Sponsor:
Helen Keller Eye Research Foundation
Code:
NCT07146516
Conditions
Stickler Syndrome Type 1
Stickler Syndrome Type 2
Eligibility Criteria
Sex: All
Age: 0+
Healthy Volunteers: Not accepted
Interventions
Prophylactic (non-invasive) Laser Retinopexy
Brief summary:
Conditions
Stickler Syndrome Type 1
Stickler Syndrome Type 2
Study ID
NCT07146516
Start date
Oct 30, 2025
Status verified date
Jun, 2026
Completion date
Dec, 2035
Anticipated
Primary completion date
Dec, 2035
Anticipated
Eligibility Criteria
Sex: All
Age: 0+
Healthy Volunteers: Not accepted
Enrollment
500 participants
Anticipated
Intervention Model
Single group
Primary purpose
Prevention
Arms
experimental: Children, Adolescents, and Adults with SS treated with Prophylactic Laser Retinopexy
Interventions
Prophylactic (non-invasive) Laser Retinopexy
Primary outcome measure
Central contacts
Five Lakes Clinical Research Consultants, LLC
contactus@fivelakesconsultants.comLocations
Retina Specialists of Alabama
Recruiting
Birmingham, Alabama, United States, 35233
Contacts
Principal Investigator:
Mathew Sapp, MD
Associated Retinal Consultants, P.C.
Recruiting
Royal Oak, Michigan, United States, 48073
Contacts
Principal Investigator:
Matthew Trese, D.O.
Retina Consultants of Minnesota
Recruiting
Minneapolis, Minnesota, United States, 55435
Contacts
Principal Investigator:
Peter J Belin, MD
Mayo Clinic
Recruiting
Rochester, Minnesota, United States, 55905
Contacts
Tennessee Retina, P.C.
Recruiting
Nashville, Tennessee, United States, 37203
Contacts
Principal Investigator:
Franco Recchia, MD
Sponsor
Helen Keller Eye Research Foundation
Last update posted
Jul 1, 2026
Last verified
Jun, 2026
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Helen Keller Eye Research Foundation on 2026-07-01.