CompletedNCT02575430
Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT
Studying OBSOLETE: Inherited retinal disorder
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- QLT Inc.
- Principal Investigator
- David Saperstein, MDQLT Inc.
- Intervention
- No treatment: retrospective chart review(other)
- Enrollment
- 59 enrolled
- Eligibility
- 8 years · All sexes
- Timeline
- 2015 – 2016
Study locations (9)
- Wilmer Eye Institute - Johns Hopkins Hospital, Baltimore, Maryland, United States
- Casey Eye Institute - Marquam Hill, Portland, Oregon, United States
- The Hospital for Sick Children, Ophthalmology and Vision Sciences, Toronto, Ontario, Canada
- Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada
- Glostrup Hospital and National Eye Clinic at the Kennedy Center, Glostrup Municipality, Copenhagen, Denmark
- STZ Eyetrial at the Department of Ophthalmology - University of Tübingen, Tübingen, Germany
- Rotterdam Ophthalmic Institute, Rotterdam, Netherlands
- Jules Gonin Eye Hospital - Oculogenetic Unit, Lausanne, Switzerland
- Moorfields Eye Hospital - Research and Treatment Centre, London, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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