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Evaluation of the effect of sildenafil and melatonin on fertility outcomes in women with poor ovarian response

Evaluation of the effect of sildenafil plus melatonin on fertility outcomes in infertile women with poor ovarian response undergoing assisted reproductive treatment.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160524028038N15
Enrollment
88
Registered
2023-01-14
Start date
2023-01-06
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Female infertility due to poor ovarian response. Female infertility of other origin

Interventions

Intervention 1: Intervention group A: Sildenafil (sildenafil citrate 25 mg daily
Visarsin) starting from the first day of the cycle until the day of egg retrieval) along with Inofolic (Inofolic powder 4 grams daily) starting from the first day of the previous cycle for 40 days. In
Razak Pharmaceutical Company, Iran) starting from the first day of the cycle until the day of egg retrieval along with inofolic (inofolic powder 4 grams daily) starting from the first day of the previ
Visarsin) starting from the first day of the cycle until the day of egg retrieval with inofolic (inofolic powder 4 grams daily) starting from the first day of the previous cycle for 40 days. Intervent

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 45 years Not using other vasodilator drugs such as nitric oxide and calcium channel blockers Normal semen analysis Poor ovarian response

Exclusion criteria

Exclusion criteria: Patients with other endocrine disorders such as hyperprolactinemia, PCOS, etc. History of ovarian surgery or ovarian endometrioma Smoker Cardiovascular disorders Unwillingness to cooperate Sildenafil sensitivity and intolerance to side effects (hot flashes, vision disorders, severe drop in blood pressure and hearing disorders)

Design outcomes

Primary

MeasureTime frame
Oocyte Quality. Timepoint: 2-3 hrs. after oocyte collection. Method of measurement: Microscopic Evaluation.;Number of retried oocyte. Timepoint: On day of oocyte retrieval. Method of measurement: Counting number of total oocytes with microscope.;Number of embryo. Timepoint: On the 2nd day after ICSI. Method of measurement: Observation with microscope.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Azizi

Bandare-abbas University of Medical Sciences

Maryamazizikut86@gmail.com+98 76 3333 0755

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026