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Completed Phase 3 Interventional Results available

Finding the Optimum Regimen for Duchenne Muscular Dystrophy

ClinicalTrials.gov ID: NCT01603407

Public ClinicalTrials.gov record NCT01603407. 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 7, 2026, 11:55 AM EDT

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

Official title

Duchenne Muscular Dystrophy: Double-blind Randomized Trial to Find Optimum Steroid Regimen

Brief summary

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

The Finding the Optimum Regimen for Duchenne Muscular Dystrophy (FOR DMD) study will compare three ways of giving corticosteroids to boys with Duchenne muscular dystrophy (DMD) to determine which of the three ways increases muscle strength the most, and which causes the fewest side effects. Using the results of this study, the investigators aim to provide patients and families with clearer information about the best way to take these drugs.

Study identification

NCT ID
NCT01603407
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
University of Rochester
Other
Enrollment
196 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
4 Years to 7 Years
Sex
Male
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
Jan 2013 (Type not available)
Primary completion
Nov 2019 (Actual)
Completion
Nov 2019 (Actual)
Last update posted
Aug 12, 2022

2013 – 2019

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
University of California Los Angeles (UCLA) Medical Center Los Angeles California 90095 —
University of California Davis Medical Center Sacramento California 95817 —
Children's National Medical Center Washington D.C. District of Columbia 20010 —
Nemours Children's Hospital Orlando Florida 32827 —
Ann and Robert H. Lurie Children's Hospital of Chicago Chicago Illinois 60614 —
University of Kansas Medical Center Kansas City Kansas 66160 —
Boston Children's Hospital Boston Massachusetts 02115 —
University of New Mexico Health Science Center Albuquerque New Mexico 87131 —
University of Rochester Medical Center Rochester New York 14642 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 —
Nationwide Children's Hospital Columbus Ohio 43205 —
Penn State Hershey Medical Center Hershey Pennsylvania 17033 —
Vanderbilt Children's Hospital Nashville Tennessee 37232 —
University of Utah Medical Center Salt Lake City Utah 84132 —

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01603407, 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 Aug 12, 2022 · Synced Oct 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01603407 live on ClinicalTrials.gov.

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