The Efficacy of Using Far Infrared Radiation to Manage Muscular Dystrophies
Phase 1 Study to Determine the Efficacy of Using Far Infrared Radiation to Manage or Treat Muscular Dystrophies.
1 other identifier
interventional
4
1 country
1
Brief Summary
The muscular dystrophies (MD) are a group of more than 30 neuromuscular disorders that are characterized by progressive skeletal muscle weakness, defects in muscle proteins and the death of muscle cells and tissue. This study will investigate the use of far infrared radiation for managing muscular dystrophies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started May 2008
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2008
CompletedFirst Submitted
Initial submission to the registry
May 6, 2008
CompletedFirst Posted
Study publicly available on registry
May 8, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedAugust 17, 2009
August 1, 2009
2 years
May 6, 2008
August 14, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Management and Cure of muscular dystrophies
2 Years
Secondary Outcomes (1)
Rehabilitation of people with muscular dystrophies
2 Years
Study Arms (1)
1
EXPERIMENTALRadiation: Far Infrared Radiation (5μm to 20μm wavelength)
Interventions
Radiation: Far Infrared Radiation (5μm to 20μm wavelength) Far Infrared radiation for 30 to 40 minutes per treatment session.
Eligibility Criteria
You may qualify if:
- Persons with muscular dystrophies
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Centre for Incurable Diseases
Toronto, Ontario, M4V 1L5, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ken Nedd, M.D.
GAAD Medical Research Institute Inc.
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 6, 2008
First Posted
May 8, 2008
Study Start
May 1, 2008
Primary Completion
May 1, 2010
Study Completion
June 1, 2010
Last Updated
August 17, 2009
Record last verified: 2009-08