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Sildenafil Effect After Ovulation Induction

Effect of Sildenafil Citrate on Pregnancy Rate in Women Undergoing Induction of Ovulation

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02890238
Enrollment
100
Registered
2016-09-07
Start date
2016-08-31
Completion date
2019-12-31
Last updated
2019-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Keywords

Sildenafil Citrate, Induction of Ovulation, Pregnancy Rate

Brief summary

100 women with infertility classified into 2 groups. Group A: Included 50 women who will be given clomiphene citrate 50mg (clomid) orally 2 times/day from 2rd-7th day of the cycle and sildeaynafil citrate 20mg tab from 7th-11th day of the same cycle orally 3 times/day. Group B: Included 50 women who will be given clomiphene citrate 50mg (clomid) orally 2 times/day from 2rd-7th day of the cycle and placebo tablets from 7th-11th day of the same cycle orally 3 times/day.

Detailed description

100 women with infertility classified into 2 groups. Group A: Included 50 women who will be given clomiphene citrate 50mg (clomid) orally 2 times/day from 2rd-7th day of the cycle and sildeaynafil citrate 20mg tab from 7th-11th day of the same cycle orally 3 times/day. Group B: Included 50 women who will be given clomiphene citrate 50mg (clomid) orally 2 times/day from 2rd-7th day of the cycle and placebo tablets from 7th-11th day of the same cycle orally 3 times/day. Folliculometry was assessed by: * Transvaginal ultrasound: It was done on day 11th of the cycle to detect number of follicles and endometrial thickness. When the follicles reach ≥18 ml, injection of 5000 IU of HCG IM to trigger ovulation to both groups. Pregnancy was assessed by: * Beta HCG test: (Radioimmunoassay)

Interventions

DRUGClomiphene citrate

50mg (clomid,) orally 2 times/day from 2nd- 7th day of the cycle

DRUGsildenafil citrate

20mg tab from 7th-11th day of the same cycle orally 3times/day

DRUGPlacebo

tab from 7th-11th day of the same cycle orally 3times/day

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Infertile women whether it's primary or secondary infertility 2. Woman's age: (18-35 years old) 3. Menstrual cycle from (24-35 days) 4. Normal semen analysis

Exclusion criteria

1. Age more than 35 years old 2. Ovarian cysts 3. Abnormal hormonal profile (e.g hyperprolactinaemia) 4. Significant cardiovascular disease 5. Serious liver disease or renal failure 6. Poorly controlled diabetes mellitus

Design outcomes

Primary

MeasureTime frameDescription
Pregnancy rate per cycle14 days after HCG triggering of ovulationSerum pregnancy test

Countries

Egypt

Contacts

Primary ContactAhmed Maged
prof.ahmedmaged@gmail.com01005227404

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026