Patient Guide: A Study Conducted to Evaluate the Conjunctiva and Tenon's Capsule Status of Healthy Subjects and in Participants With Neovascular Age-related Macular Degeneration (nAMD)/Diabetic Macular Edema (DME)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 19 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06723288
Status: 🟢 Enrolling Now
Condition: Neovascular Age-related Macular Degeneration, Diabetic Macular Edema
Phase: Not Specified

Where You Can Participate

This study is available at 19 locations across the country.

Top locations include:
  • • Oviedo, Asturias
  • • L?hospitalet De Llobregat, Barcelona
  • • San Cugat Del Valles, Barcelona
  • • And 16 more locations

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A Study Conducted to Evaluate the Conjunctiva and Tenon's Capsule Status of Healthy Subjects and in Participants With Neovascular Age-related Macular Degeneration (nAMD)/Diabetic Macular Edema (DME) - Join Clinical Trial NCTNCT06723288

How to Join This Clinical Trial - NCTNCT06723288

Learn how to participate in this Not Specified trial studying an investigational therapy for Neovascular Age-related Macular Degeneration, Diabetic Macular Edema. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Neovascular Age-related Macular Degeneration, Diabetic Macular Edema. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Neovascular Age-related Macular Degeneration, Diabetic Macular Edema
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06723288 - 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 19 locations. Find a study site near you:

Clinical Research Site

Oviedo, Asturias 33012 - Spain

Status: RECRUITING

Clinical Research Site

L?hospitalet De Llobregat, Barcelona 08907 - Spain

Status: RECRUITING

Clinical Research Site

San Cugat Del Valles, Barcelona 08195 - Spain

Status: RECRUITING

Clinical Research Site

Majadahonda, Madrid 28222 - Spain

Status: RECRUITING

Clinical Research Site

Pamplona, Navarra 31008 - Spain

Status: RECRUITING

Clinical Research Site

Burjassot, Valencia 46100 - Spain

Status: RECRUITING

Clinical Research Site

Barcelona, 08021 - Spain

Status: RECRUITING

Clinical Research Site

Barcelona, 08022 - Spain

Status: RECRUITING

Clinical Research Site

Barcelona, 08035 - Spain

Status: RECRUITING

Clinical Research Site

Barcelona, 08036 - Spain

Status: RECRUITING

And 9 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Neovascular Age-related Macular Degeneration, Diabetic Macular Edema:

  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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