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Completed Phase 4 Interventional Results available

Multicenter Uveitis Steroid Treatment (MUST) Trial

ClinicalTrials.gov ID: NCT00132691

Public ClinicalTrials.gov record NCT00132691. 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 Oct 26, 2026, 6:22 AM EDT

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

Brief summary

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

The purpose of this study is to compare the effectiveness of standardized systemic therapy versus fluocinolone acetonide implant therapy for the treatment of severe cases of non-infectious intermediate uveitis, posterior uveitis, or panuveitis.

Study identification

NCT ID
NCT00132691
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
255 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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
Sep 2005 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
Nov 25, 2016

2005 – 2010

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Jacobs Retina Center, UCSD La Jolla California 92037 —
Doheny Eye Institute, USC Los Angeles California 90033 —
Jules Stein Eye Institute, UCLA Los Angeles California 90095 —
Proctor Foundation, UCSF San Francisco California 94143 —
Anne Bates Leach Eye Hospital, University of Miami Miller School of Medicine Miami Florida 33136 —
University of South Florida Tampa Florida 33612 —
Emory University Atlanta Georgia 30322 —
Rush University Medical Center Chicago Illinois 60612 —
University of Illinois at Chicago Eye Center Chicago Illinois 60612 —
Wilmer Eye Institute, Johns Hopkins University Baltimore Maryland 21287 —
National Eye Institute, NIH Bethesda Maryland 20892 —
Massachusetts Eye Research & Surgery Institute Cambridge Massachusetts 02142 —
Kellogg Eye Center, University of Michigan Ann Arbor Michigan 48105 —
Barnes Retina Institute St Louis Missouri 63110 —
New York Eye and Ear Infirmary New York New York 10016 —
Duke Eye Center, Duke University Durham North Carolina 27710 —
Scheie Eye Institute, University of Pennsylvania Philadelphia Pennsylvania 19104 —
Texas Retina Associates Dallas Texas 75231 —
Vitreoretinal Consultants Houston Texas 77030 —
John A. Moran Eye Center, University of Utah Salt Lake City Utah 84132 —
Virginia Eye Consultants Norfolk Virginia 23502 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00132691, 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 Nov 25, 2016 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00132691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →