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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
See also
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Recruiting NCT06030388 - Strength and Aerobic Training Against Hot Flushes in Postmenopausal Women N/A
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Active, not recruiting NCT05086705 - EMBr Wave for the Reduction of Hot Flashes in Women With a History of Breast Cancer N/A
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
Completed NCT01140646 - Evaluation of SAMe for Hot Flashes Phase 2