The Evaluation of The Effects 2 protocols in pregnancy
Not Applicable
- Conditions
- infertility.Female Infertility
- Registration Number
- IRCT2014050516858N3
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 137
Inclusion Criteria
inclusion criteria: female patient age 18–35 years; presence of a regular ; proven ovulatory menstruation cycle with a length of 26–35 days, more that 5 million sperm in SA(semen analysis);body mass index (BMI) of 18–30 kg/m ; ?rst ICSI attempt . Exclusion criteria:established systemic disease ;ovary and Uterus abnormalities;repeated abortions
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase Endometrial Thickness. Timepoint: 2 Days After HCG Injection. Method of measurement: Sonography.;Increase Implantation. Timepoint: 3 weeks. Method of measurement: Lab Test.;Increase Clinical Pregnancy. Timepoint: 3 weeks. Method of measurement: Sonography.;Decrease Treatment Cost. Timepoint: Delivery Time. Method of measurement: Counting-RIALs.;Estradiol. Timepoint: Beginning time of study. Method of measurement: Lab Test.;LH. Timepoint: first and 4th week of study. Method of measurement: Lab Test.;FSH. Timepoint: first and 4th week of study. Method of measurement: Lab Test.;Chemical pregnancy. Timepoint: End of study. Method of measurement: Lab Test.
- Secondary Outcome Measures
Name Time Method Increase follicular number. Timepoint: 8 days. Method of measurement: 8days.;Embryo transfer. Timepoint: delivery time. Method of measurement: fertility rate.