Clinical Trials Directory

Trials / Completed

CompletedNCT00000116

Randomized Trial of DHA for Retinitis Pigmentosa Patients Receiving Vitamin A

Clinical Trial of Docosahexaenoic Acid (DHA) in Patients With Retinitis Pigmentosa Receiving Vitamin A Treatment

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
221 (actual)
Sponsor
Carol Weigel DiFranco · NIH
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The purpose of this trial is to determine whether a nutritional supplement in addition to vitamin A will slow the course of retinitis pigmentosa.

Detailed description

Retinitis pigmentosa (RP) is a group of inherited retinal degenerations with a worldwide prevalence of approximately 1 in 4,000. Patients typically report night blindness and difficulty with midperipheral visual field in adolescence. As the condition progresses, they lose far peripheral visual field. Most patients have reductions in central vision by age 50 to 80 years. Based on electroretinograms (ERGs), the course of the disease can be slowed on average among adults on 15,000 IU/day of vitamin A palmitate. While conducting the trial on the effects of vitamin A on RP, it became apparent that another substance in the diet could be affecting the course of the disease. This prompted the present randomized, controlled trial. This study is a randomized, controlled, double-masked trial with a planned duration of 5 years. Patients with the common forms of RP are assigned to either a test or a control group. All receive 15,000 IU/day of vitamin A palmitate in addition to either 1200 mg/d of docosahexaenoic acid or control capsules. Participants will not know the contents of the supplement or the group to which they have been assigned until the end of the trial. The main outcome measurement is the total point score on the Humphrey Field Analyzer (HFA). In addition, computer-averaged 30-Hz cone ERG amplitudes and visual acuity are measured annually.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTVitamin A15000 IU/d as retinyl palmitate
DIETARY_SUPPLEMENTDocosahexaenoic acid1200 mg/d
DIETARY_SUPPLEMENTControl fatty acid

Timeline

Start date
1996-05-01
Primary completion
2002-09-01
Completion
2002-09-01
First posted
1999-09-24
Last updated
2023-03-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00000116. Inclusion in this directory is not an endorsement.