Comparison of two protocols for controlled ovarian stimulation in infertile women undergoing assisted reproductive technology

Phase 2

• Conditions: Female infertility; Infertility.

• Registration Number: IRCT201107286420N5
• Lead Sponsor: Deputy of Research and Technology, Yazd Shahid Sadoughi Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 April 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 130

Inclusion Criteria

Age<38 years
Regular menstrual cycle (25-35 days)
BMI <30 kg/m 2
Normal uterus and ovaries in vaginal ultrasound
FSH<10IU/

Exclusion Criteria

Severe endometriosis
Polycystic ovarian syndrome
History of pelvic surgery
Azoospermia
More than two IVF or ICSI cycle failures

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Chemical pregnancy. Timepoint: 2 weeks. Method of measurement: BHCG serum.

Secondary Outcome Measures

Name	Time	Method
Clinical pregnancy. Timepoint: 7 weeks after embryo transfer. Method of measurement: Sonography.