The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis
NCT02267005 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 13
Last updated 2018-05-11
Summary
This project will bring together a multidisciplinary team of pediatric rheumatologists, neurologists, metabolic geneticists and exercise physiologists to determine the effect of creatine (CR) supplementation on muscle function and muscle metabolism in children with Dermatomyositis (DM). The investigators propose using well-established exercise testing techniques as well as new, powerful exercise imaging protocols in order to better delineate the effects of CR on muscle pathophysiology in a non-invasive way. Evidence from this study will provide information regarding the effect of creatine supplementation on muscle function in DM. Improvements in muscle function and fatigue through CR use may also contribute to an improvement in quality of life and have significant clinical implications for the treatment of children with DM.
Conditions
- Juvenile Dermatomyositis
Interventions
- DIETARY_SUPPLEMENT
-
Creapure
Patients will be prescribed a creapure supplement by weight, to be taken 3x/day for the duration of the trial. They will be randomized to an active product start time using a multiple baseline design.
- DIETARY_SUPPLEMENT
-
Glucose Tablet
Patients will be prescribed the placebo supplement by weight, to be taken 3x/day for the duration of the trial. They will be randomized to an active product start time using a multiple baseline design.
Sponsors & Collaborators
-
The Hospital for Sick Children
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- QUADRUPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 7 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-03-31
- Primary Completion
- 2017-05-31
- Completion
- 2017-05-31
Countries
- Canada
Study Locations
More Related Trials
-
Extension Study of NS-065/NCNP-01 in Boys With Duchenne Muscular Dystrophy (DMD)
NCT03167255 ·Status: COMPLETED ·Phase: PHASE2
-
L-citrulline and Metformin in Duchenne's Muscular Dystrophy
NCT01995032 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Muscle Wasting and Altered Metabolism in Patients With Myotonic Dystrophy
NCT00004769 ·Status: COMPLETED
-
Effect of Creatine Monohydrate on Functional Muscle Strength in Children With FSHD
NCT02948244 ·Status: COMPLETED ·Phase: NA
-
Creatine Safety, Tolerability, & Efficacy in Huntington's Disease (CREST-E)
NCT00712426 ·Status: TERMINATED ·Phase: PHASE3
-
High-dose Prednisone in Duchenne Muscular Dystrophy
NCT00110669 ·Status: COMPLETED ·Phase: PHASE3
-
Home-based Training and Supplementation in DM1 Patients
NCT05848830 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Effect of Oral Glutamine on Muscle Mass and Function in Duchenne Muscular Dystrophy
NCT00296621 ·Status: COMPLETED ·Phase: PHASE2
-
Validating Cardiac MRI Biomarkers and Genotype-Phenotype Correlations for DMD
NCT02834650 ·Status: COMPLETED ·Phase: NA
-
Clinical Trial of Creatine in Amyotrophic Lateral Sclerosis
NCT00005766 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy Study of Recombinant Human Insulin-Like Growth Factor-I/Recombinant Human Insulin-Like Growth Factor Binding Protein-3 (rhIGF-I/rhIGFBP-3) In Myotonic Dystrophy Type 1
NCT00577577 ·Status: COMPLETED ·Phase: PHASE2
-
Improved Muscle Function in Duchenne Muscular Dystrophy Through L-Arginine and Metformin
NCT02516085 ·Status: COMPLETED ·Phase: PHASE1
-
Pilot Compassionate Use Study of Thioctic Acid Treatment in Mitochondrial Myopathy
NCT00004770 ·Status: COMPLETED ·Phase: NA
-
Studying Skeletal Muscle, Heart, and Diaphragm Imaging in Boys With Duchenne Muscular Dystrophy
NCT01451281 ·Status: COMPLETED
-
Phase I/II Study of SRP-4053 in DMD Patients
NCT02310906 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Clinical Trial Readiness for the Dystroglycanopathies
NCT00313677 ·Status: RECRUITING
-
An Observational Study Comparing Delandistrogene Moxeparvovec (ELEVIDYS) With Standard of Care in Participants With Duchenne Muscular Dystrophy
NCT06270719 ·Status: ENROLLING_BY_INVITATION
-
Extracellular RNA Biomarkers of Duchenne Muscular Dystrophy
NCT05016908 ·Status: RECRUITING
-
Exploratory Study of NS-065/NCNP-01 in DMD
NCT02081625 ·Status: COMPLETED ·Phase: PHASE1
-
The Baby Duchenne Study: Characterizing Developmental and Clinical Outcomes in the First Three Years in Children With Duchenne Muscular Dystrophy
NCT07092540 ·Status: RECRUITING
-
Safety Study of Mini-dystrophin Gene to Treat Duchenne Muscular Dystrophy
NCT00428935 ·Status: COMPLETED ·Phase: PHASE1
-
Creatine for the Treatment of Amyotrophic Lateral Sclerosis
NCT00070993 ·Status: COMPLETED ·Phase: PHASE2
-
Twice Weekly Steroids and Exercise as Therapy for DMD
NCT04322357 ·Status: COMPLETED ·Phase: PHASE2
-
NS-050/NCNP-03 in Boys With DMD (Meteor50)
NCT06053814 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Clinical Trial of Creatine in Amyotrophic Lateral Sclerosis [ALS]
NCT00005674 ·Status: COMPLETED ·Phase: PHASE2