and reducing the ability to cope. It can have a negative impact on treatment adherence, treatment outcomes, functioning and health-related quality of life. However, despite evidence showing psychological trauma…

NCT07407972 — Effect of Optıc Nerve Dıameter ın Tymphanoplasty Surgery Performed ın Lateral Head Posıtıon

StatusCompleted
PhaseN/A
SponsorBursa Yuksek Ihtisas Training and Research Hospital
Enrollment53
Study TypeINTERVENTIONAL
ConditionsOptic Nerve Diameter; Intracranial Pressure Increase
Interventions

Studies exist to determine the effect of laparoscopic surgical procedures on increased intra-abdominal pressure; these studies include optic nerve sheath diameter (ONSD) measurement in various positions such as trendelenburg and prone, and the effect of the laryngoscope used in intubation on increased intracranial pressure. In these situations, changes in cerebral blood flow and intracranial pr…

NCT04185402 — Azithromycin Reduction to Reach Elimination of Trachoma

StatusCompleted
PhasePhase 4
SponsorUniversity of California, San Francisco
Enrollment3931
Study TypeINTERVENTIONAL
ConditionsTrachoma
Interventions

The investigators propose a randomized controlled trial of discontinuation versus continuation of annual mass azithromycin distribution in hypoendemic communities of Maradi, Niger. The investigators will randomize communities with up to 20% Trachomatous Inflammation - Follicular (TF) prevalence following at least 5 years of mass azithromycin distribution to discontinuation or continuation of 3 …

NCT05286203 — Ocular Pathogen and Transcriptome Investigation Using Comprehensive Sequencing

StatusCompleted
PhaseN/A
SponsorUniversity of California, San Francisco
Enrollment100
Study TypeINTERVENTIONAL
ConditionsUveitis; Infectious Disease
Interventions;

This is a multi-center randomized controlled evaluator-masked trial designed to compare metagenomic deep sequencing (MDS) versus standard of care testing for improvement of outcomes for intraocular infections. Patients with presumed intraocular infections who meet the eligibility criteria will be randomized to receive MDS testing results or not to receive MDS testing results. All patients will …

NCT05110001 — Rose Bengal Electromagnetic Activation With Green Light for Infection Reduction

StatusCompleted
PhasePhase 3
SponsorUniversity of California, San Francisco
Enrollment330
Study TypeINTERVENTIONAL
ConditionsAcanthamoeba Keratitis; Fungal Keratitis
Interventions; ;

Rose Bengal Electromagnetic Activation with Green light for Infection Reduction (REAGIR ) is an international, randomized, doubled masked, clinical trial. The purpose of this study is to determine differences in 6-month visual acuity between medical antimicrobial treatments alone versus antimicrobial treatment plus cross-linking with rose Bengal (RB-PDT).

Patients presenting to one of the Arav…

NCT05774496 — Pregnancy and Congenital Toxoplasmosis

StatusCompleted
PhaseN/A
SponsorHospices Civils de Lyon
Enrollment76
Study TypeOBSERVATIONAL
ConditionsCongenital Toxoplasmosis; Retinochoroiditis
Interventions

The Toxoplasma gondii parasite causes toxoplasmosis. It is characterized by persistent cysts mostly localised in the brain and ocular areas. In the case of immunodeficiency, those cysts are likely to reactivate. During pregnancy, an infection exposes the foetus to a variety of consequences, from severe neurologic lesions to subclinical forms at birth. However, those forms are likely to complica…

NCT06437223 — Study of Xiflam™ Treatment in Patients Post COVID-19 Infection Suffering From What is Known as Long COVID (LC)

StatusCompleted
PhasePhase 2
SponsorInflammx Therapeutics Inc
Enrollment16
Study TypeINTERVENTIONAL
ConditionsLong COVID
Interventions;

The primary objective of this study is to evaluate the safety and efficacy of Xiflam versus Placebo in patients who present with signs and symptoms of Long COVID.

Xiflam (n=10) or placebo (n=5) will be administered orally once a day (QD) for 12 weeks.

NCT06579885 — Ocular Complications of Mpox in the Democratic Republic Congo

StatusCompleted
PhaseN/A
SponsorInstitute of Tropical Medicine, Belgium
Enrollment320
Study TypeOBSERVATIONAL
ConditionsMonkeypox; Mpox (Monkeypox)

This is an observational study in which patients diagnosed with mpox will be enrolled, will undergo standard ophthalmological examinations of their eyes to see if there are any complications of mpox. The study will primarily assess the presence of ophthalmological signs and symptoms at enrollment.

NCT07514845 — First-line Surgical Versus Medical Treatment: A Retrospective Study From 2014 to 2024 in Brest (BRESTE)

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Brest
Enrollment170
Study TypeOBSERVATIONAL
ConditionsEndophthalmitis
Interventions

The goal of this observational cohort study is to evaluate the impact of early pars plana vitrectomy (PPV) on visual outcomes in adults diagnosed with acute endophthalmitis. It also aims to identify prognostic factors associated with visual recovery.

The main questions it aims to answer are:

Does early PPV (within 48 hours of diagnosis) improve visual acuity at 1 month compared with initial m…

NCT07195864 — Retrospective Chart Review of Patients With Acanthamoeba Keratitis Who Have Received 0.8 mg/mL Polihexanide as Part of the “Medicines in Special Situations” (Medicamentos en Situaciones Especiales) Program in Spain.

StatusCompleted
PhaseN/A
SponsorSIFI SpA
Enrollment23
Study TypeOBSERVATIONAL
ConditionsAcanthamoeba Keratitis
Interventions

The study will be a multicentric, retrospective, non-interventional medical chart review of patients with AK who initiated a treatment with 0.8 mg/ml polihexanide as part of the Spanish Medicines in Special Situations program, whether they fully completed the treatment or not.

Baseline date is defined as the date of 0.8 mg/ml polihexanide initiation. The Study Period for each patient will be c…

Other (Terminated)

NCT07396831 — Necessity of Post-operative Eye Drops

StatusTerminated
PhaseN/A
SponsorLoma Linda University
Enrollment48
Study TypeOBSERVATIONAL
ConditionsPars Plana Vitrectomy; Scleral Buckling; Surgical Outcomes; Infection Prophylaxis

The goal of this clinical study is to determine if antibiotic eye drops are needed after retinal surgery to prevent infection. Currently, patients are prescribed antibiotic eye drops to use for several weeks after they undergo retina surgery. The main question that we are trying to answer is:

- Are postoperative eye drops necessary to prevent eye infections after retina surgery? Patients will…

Other (Withdrawn)

NCT06289647 — Azithromycin Reduction to Reach Elimination of Trachoma B

StatusWithdrawn
PhasePhase 4
SponsorUniversity of California, San Francisco
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsTrachoma
Interventions

The investigators propose a randomized controlled trial of discontinuation versus continuation of annual mass azithromycin distribution in hypoendemic communities of Maniema, DRC. The investigators will randomize communities with up to 20% Trachomatous Inflammation - Follicular (TF) prevalence following at least 5 years of mass azithromycin distribution to discontinuation or continuation of 3 a…

NCT04230811 — Diagnosing Corneal Infection

StatusWithdrawn
PhaseN/A
SponsorUniversity of Edinburgh
EnrollmentN/A
Study TypeOBSERVATIONAL
ConditionsCorneal Ulcer (Diagnosis)
Interventions

Microbial keratitis is a common and serious eye disease in Edinburgh. Prompt treatment with antibiotics can prevent sight loss, and identification of the micro-organism and its antibiotic sensitivities are key to appropriate management. Standard practice of collecting infected material from the cornea using a blade can be distressing and time-consuming. Corneal impression membranes (CIM) have r…