UNITY VCS Vitreoretinal Surgery - Join Clinical Trial NCTNCT07054281
How to Join This Clinical Trial - NCTNCT07054281
Learn how to participate in this NA trial studying an investigational therapy for Epiretinal Membrane, Macular Hole, Visually Significant Vitreous Floater, Vitreomacular Traction, Vitreous Hemorrhage, Proliferative Diabetic Retinopathy, Rhegmatogenous Retinal Detachment, Retained Lens Material in the Posterior Segment. Current status: NOT_YET_RECRUITING.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Epiretinal Membrane, Macular Hole, Visually Significant Vitreous Floater, Vitreomacular Traction, Vitreous Hemorrhage, Proliferative Diabetic Retinopathy, Rhegmatogenous Retinal Detachment, Retained Lens Material in the Posterior Segment. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Epiretinal Membrane, Macular Hole, Visually Significant Vitreous Floater, Vitreomacular Traction, Vitreous Hemorrhage, Proliferative Diabetic Retinopathy, Rhegmatogenous Retinal Detachment, Retained Lens Material in the Posterior Segment
- Treatment Being Tested
- Investigational treatment
- Study Phase
- NA - Research study
- Enrollment Status
- NOT_YET_RECRUITING
- Study Identifier
- NCTNCT07054281 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 8 locations. Find a study site near you:
Clinical Research Site
Scottsdale, Arizona 85255 - United States
Status: Contact for availability
Clinical Research Site
Laguna Hills, California 92653 - United States
Status: Contact for availability
Clinical Research Site
West Des Moines, Iowa 50266 - United States
Status: Contact for availability
Clinical Research Site
Albuquerque, New Mexico 87109 - United States
Status: Contact for availability
Clinical Research Site
New York, New York 10003 - United States
Status: Contact for availability
Clinical Research Site
Rapid City, South Dakota 57701 - United States
Status: Contact for availability
Clinical Research Site
Germantown, Tennessee 38138 - United States
Status: Contact for availability
Clinical Research Site
Salt Lake City, Utah 84107 - United States
Status: Contact for availability
How to Enroll in This Study
To learn more about participating in this NA clinical trial for Epiretinal Membrane, Macular Hole, Visually Significant Vitreous Floater, Vitreomacular Traction, Vitreous Hemorrhage, Proliferative Diabetic Retinopathy, Rhegmatogenous Retinal Detachment, Retained Lens Material in the Posterior Segment:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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