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Ovulation Induction With Clomiphene Citrate and Dexamethasone

Primary Purpose

Infertility

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Placebo
Dexamethasone
Sponsored by
San Antonio Military Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring ovulation induction, dexamethasone

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Active duty military members or dependents seeking infertility treatment at Brooke Army Medical Center
  • primary or secondary infertility
  • candidate for intrauterine insemination (IUI)

Exclusion Criteria:

  • Severe male factor infertility (total motile sperm count <10 million/mL)
  • Bilateral fallopian tube obstruction
  • Diminished ovarian reserve (baseline follicle stimulating hormone > 20)
  • History of clomiphene resistance as determined by a Clomid challenge test or prior non-ovulatory cycles while taking clomiphene
  • Known or suspected hypopituitarism or hypothalamic amenorrhea
  • Six or more prior therapeutic CC cycles without a pregnancy
  • Diabetes
  • Renal impairment, hepatitis, hepatic cirrhosis, or myasthenia gravis
  • Osteoporosis
  • Cataracts or glaucoma
  • Congenital Adrenal Hyperplasia, Cushing's disease, or any condition requiring chronic corticosteroid use

Sites / Locations

  • San Antonio Military Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Clomiphene plus dexamethasone

Clomiphene plus placebo

Arm Description

Oral dexamethasone will be added to clomiphene citrate

A placebo of dexamethasone will be given with clomiphene citrate

Outcomes

Primary Outcome Measures

Pregnancy
Determined by serum hCG measurement

Secondary Outcome Measures

Clinical pregnancy
Determined by ultrasound

Full Information

First Posted
March 19, 2013
Last Updated
February 27, 2014
Sponsor
San Antonio Military Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01856062
Brief Title
Ovulation Induction With Clomiphene Citrate and Dexamethasone
Official Title
Ovulation Induction With Clomiphene Citrate and Dexamethasone
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2013 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
San Antonio Military Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if the addition of dexamethasone to clomiphene citrate will increase the pregnancy rate of intrauterine insemination (IUI) cycles.
Detailed Description
For decades clomiphene citrate (CC) has been the first line therapy for ovulation induction in anovulatory or oligoovulatory women, and for superovulation in women with unexplained infertility or partners with mild sperm abnormalities. While approximately 80% of patients achieve ovulation with CC, less than half conceive. Pregnancy is achieved in approximately 10% of ovulatory cycles. Addition of dexamethasone to CC has been shown to result in pregnancy rates of 21-40% in CC-resistant women (defined as patients failing to ovulate on CC alone). A subsequent randomized controlled trial demonstrated higher pregnancy rates in patients with unexplained infertility undergoing intrauterine insemination (IUI) with CC + dexamethasone compared to those taking CC alone. In light of the relatively high pregnancy rates achieved in previous trials, we hypothesize that dexamethasone as an adjunct to CC will increase the ovulation rate and pregnancy rate for all appropriate candidates for IU with a standard CC regimen. Our study is designed to randomize patients undergoing ovulation induction with IUI into two groups: one consisting of a standard CC regimen, and the other consisting of the same CC regimen with the addition of daily dexamethasone. The primary outcome measure is pregnancy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
ovulation induction, dexamethasone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Clomiphene plus dexamethasone
Arm Type
Experimental
Arm Description
Oral dexamethasone will be added to clomiphene citrate
Arm Title
Clomiphene plus placebo
Arm Type
Placebo Comparator
Arm Description
A placebo of dexamethasone will be given with clomiphene citrate
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
sugar pill
Intervention Description
A placebo with similar appearance to dexamethasone will be given with a standard regimen of clomiphene citrate (100mg/day oral for 5 days) for ovulation induction
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
Oral dexamethasone will be added to a standard regimen of clomiphene citrate (100mg/day oral for 5 days) for ovulation induction
Primary Outcome Measure Information:
Title
Pregnancy
Description
Determined by serum hCG measurement
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Clinical pregnancy
Description
Determined by ultrasound
Time Frame
12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active duty military members or dependents seeking infertility treatment at Brooke Army Medical Center primary or secondary infertility candidate for intrauterine insemination (IUI) Exclusion Criteria: Severe male factor infertility (total motile sperm count <10 million/mL) Bilateral fallopian tube obstruction Diminished ovarian reserve (baseline follicle stimulating hormone > 20) History of clomiphene resistance as determined by a Clomid challenge test or prior non-ovulatory cycles while taking clomiphene Known or suspected hypopituitarism or hypothalamic amenorrhea Six or more prior therapeutic CC cycles without a pregnancy Diabetes Renal impairment, hepatitis, hepatic cirrhosis, or myasthenia gravis Osteoporosis Cataracts or glaucoma Congenital Adrenal Hyperplasia, Cushing's disease, or any condition requiring chronic corticosteroid use
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brandy M Butler, MD
Phone
210-916-2168
Email
brandy.m.butler2.mil@mail.mil
First Name & Middle Initial & Last Name or Official Title & Degree
Jamie Massie, MD
Phone
210-916-5335
Email
jamie.a.massie2.mil@mail.mil
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jamie Massie, MD
Organizational Affiliation
San Antonio Military Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
San Antonio Military Medical Center
City
Ft. Sam Houston
State/Province
Texas
ZIP/Postal Code
78234
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jay R Bucci, MD
Phone
210-916-2598
Email
jay.r.bucci.mil@mail.mil
First Name & Middle Initial & Last Name & Degree
Jamie Massie, MD

12. IPD Sharing Statement

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Ovulation Induction With Clomiphene Citrate and Dexamethasone

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