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Completed

NCT Number: NCT00296621

Effect of Oral Glutamine on Muscle Mass and Function in Duchenne Muscular Dystrophy

The purpose of this study is to determine whether long-term oral glutamine supplementation is effective in improving muscle mass and function in children with Duchenne muscular dystrophy (DMD).

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Key information

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

Centre d'Investigation Clinique, Hôpital Cardiologique, CHR&U de Lille, Lille, France

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About this study

Glutamine inhibits whole body protein degradation in children with Duchenne Muscular Dystrophy (DMD). The effect is observed after 5 h oral glutamine administration and is also found when glutamine is given over a 10-day period. This multi-site national study aims to evaluate the functional benefit of long-term oral glutamine administration in 30 DMD children using a randomized double-blind placebo-controlled cross-over design. The study includes two 4-month periods: 1) a treatment period in which the subject receives oral glutamine (0.5 g/kg/d) and 2) a control period in which the subject receives a placebo. The order of treatment allocation is randomized. The two 4-month periods are separated by a 1 month wash-out period. The children are monitored every 2 months during period 1 (M0, M2, M4) and period 2 (M5, M7, M9) in the clinical investigation centres of Hospital Robert Debré in Paris and the CHR&U de Lille, as well as the clinical research centre of the CHU de Poitiers. Evidence of a functional benefit would involve evaluating the administration of glutamine over longer periods (as early as possible following diagnosis) among severely handicapped children and in other chronic pathologies associated with increased muscle protein catabolism. In DMD, such evidence would enable children to undergo gene therapy under improved physical condition.

Comparisons: Glutamine administration compared to placebo on the following outcome measures: walking speed on a standard course, work (kcal) and power (kcal/s) in relation to effort, body composition (bioelectrical impedance analysis and BIPHOTONIC absorptiometry), muscle mass (24-h urinary creatinine excretion), indices of protein degradation (CPK and 3-methyl histidine excretion) and biochemical parameters (electrolytes, fasting glucose, transaminases, insulin, IgfI, Igf-BPI).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of Duchenne muscular dystrophy
  • Able to walk >170 m
  • Absence of hepatic insufficiency
  • Absence of renal insufficiency

Exclusion criteria

  • Dependent upon wheelchair
  • Body weight >60kg
  • Liver failure
  • Kidney failure
  • Surgery scheduled during the year following the first visit

Treatment and study plan

L-glutamine

Drug

L-Glutamine

Placebo

Drug

placebo

Primary outcomes

  1. walking speed at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

Secondary outcomes

  1. work (kcal) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  2. power (kcal/s) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  3. 2-minute walk test at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  4. body composition (bioelectrical impedance analysis) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  5. body composition (BIPHOTONIC absorptiometry) at 4,9 months

    Time frame: at 4,9 months

  6. muscle mass (24-h urinary creatinine excretion) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  7. indices of protein degradation (CPK and 3-methyl histidine excretion) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

  8. biochemical parameters (electrolytes, fasting glucose, transaminases, insulin, IgfI, Igf-BP3) at 0,2,4,5,7,9 months

    Time frame: at 0,2,4,5,7,9 months

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Efficacy Study of Oral Glutamine Supplementation in Duchenne Muscular Dystrophy

Acronym: MDB-GLN

Important dates

Study start
2006
Primary completion
2008
Study completion
2007
First posted
Feb 27, 2006
Registry last updated
Dec 21, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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