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| Sponsor: | Mayo Clinic |
|---|---|
| Information provided by: | Mayo Clinic |
| ClinicalTrials.gov Identifier: | NCT00217074 |
Purpose
Methods: 103 participants, after being randomized to medical versus sham acupuncture received bi-weekly treatments for 5 weeks, after a baseline assessment week. They were then followed for an additional 7 weeks. Participants completed daily hot flash questionnaires, which formed the basis for analysis.
| Condition | Intervention | Phase |
|---|---|---|
|
Hot Flashes |
Other: acupuncture |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind Primary Purpose: Treatment |
| Official Title: | Acupuncture for Hot Flashes: A Randomized Sham Controlled Clinical Study |
Eligibility| Ages Eligible for Study: | 45 Years to 59 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Participants eligible for this study were females aged 45 to 59 with a reported average of ¡Ý 5 hot flashes a day
Contacts and Locations
More Information
| ClinicalTrials.gov Identifier: | NCT00217074 History of Changes |
| Other Study ID Numbers: | 2294-03 |
| Study First Received: | September 20, 2005 |
| Last Updated: | February 1, 2010 |
| Health Authority: | United States: Institutional Review Board |
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Hot Flashes Signs and Symptoms |