Skip to content

The comparison of efficacy and outcomes of Triptorelin (Diphereline®) and hCG in ovulation trigger in infertile women with poly cystic ovarian syndrome

The comparison of efficacy and outcomes of Triptorelin (Diphereline®) and hCG in ovulation trigger in infertile women with poly cystic ovarian syndrome in IUI cycle: A randomize clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200122046221N3
Enrollment
120
Registered
2022-03-16
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Infertility in women with Poly cystic ovarian syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group: Give two Letrozole tablets (2.5 mg) from Abureyhan Pharmaceutical Company, daily for 5 days for 3-7 days during only one menstrual cycle and then trans vaginal ult

Sponsors

Jahrom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Infertile women who do not become pregnant one year after cohabitation and intercourse without the use of contraceptives From 15 years old to 45 years old With Poly cystic ovarian syndrome

Exclusion criteria

Exclusion criteria: Semen analysis and abnormal hysterosalpingography Over 45 years old Myoma Hyperprolactinemia Hypothyroidism Hyperthyroidism FSH> 12 Women with endometriosis History of contact with any substance induced by previous ovulation Kidney and liver disease Any contraindications to Diphereline and hCG Male factor

Design outcomes

Primary

MeasureTime frame
Pregnancy. Timepoint: End of menstrual cycle. Method of measurement: Serum b-hCG.

Secondary

MeasureTime frame
Incidence of ovarian hyperstimulation syndrome. Timepoint: End of menstrual cycle. Method of measurement: Clinical signs and ultrasound.;Incidence of multiple birth. Timepoint: End of menstrual cycle. Method of measurement: ultrasound sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAthar Rasekhjahromi

Jahrom University of Medical Sciences

A.rasekh@jums.ac.ir+98 71 5433 1521

Outcome results

None listed

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