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Completed No phase listed Observational

Generation of Induced Pluripotent Stem (iPS) Cell Lines From Skin Fibroblast Cells of Participants With Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT03372746

Public ClinicalTrials.gov record NCT03372746. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 1:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Generation of Induced Pluripotent Stem (iPS) Cell Lines From Skin Fibroblast Cells of Participants With Age-Related Macular Degeneration: An Ancillary Study to the Age-Related Eye Disease Study-2 (AREDS2)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Background: Age-related macular degeneration (AMD) is the leading cause of blindness in the United States. Currently, there is no safe way to obtain cells from the eye to study. But researchers now can turn other types of cells, like skin or blood, into induced pluripotent stem (iPS) cells. These can be grown in a lab and turned into other types of cells, like cells from the eye. This will allow researchers to understand and treat diseases of the eye such as AMD. Objectives: To establish a bank of samples that can be changed into other cell types, such as eye cells, to better understand diseases such as AMD. Also to test drugs in order to treat various eye diseases. Eligibility: People who provided DNA samples in another protocol (07-EI-0025) Design: Participants will be screened with their data from the previous protocol. Participants with select genetic variants will be chosen and contacted via phone. Participants will have a punch skin biopsy. The skin will be washed. A numbing medication will be injected. A small piece of skin will be removed with a biopsy tool. The site will be covered with a dressing. They will receive instructions on how to care for the area. They will have follow-up visits if needed for clinical care for the area. Participants may be asked to return if their first sample did not provide enough cells for the lab. Participants sample will be developed into eye cells. The cells will be used to understand diseases and test new drugs.

Study identification

NCT ID
NCT03372746
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
187 participants

Conditions and interventions

Conditions

Interventions

Not listed

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 22, 2018
Primary completion
Mar 20, 2019
Completion
Mar 20, 2019
Last update posted
Apr 4, 2019

2018 – 2019

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Retina-Vitreous Associates Med Group Beverly Hills California 90211
Bascom Palmer Eye Institute Miami Florida 33136
Emory University Eye Center Atlanta Georgia 30322
Retina Vitreous Associates of Kentucky Lexington Kentucky 40509
National Institutes of Health Clinical Center Bethesda Maryland 20892
Elman Retina Group, P.A. Rosedale Maryland 21237
Massachusetts Eye and Ear Infirmary Boston Massachusetts 02114-3096
Vision Research ROPARD Foundation/Associated Retinal Consultants, Grand Rapids Grand Rapids Michigan 49546
Vision Research ROPARD Foundation/Associated Retinal Consultants, Novi Novi Michigan 48375
Charlotte Eye Ear Nose & Throat Associates Charlotte North Carolina 28210
Casey Eye Institute Portland Oregon 97210
Texas Retina Associates Dallas Texas 75231
John Moran Eye Center, University of Utah Salt Lake City Utah 84132
University of Wisconsin-Madison Madison Wisconsin 53705

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03372746, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2019 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03372746 live on ClinicalTrials.gov.

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