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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UNKNOWN
NA
60 participants
INTERVENTIONAL
2010-09-30
2011-02-28
Brief Summary
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Detailed Description
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* Intervention: Over an four-week period, the treatment group (n=30) uses capsaicin patch (100 mcg/3cc) at the tender point of neck for 12 hours a day; the control group (n=30) receives Hydrogel patch instead of capsaicin patch.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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capsaicin patch
Capsaicin patch
Over an four-week period, the treatment group (n=30) uses capsaicin patch (100 mcg/3cc) at the tender point of neck for 12 hours a day; the control group (n=30) receives Hydrogel patch instead of capsaicin patch.
Hydrogel patch
Capsaicin patch
Over an four-week period, the treatment group (n=30) uses capsaicin patch (100 mcg/3cc) at the tender point of neck for 12 hours a day; the control group (n=30) receives Hydrogel patch instead of capsaicin patch.
Interventions
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Capsaicin patch
Over an four-week period, the treatment group (n=30) uses capsaicin patch (100 mcg/3cc) at the tender point of neck for 12 hours a day; the control group (n=30) receives Hydrogel patch instead of capsaicin patch.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
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Kyunghee University Medical Center
OTHER
Responsible Party
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College of Oriental Medicine, Kyung Hee University
Principal Investigators
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Mi-Yeon Song, OMD, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Oriental Rehabilitation Medicine/College of Oriental Medicine/Kyung Hee University
Locations
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Kyunghee University East West Neo Medical Center
Seoul, , South Korea
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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KHU 20100675
Identifier Type: -
Identifier Source: org_study_id