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Efficacy Study of Raloxifene to Induce Ovulation in Polycystic Ovarian Syndrome (PCOS)

Primary Purpose

Polycystic Ovarian Syndrome

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Raloxifene
Clomiphene
Sponsored by
Bruce Lessey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovarian Syndrome focused on measuring PCOS, Infertility, Anovulation

Eligibility Criteria

18 Years - 36 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Women aged 18 to 36
  2. BMI > 19 & < 40
  3. PCOS diagnosis as evidenced by:

Oligo- and/or anovulation (< 6 cycles per year) and one of the following:

  • Clinical and/or biochemical signs of hyperandrogenism
  • Polycystic ovaries and exclusion of other aetiologies (congenital adrenal hyperplasias, androgen-secreting tumors, Cushing's syndrome)

Exclusion Criteria:

  1. Use of ovulation induction agents within the past 6 months
  2. Positive pregnancy test before taking study medications
  3. History or current thromboembolic disorder
  4. Coronary artery disease such as heart attack or stroke
  5. Tobacco use or history within the past 6 months
  6. History of pelvic inflammatory disease and tubal factor infertility
  7. Congenital adrenal hyperplasia
  8. Diabetes Mellitus

    • Any subject on Metformin must "wash out" for 30 days prior to screening
  9. History of endometriosis
  10. Known male factor infertility

Sites / Locations

  • Greenville Hospital System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Raloxifene

Clomiphene

Arm Description

3 cycles of 120mg/day of Evista (raloxifene) on days 3 to 7

3 cycles of 100mg/day of Clomid (clomiphene citrate) on days 3 to 7

Outcomes

Primary Outcome Measures

Pregnancy
Time frame will vary depending on how many treatment cycles it takes to get pregnant. If no pregnancy occurs, study participation will likely be about 4 months.

Secondary Outcome Measures

Ovulation
If ovulation does not occur during the first treatment cycle, subject will be withdrawn from study.

Full Information

First Posted
February 15, 2012
Last Updated
August 21, 2018
Sponsor
Bruce Lessey
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1. Study Identification

Unique Protocol Identification Number
NCT01607320
Brief Title
Efficacy Study of Raloxifene to Induce Ovulation in Polycystic Ovarian Syndrome
Acronym
PCOS
Official Title
Effect of Raloxifene on Ovulation in Women With Polycystic Ovarian Syndrome.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Terminated
Why Stopped
Over budget, slow recruitment, and personnel change
Study Start Date
June 2012 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
March 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Bruce Lessey

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study examines Raloxifene versus Clomiphene to induce ovulation in women with polycystic ovarian syndrome (PCOS).
Detailed Description
Clomiphene citrate (CC) is the major pharmaceutical treatment of anovulation in polycystic ovary syndrome, used for over 40 years. Despite the vast experience using this drug, the pregnancy rates associated with its use are low and recent large studies from Australia regarding birth defects suggest that CC may be associated with birth defects. Alternatives to CC are limited. Another selective estrogen receptor modulator, Raloxifene (RAL) does not have the long half life exhibited by CC, and has recently been shown to be equivalent to CC in terms of ability to induce ovulation in PCOS women. In addition, prior studies have demonstrated potential benefits on markers of uterine receptivity in a cell line model by blocking estrogen activity. Beyond this, there are no studies to examine whether Raloxifene is an effective oral agent for the treatment of women desiring pregnancy, but the investigators' hypothesis is that Raloxifene will work as well as CC but be better at establishment and maintenance of pregnancy than CC

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovarian Syndrome
Keywords
PCOS, Infertility, Anovulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Raloxifene
Arm Type
Experimental
Arm Description
3 cycles of 120mg/day of Evista (raloxifene) on days 3 to 7
Arm Title
Clomiphene
Arm Type
Active Comparator
Arm Description
3 cycles of 100mg/day of Clomid (clomiphene citrate) on days 3 to 7
Intervention Type
Drug
Intervention Name(s)
Raloxifene
Other Intervention Name(s)
Provera
Intervention Description
Thirty PCOS patients treated with 3 cycles of 120mg/day of Evista (raloxifene) on days 3 to 7 following an initial provera withdrawal
Intervention Type
Drug
Intervention Name(s)
Clomiphene
Other Intervention Name(s)
Provera
Intervention Description
Thirty PCOS patients treated with 3 cycles of 100mg/day of Clomid (clomiphene citrate) on days 3 to 7 following an initial provera withdrawal
Primary Outcome Measure Information:
Title
Pregnancy
Description
Time frame will vary depending on how many treatment cycles it takes to get pregnant. If no pregnancy occurs, study participation will likely be about 4 months.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Ovulation
Description
If ovulation does not occur during the first treatment cycle, subject will be withdrawn from study.
Time Frame
Cycle day 22-24

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
36 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women aged 18 to 36 BMI > 19 & < 40 PCOS diagnosis as evidenced by: Oligo- and/or anovulation (< 6 cycles per year) and one of the following: Clinical and/or biochemical signs of hyperandrogenism Polycystic ovaries and exclusion of other aetiologies (congenital adrenal hyperplasias, androgen-secreting tumors, Cushing's syndrome) Exclusion Criteria: Use of ovulation induction agents within the past 6 months Positive pregnancy test before taking study medications History or current thromboembolic disorder Coronary artery disease such as heart attack or stroke Tobacco use or history within the past 6 months History of pelvic inflammatory disease and tubal factor infertility Congenital adrenal hyperplasia Diabetes Mellitus Any subject on Metformin must "wash out" for 30 days prior to screening History of endometriosis Known male factor infertility
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruce A. Lessey, MD, PhD
Organizational Affiliation
Greenville Hospital System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Greenville Hospital System
City
Greenville
State/Province
South Carolina
ZIP/Postal Code
29605
Country
United States

12. IPD Sharing Statement

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Efficacy Study of Raloxifene to Induce Ovulation in Polycystic Ovarian Syndrome

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