Comparing the results of ovulation stimulationDouble or dual stimulation in poor ovarian responders

Not Applicable

Recruiting

• Conditions: Infertility.; Female infertility associated with anovulation; N97.0

• Registration Number: IRCT20130603013566N12
• Lead Sponsor: Vice chancellor for Research,Tabriz University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

The patients with first type of infertility
Age 20 to 42 years

Exclusion Criteria

Severe oligospermia
BMI is 30 or higher
Severe endometriosis
Concomitant chronic disease
Smoking and alcohol consumption

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
umber of resulted oocytes. Timepoint: The day of oocytes pick up. Method of measurement: Microscopic evaluation.;Quality of resulted oocytes. Timepoint: The day of oocytes pick up. Method of measurement: Microscopic evaluation.;Dosage of Follicle-stimulating hormone.(FSH). Timepoint: From day 2 until the time of injection. Method of measurement: Number of follicle stimulating (FSH) hormone ampoules.;Dosage of Generic human menopausal gonadotropin (hMG). Timepoint: From day 2 until the time of injection. Method of measurement: Number of Generic human menopausal gonadotropin (hMG).

Secondary Outcome Measures

Name	Time	Method
Implantation rate. Timepoint: 4-6 weeks after embryos transfer (ET). Method of measurement: Vaginal sonography.;Ongoing pregnancy rate. Timepoint: Pregnancy after 12 weeks of gestation. Method of measurement: Ultrasound.