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Comparison of standard dose protocol with extended dose protocol of letrozole for ovulation induction in women with PCOS

Comparison of standard dose protocol with extended dose protocol of letrozole for ovulation induction in women with PCOS

Status
Unknown
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250811004
Enrollment
174
Registered
2025-08-11
Start date
2025-03-28
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

polycystic ovaries reproductive age females with anovulation PCOS anovulation letrozole

Interventions

Letrozole given for 5 days for ovulation induction in female with subfertility.,Letrozole given for 10 days for ovulation induction in female with subfertility.
Active Comparator Drug,Active Comparator Drug
Letrozole short course,Letrozole long course

Sponsors

fatima jinnah medical university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Women of 18-35 years of age. 2. Diagnosed case of PCOS on TVS. 3. Subfertility for one year or more.

Exclusion criteria

Exclusion criteria: 1. .Patients with evidence of tubal blockage on HSG/laparoscopy. 2. Patients whose husband has abnormal semen analysis 3. Patients with benign ovarian/uterine tumors. 4. Patients having other coexistent cause of infertility like endometriosis or fibroid 5. Patients with uncontrolled metabolic or endocrinological disorder

Design outcomes

Primary

MeasureTime frame
follicle development day 12 of cycle USG measurement of follicle on day 12

Secondary

MeasureTime frame
Clinically proven pregnancy at the end of cycle/missed period Serum beta HCG

Countries

Pakistan

Contacts

Public ContactRizwana Tariq

Fatima Jinnah Medical University

rizwanatariq@hotmail.com923236464820

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026