Patient Guide: UNITY VCS Vitreoretinal Surgery

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 8 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07054281
Status: NOT_YET_RECRUITING
Condition: 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
Phase: NA

Where You Can Participate

This study is available at 8 locations across the country.

Top locations include:
  • • Scottsdale, Arizona
  • • Laguna Hills, California
  • • West Des Moines, Iowa
  • • And 5 more locations

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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:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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