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letrozole combined with gonadotropin in infertile patients with diminished ovarian reserve

Ovarian response to letrozole combined with gonadotropin regimen in patient with diminished ovarian reserve candidate for IVF

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140224016705N9
Enrollment
72
Registered
2019-12-18
Start date
2017-03-21
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

infertility. Female infertility associated with anovulation

Interventions

Intervention group: The patient were treated by letrozole at 7.5 mg/day (Saha pharmaceutical company) and Gonal-f at 225 mg/day (Merck pharmaceutical company), started on the 2nd-3rd day of menstrual

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 42 Years

Inclusion criteria

Inclusion criteria: women with poor ovarian response that at least two of the following three features(Bologna criteria) must be present: (i) advanced maternal age or any other risk factor for POR; (ii) a previousPOR; and (iii) an abnormal ovarian reserve test. age 18-42 years previous poor ovarian response(oocyte<3) to ovarian stimulation by gonadotropin.

Exclusion criteria

Exclusion criteria: metabolic disease (diabetes, chronic hypertension, etc) or any underlying disease ( kidney disease, liver disease, etc.) presence cancer or any malignancy genitourinary anomalies

Design outcomes

Primary

MeasureTime frame
Number of oocytes achieved after letrozole+gonadotropine regimen. Timepoint: after ovarian puncture. Method of measurement: reporting by embryology laboratory.;Mean endometrial thickening after letrozole+gonadotropin regimen. Timepoint: at injection day of HCG. Method of measurement: ultrasound sonography.;Rate of pregnancy after letrozole+gonadotropin regimen. Timepoint: 2weeks after ovarian puncture. Method of measurement: level of beta human chorionic gonadotropin in a sample of blood.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNegar Hamzehpour

Shahid Beheshti University of Medical Sciences

dr.n.hamzehpour@gmail.com+98 21 5506 2628

Outcome results

None listed

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