The Effect of Sildenafil Citrate on the Success Rate of Ovulation Induction Using Clomiphene
Primary Purpose
Anovulatory
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Sildenafil & clomiphene citrate
clomiphene only
Sponsored by
About this trial
This is an interventional treatment trial for Anovulatory
Eligibility Criteria
Inclusion Criteria:
- Women age 21-35 years.
- Anovulatory cycles due to polycystic ovaries syndrome.
- Non-smokers.
- Free of major medical illness
Exclusion Criteria:
- Women with myoma or adenomyosis
- Women with congenital uterine anomaly.
- Chronic use of any medications including non-steroidal anti-inflammatory drugs.
- Associated cases of infertility other than PCOs (male factor, tubal factor,….).
- Asherman syndrome.
- Cases with endometrial hyperplasia.
- Cases with endometrial polyp
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
(Sildenafil & clomiphene citrate group)
clomiphene only
Arm Description
105 Patients will receive 25 mg sildenafil citrate 6 hourly orally (day 6 to the end of the cycle), and clomiphene citrate 100 mg/day (day 2 to 6) orally by the patient, for induction of ovulation
105 patients will receive only clomiphene citrate 100mg/day (day 2 to 6) orally (2 tablets at same time daily).
Outcomes
Primary Outcome Measures
Clinical pregnancy rate
Secondary Outcome Measures
endometrial thickness
miscarriage rate
ectopic pregnancy rate
Side Effects of Vasodilators
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02663830
Brief Title
The Effect of Sildenafil Citrate on the Success Rate of Ovulation Induction Using Clomiphene
Official Title
The Effect of Sildenafil Citrate on the Success Rate of Ovulation Induction Using Clomiphene: A Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
January 10, 2016 (Actual)
Primary Completion Date
January 10, 2017 (Actual)
Study Completion Date
March 12, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the study is to evaluate the effect of sildenafil citrate on the pregnancy rate in women undergoing induction of ovulation using clomiphene citrate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anovulatory
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
210 (Actual)
8. Arms, Groups, and Interventions
Arm Title
(Sildenafil & clomiphene citrate group)
Arm Type
Experimental
Arm Description
105 Patients will receive 25 mg sildenafil citrate 6 hourly orally (day 6 to the end of the cycle), and clomiphene citrate 100 mg/day (day 2 to 6) orally by the patient, for induction of ovulation
Arm Title
clomiphene only
Arm Type
Active Comparator
Arm Description
105 patients will receive only clomiphene citrate 100mg/day (day 2 to 6) orally (2 tablets at same time daily).
Intervention Type
Drug
Intervention Name(s)
Sildenafil & clomiphene citrate
Other Intervention Name(s)
seldin and clomid
Intervention Description
105 Patients will receive 25 mg sildenafil citrate 6hourly orally (day 6 to the end of the cycle), and clomiphene citrate 100 mg/day (day 2 to 6) orally by the patient, for induction of ovulation
Intervention Type
Drug
Intervention Name(s)
clomiphene only
Other Intervention Name(s)
clomid
Intervention Description
105 Patients will receive clomiphene citrate 100 mg/day (day 2 to 6) orally by the patient, for induction of ovulation
Primary Outcome Measure Information:
Title
Clinical pregnancy rate
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
endometrial thickness
Time Frame
2 weeks
Title
miscarriage rate
Time Frame
13 weeks
Title
ectopic pregnancy rate
Time Frame
8 weeks
Title
Side Effects of Vasodilators
Time Frame
4 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women age 21-35 years.
Anovulatory cycles due to polycystic ovaries syndrome.
Non-smokers.
Free of major medical illness
Exclusion Criteria:
Women with myoma or adenomyosis
Women with congenital uterine anomaly.
Chronic use of any medications including non-steroidal anti-inflammatory drugs.
Associated cases of infertility other than PCOs (male factor, tubal factor,….).
Asherman syndrome.
Cases with endometrial hyperplasia.
Cases with endometrial polyp
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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The Effect of Sildenafil Citrate on the Success Rate of Ovulation Induction Using Clomiphene
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