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Endometriosis : Traditional Medicine vs Hormone Therapy

Primary Purpose

Endometriosis, Pelvic Pain

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Chinese Products
Nafarelin
Sponsored by
National Center for Complementary and Integrative Health (NCCIH)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometriosis focused on measuring Endometriosis, Pelvic pain, Acupuncture, Chinese herbs, Hormone therapy, Nafarelin

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Women with laparoscopy-confirmed endometriosis within the past 6 years Experiencing chronic pelvic pain, dysmenorrhea (painful periods) and dyspareunia (painful intercourse), at least one of which is moderate to severe Exclusion Criteria: Use of traditional Chinese medicine for endometriosis. If previous treatment with hormone therapy, must have responded positively but not have been on hormone therapy within the past 6 months Use of any form of hormone-based contraception during the 12-week treatment and 24-week follow-up periods Diagnosed with any chronic condition other than endometriosis, or any other acute condition that causes pain Pregnancy or breast feeding

Sites / Locations

  • Oregon Health Sciences University, Women's Health Research Unit
  • Oregon College of Oriental Medicine Clinic

Outcomes

Primary Outcome Measures

Pain assessments

Secondary Outcome Measures

Full Information

First Posted
April 19, 2002
Last Updated
January 23, 2008
Sponsor
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00034047
Brief Title
Endometriosis : Traditional Medicine vs Hormone Therapy
Official Title
Endometriosis : Traditional Medicine vs Hormone Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
August 2006 (Actual)
Study Completion Date
August 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

5. Study Description

Brief Summary
This 36-week study will determine whether traditional Chinese medicine (acupuncture and Chinese herbs) is as effective as hormone therapy for alleviating endometriosis-related pelvic pain.
Detailed Description
Endometriosis is a significant public health problem affecting 10-15% of women of childbearing age, many of whom suffer persistent pelvic pain and infertility. Therapeutic options include surgery and hormone therapy that are often temporarily effective but produce unwanted side-effects. The present proposal, based on case series reports of the effectiveness of Traditional Chinese Medicine (TCM: acupuncture and Chinese herbs) for this condition, aims to evaluate whether TCM is as effective as hormone therapy for alleviating endometriosis-related chronic pain. Women with laparoscopy-diagnosed endometriosis will be randomly assigned to either TCM or hormone therapy. Women assigned to TCM will be divided into four sub-groups on the basis of the diagnostic categories of endometriosis recognized by TCM. A pre-established acupuncture protocol and herbal formula specific for each sub-group will be followed. This aspect of the research design permits an important feature of the clinical practice of TCM (matching treatment to sub-group diagnosis) to be adopted in a clinical trial. Women assigned to hormone therapy will be treated with the gonadotropin releasing hormone agonist (GnRHa), nafarelin, chosen for this study on the basis of its clinical trial-established efficacy, ease of patient usage via intranasal spray and milder side-effect profile relative to other GnRHa's. Pelvic pain symptoms (patient-scored) and signs (physician-scored) will be assessed at baseline, after 12 weeks of treatment, and at 12- and 24-week post-treatment follow-up. Pelvic examination scores will be determined by a physician blinded to the treatment group assignments. Side effects, including those of pseudomenopause known to result from GnRHa therapy, will be recorded in both groups at 4-week intervals during the 12-week treatment, and at each follow-up time. A further objective is to make a preliminary assessment of whether diagnostic sub-groups of endometriosis recognized by TCM serve as predictors of differential response to hormone therapy. Data obtained from this study, on treatment effectiveness, side effect profiles, recurrence of symptoms, compliance with therapy and drop-out rates, will be used to design a large-scale clinical trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis, Pelvic Pain
Keywords
Endometriosis, Pelvic pain, Acupuncture, Chinese herbs, Hormone therapy, Nafarelin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Acupuncture
Intervention Type
Drug
Intervention Name(s)
Chinese Products
Intervention Type
Drug
Intervention Name(s)
Nafarelin
Primary Outcome Measure Information:
Title
Pain assessments

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women with laparoscopy-confirmed endometriosis within the past 6 years Experiencing chronic pelvic pain, dysmenorrhea (painful periods) and dyspareunia (painful intercourse), at least one of which is moderate to severe Exclusion Criteria: Use of traditional Chinese medicine for endometriosis. If previous treatment with hormone therapy, must have responded positively but not have been on hormone therapy within the past 6 months Use of any form of hormone-based contraception during the 12-week treatment and 24-week follow-up periods Diagnosed with any chronic condition other than endometriosis, or any other acute condition that causes pain Pregnancy or breast feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Hammerschlag, PhD
Organizational Affiliation
Oregon College of Oriental Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kenneth Burry, MD
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oregon Health Sciences University, Women's Health Research Unit
City
Portland
State/Province
Oregon
ZIP/Postal Code
97201
Country
United States
Facility Name
Oregon College of Oriental Medicine Clinic
City
Portland
State/Province
Oregon
ZIP/Postal Code
97216
Country
United States

12. IPD Sharing Statement

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Endometriosis : Traditional Medicine vs Hormone Therapy

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