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Acupunture and Hot Flashes
This study is ongoing, but not recruiting participants.
First Received: September 20, 2005   No Changes Posted
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
Procedure: Acupuncture
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Placebo Control, Single Group Assignment, Efficacy Study
Official Title: Acupuncture for Hot Flashes: A Randomized Sham -Controlled Clinical Study.

Resource links provided by NLM:


Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • Hot Flash Score

Estimated Enrollment: 103
Study Start Date: January 2004
  Eligibility

Ages Eligible for Study:   45 Years to 59 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Participants eligible for this study were females aged 45 to 59 with a reported average of greater than 5 hot flashes a day.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00217074

Locations
United States, Minnesota
Mayo Clinic
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
Investigators
Principal Investigator: Ann Vincent, MBBS, M.D. Mayo Clinic
  More Information

No publications provided

Study ID Numbers: IRB 2294-03
Study First Received: September 20, 2005
Last Updated: September 20, 2005
ClinicalTrials.gov Identifier: NCT00217074     History of Changes
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Signs and Symptoms
Hot Flashes

ClinicalTrials.gov processed this record on November 20, 2009