Clomiphene Citrate Plus Cabergoline in Treatment of Polycystic Ovary Syndrome
Primary Purpose
Female Reproductive Problem
Status
Unknown status
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Clomiphene citrate
Cabergoline
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Female Reproductive Problem
Eligibility Criteria
Inclusion Criteria:
- 2 or more of PCOS signs according to Rotterdam diagnostic criteria (2003).-
- Primary or secondary infertility.-
- Absence of galactorrhoea
- Normal serum prolactin or slightly elevated (up to 50 ng/dl)
- Normal hysterosalpingography
- Normal spermogram
Exclusion Criteria:
- Women on other line of treatment as aromatase inhibitors, gonadotrophins, or tamoxifen.
- Known hypersensitivity for Clomiphene citrate or cabergoline.
- Other factors of infertility as tubal factor, uterine factor or male factor.
Sites / Locations
- Assiut universityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Clomiphene citrate plus cabergoline
Clomiphene citrate plus placebo
Arm Description
This group will receive Clomiphene citrate 50 mg tablet twice daily from the second day of menses to the sixth day plus cabergoline 0.25 mg from second day every 3 days (4 doses only)
This group will receive Clomiphene citrate 50 mg tablet twice daily from the second day of menses to the sixth day plus placebo tablets from second day every 3 days (4 doses only)
Outcomes
Primary Outcome Measures
Size of mature follicles (mm).
Secondary Outcome Measures
Number of pregnancy
Number of mature follicles (mm)
Full Information
NCT ID
NCT02644304
First Posted
October 13, 2015
Last Updated
June 28, 2016
Sponsor
Woman's Health University Hospital, Egypt
1. Study Identification
Unique Protocol Identification Number
NCT02644304
Brief Title
Clomiphene Citrate Plus Cabergoline in Treatment of Polycystic Ovary Syndrome
Official Title
Clomiphene Citrate Plus Cabergoline Versus Clomiphene Citrate Alone in Treatment of Polycystic Ovary Syndrome Associated Infertility
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Unknown status
Study Start Date
May 2015 (undefined)
Primary Completion Date
October 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Woman's Health University Hospital, Egypt
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Polycystic ovary syndrome (PCOS) is the most common endocrine disorder of reproductive aged women and affects approximately 5-12 % of the female population.
In 2003 in Rotterdam , Rotterdam diagnostic criteria were redefined PCOS as affected individuals must have two out of the following three criteria:
Oligo- and/or anovulation, (ovulation occurs less than once every 35 days).
Hyperandrogenism, clinical signs include hirsutism, acne, alopecia, and frank virilization, while chemical indicators include raised concentrations of total testosterone and androstenedione , and elevated free androgen index.
Polycystic ovaries on sonographic examination, presence of 12 or more follicles in either ovary measuring 2-9 mm in diameter, increased ovarian volume more than 10 cm3 and/or increase in stromal echogenicity. Clearly, according to the Rotterdam diagnostic criteria, the majority of women with PCOS can be diagnosed without the need of laboratory examinations.
Clomiphene citrate (CC) is still the first-line medication for the induction of ovulation. It is an anti-estrogenic compound made up of two isomers, enclomiphene and zuclomiphene; the latter being the more potent of the two. It is a non-steroidal compound closely resembling estrogen. CC acts by blocking estrogen receptors, particularly in the hypothalamus, thereby signaling a lack of circulating estrogens and inducing a change in the pulsatile release of gonadotrophin-releasing hormone (GnRH). This induces release of follicle stimulating hormone from the anterior pituitary and is often enough to set the cycle of events leading to ovulation into motion.
Cabergoline, ergot-derived dopamine agonists with a very long half life, is an effective prolactin suppressor. Cabergoline oral administration contains a weekly dose of 0.5 - 3 mg, which could be increased, if needed, to twice a week. This medicine has slight dopamine agonistic side effects, headache being the most common one. Treatment in the very beginning should start with a partial dose (half a pill) at bedtime with a small amount of food. Low incidence of side effects and its weekly dose has made Cabergoline a choice drug for treatment of related diseases.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Reproductive Problem
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
88 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Clomiphene citrate plus cabergoline
Arm Type
Active Comparator
Arm Description
This group will receive Clomiphene citrate 50 mg tablet twice daily from the second day of menses to the sixth day plus cabergoline 0.25 mg from second day every 3 days (4 doses only)
Arm Title
Clomiphene citrate plus placebo
Arm Type
Active Comparator
Arm Description
This group will receive Clomiphene citrate 50 mg tablet twice daily from the second day of menses to the sixth day plus placebo tablets from second day every 3 days (4 doses only)
Intervention Type
Drug
Intervention Name(s)
Clomiphene citrate
Intervention Description
50 mg tablet twice daily from the second day of menses to the sixth day
Intervention Type
Drug
Intervention Name(s)
Cabergoline
Intervention Description
Cabergoline 0.25 mg (half tablet) every 3 days (4 doses).
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
placebo(half tablet) every 3 days (4 doses).
Primary Outcome Measure Information:
Title
Size of mature follicles (mm).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Number of pregnancy
Time Frame
1 year
Title
Number of mature follicles (mm)
Time Frame
1 year
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
2 or more of PCOS signs according to Rotterdam diagnostic criteria (2003).-
Primary or secondary infertility.-
Absence of galactorrhoea
Normal serum prolactin or slightly elevated (up to 50 ng/dl)
Normal hysterosalpingography
Normal spermogram
Exclusion Criteria:
Women on other line of treatment as aromatase inhibitors, gonadotrophins, or tamoxifen.
Known hypersensitivity for Clomiphene citrate or cabergoline.
Other factors of infertility as tubal factor, uterine factor or male factor.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kamal M Zahran, MD
Phone
+20882414616
Email
drzahranmk@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mohammed K Ali, MD
Phone
+20882414621
Email
m_khairy2001@yahoo.com
Facility Information:
Facility Name
Assiut university
City
Assiut
ZIP/Postal Code
71111
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kamal M Zahran, MD
12. IPD Sharing Statement
Learn more about this trial
Clomiphene Citrate Plus Cabergoline in Treatment of Polycystic Ovary Syndrome
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