Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE2/PHASE3
3 participants
INTERVENTIONAL
2008-01-31
2008-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Acupuncture
Traditional Chinese acupuncture in conjunction with standard medical care
traditional Chinese acupuncture
10 treatments over 6 weeks
Standard medical care
standard medical care
standard medical care
standard care as provided by primary physician
Interventions
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traditional Chinese acupuncture
10 treatments over 6 weeks
standard medical care
standard care as provided by primary physician
Eligibility Criteria
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Inclusion Criteria
* 21 days or less between start of symptoms and diagnostic test
* presence of fatigue of at least 4/11 (by Chalder Fatigue Questionnaire)
* no other illnesses present
* meets residency requirement
Exclusion Criteria
* unable to begin acupuncture within 21 days of diagnostic test
* acupuncture use currently or in the preceding 3 months
* currently under the care of a TCM practitioner
* unwilling to be randomized
15 Years
25 Years
ALL
No
Sponsors
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University of Alberta
OTHER
Responsible Party
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Principal Investigators
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Sunita Vohra, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
University of Alberta
Locations
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University of Alberta
Edmonton, Alberta, Canada
Countries
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Other Identifiers
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6866
Identifier Type: -
Identifier Source: org_study_id
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