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Clinical Trials/NCT00284492
NCT00284492
Completed
Not Applicable

Effectiveness of Acupuncture-care for Treatment of Hot Flushes Among Postmenopausal Women

University Hospital of North Norway1 site in 1 country286 target enrollmentFebruary 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Menopause
Sponsor
University Hospital of North Norway
Enrollment
286
Locations
1
Primary Endpoint
Frequency of hot flushes
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

In a pragmatic study investigate whether Traditional Chinese Medicine acupuncture-care decreases the frequency of hot flushes and increases health related quality of life among postmenopausal women. The intervention group will receive 10 sessions of acupuncture, the control group will engage in self care only. The study period lasts for 12 weeks.

Detailed Description

The study objective is to determine whether Traditional Chinese Medicine (TCM) acupuncture-care together with self-care is more effective than self-care alone, to relieve climacteric complaints among women who seek alternatives to hormonal replacement therapy (HRT). Study design is a pragmatic randomised controlled trial with two parallel arms. Study participants are postmenopausal women who document a mean value of 7 flushes/24 hours and who are not using HRT or other prescribed medication that may influence climacteric complaints. The treatment group will receive 10 sessions of TCM acupuncture-care and self-care; the control group will engage in self-care only. The duration of intervention period is 12 weeks with evaluations at baseline, 4, 8, 12 weeks, and follow up at 6 and 12 months after baseline. Primary endpoint is change in daily hot flush frequency in the two groups from baseline to 12 weeks; secondary endpoint is health related quality of life. N in each treatment group: 143 (286 altogether).

Registry
clinicaltrials.gov
Start Date
February 2006
End Date
May 2008
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University Hospital of North Norway
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Postmenopausal women (at least one year past the last menstrual period) who are willing to receive acupuncture and who during two weeks of self-completed diaries10 document a mean value of 7 flushes/24 hours or more (or 50 flushes or more over a period of seven consecutive days), will be randomized after a baseline evaluation.
  • Current users prescribed medications that influence hot flush rate (e. g. HRT, SSRI's) can be included after a washout period. The washout-periods are eight weeks for SSRI's and systemic (including transdermal) HRT and four weeks for local estradiol preparations

Exclusion Criteria

  • Surgical menopause
  • History of cancer within the past five years
  • Use of anticoagulant drugs
  • Heart valve disease
  • Poorly controlled hypertension
  • Hypothyroidism
  • Hyperthyroidism or diabetes mellitus
  • Organ transplant
  • Mental disease
  • Overt drug or alcohol dependency

Outcomes

Primary Outcomes

Frequency of hot flushes

Time Frame: 12 weeks

Secondary Outcomes

  • Health related quality of life (Women's Health Questionnaire)(12 weeks)

Study Sites (1)

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