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Gabapentin Versus Estrogen for the Treatment of Hot Flashes

Primary Purpose

Hot Flashes

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Gabapentin, Estrogen and placebo administration
Sponsored by
University of Rochester
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hot Flashes focused on measuring Hot flashes, postmenopausal, climacteric symptoms, hormone replacement therapy, gabapentin

Eligibility Criteria

35 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Menopausal women between ages 35-60 Must experience 7-20, moderate-severe hot flashes/day or 50-140 moderate-severe hot flashes/week for greater than two months Must have had a bilateral salpingo-oopherectomy for >12 months or amenorrhea>6 months or #4 (below) Has an FSH>30 mIU/ml Must have a signed informed consent Able to function independent in all activities of daily living and be capable of reliable documentation Exclusion Criteria: Any contraindication to estrogen and progesterone replacement therapy History of an MI, stroke, and/or functional decline. Fails to record data in the hot flash diary>3 days during the 2 week baseline period. Unable or willing to make required visits at the specified times over the course of therapy. History of any malignancies or undiagnosed vaginal bleeding. History of chronic liver, gallbladder, chronic renal, cardiac or endocrine diseases

Sites / Locations

  • University of Rochester

Outcomes

Primary Outcome Measures

Reduction in hot flash frequency

Secondary Outcome Measures

Side effects
Effect on climacteric symptoms
Effect on depression

Full Information

First Posted
January 11, 2006
Last Updated
November 27, 2006
Sponsor
University of Rochester
Collaborators
National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00276081
Brief Title
Gabapentin Versus Estrogen for the Treatment of Hot Flashes
Official Title
A Randomized Trial of Gabapentin, Estrogen and Placebo for the Treatment of Postmenopausal Hot Flashes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2006
Overall Recruitment Status
Completed
Study Start Date
May 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2004 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Rochester
Collaborators
National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

5. Study Description

Brief Summary
To compare the efficacy and safety of gabapentin, estrogen and placebo in the treatment of hot flashes and other climacteric symptoms.
Detailed Description
HRT is associated with an increased risk of thrombo-embolic events, breast cancer and cardiovascular events. Safe, effective, and well-tolerated alternative therapies for hot flashes are needed. Gabapentin is a gamma-aminobutyric acid (GABA)-analog that we have reported is associated with a reduction in the frequency of hot flashes in postmenopausal women who were taking gabapentin for other indications. However, it is not known whether the efficacy of gabapentin in the treatment of hot flashes and other menopausal symptoms is comparable to that of estrogen, the gold standard. For this study, 60 subjects are to be recruited and randomized into 3 arms of 20 each (gabapentin, estrogen and placebo).We will perform an analysis of the results after all 60 subjects have been recruited, screened, enrolled and completed the study. The investigators of the study continue to be blinded to the study groups and their randomization. To determine if gabapentin approaches the efficacy of estrogen in the treatment of hot flashes,postmenopausal women between ages 35 and 60 with 7-20 moderate-severe postmenopausal hot flashes/day will be randomized into a double-blinded placebo controlled trial of estrogen, gabapentin and placebo. All patients must meet stringent inclusion and exclusion criteria. Pre- and post-study hot flash diaries, depression and climacteria scales will be collected. Patients are required to undergo physical examination and blood work and to complete a daily hot flash and medication compliance records. Hot flash frequency and composite score for hot flashes will be calculated for the three groups based on the hot flash diary. Side effects, climacteric scale and depression scales will also be used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hot Flashes
Keywords
Hot flashes, postmenopausal, climacteric symptoms, hormone replacement therapy, gabapentin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Gabapentin, Estrogen and placebo administration
Primary Outcome Measure Information:
Title
Reduction in hot flash frequency
Secondary Outcome Measure Information:
Title
Side effects
Title
Effect on climacteric symptoms
Title
Effect on depression

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Menopausal women between ages 35-60 Must experience 7-20, moderate-severe hot flashes/day or 50-140 moderate-severe hot flashes/week for greater than two months Must have had a bilateral salpingo-oopherectomy for >12 months or amenorrhea>6 months or #4 (below) Has an FSH>30 mIU/ml Must have a signed informed consent Able to function independent in all activities of daily living and be capable of reliable documentation Exclusion Criteria: Any contraindication to estrogen and progesterone replacement therapy History of an MI, stroke, and/or functional decline. Fails to record data in the hot flash diary>3 days during the 2 week baseline period. Unable or willing to make required visits at the specified times over the course of therapy. History of any malignancies or undiagnosed vaginal bleeding. History of chronic liver, gallbladder, chronic renal, cardiac or endocrine diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sireesha Y. Reddy, M.D.
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Rochester
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16816054
Citation
Reddy SY, Warner H, Guttuso T Jr, Messing S, DiGrazio W, Thornburg L, Guzick DS. Gabapentin, estrogen, and placebo for treating hot flushes: a randomized controlled trial. Obstet Gynecol. 2006 Jul;108(1):41-8. doi: 10.1097/01.AOG.0000222383.43913.ed.
Results Reference
result

Learn more about this trial

Gabapentin Versus Estrogen for the Treatment of Hot Flashes

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