Patient Guide: Observational Study to Investigate the Short-term Effects of Transcorneal Electrical Stimulation on Visual Performance

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  • ✓ Connect directly with study coordinators at 1 participating sites
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Trial ID: NCTNCT07548944
Status: 🟢 Enrolling Now
Condition: Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy
Phase: Not Specified

Find a Study Location Near You

This study is available at 1 research site. We'll help you connect with the location that's right for you.

Participating sites include:
  • • Frankfurt am Main,

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Observational Study to Investigate the Short-term Effects of Transcorneal Electrical Stimulation on Visual Performance - Join Clinical Trial NCTNCT07548944

How to Join This Clinical Trial - NCTNCT07548944

Learn how to participate in this Not Specified trial studying Transcorneal Electrical Stimulation using the OkuStim System for Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy
Treatment Being Tested
Transcorneal Electrical Stimulation using the OkuStim System
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT07548944 - 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 1 locations. Find a study site near you:

Clinical Research Site

Frankfurt am Main, 60549 - Germany

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy:

  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

Why Choose Quri.ai as Your Clinical Trial Matching Service

Quri.ai is a free clinical trial matching service that helps patients connect with research sites. We make it easier to:

  • Find clinical trials that match your condition
  • Get matched to the right study location near you
  • Connect directly with study coordinators
  • Understand if you qualify with simplified eligibility screening
  • Navigate the enrollment process with personalized support
  • Access new treatments through clinical research participation