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NCT00217074 Clinical Trial

Acupuncture and Hot Flashes

Hot Flashes Clinical Trial

Official title:
Acupuncture for Hot Flashes: A Randomized Sham Controlled Clinical Study

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00217074
Other study ID # 2294-03
Secondary ID
Status Terminated
Phase Phase 3
First received September 20, 2005
Last updated February 1, 2010
Start date January 2004
Est. completion date October 2005

Study information
Verified date February 2010
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Terminated
Enrollment 103
Est. completion date October 2005
Est. primary completion date January 2004
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 45 Years to 59 Years
Eligibility Participants eligible for this study were females aged 45 to 59 with a reported average of ¡Ý 5 hot flashes a day

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Other:
• acupuncture

Locations
Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hot Flash Score
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Completed NCT05099159 - A Study to Learn More About How Well Elinzanetant Works and How Safe it is for the Treatment of Vasomotor Symptoms (Hot Flashes) That Are Caused by Hormonal Changes Over 26 Weeks in Women Who Have Been Through the Menopause (OASIS-2) Phase 3
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