Evaluation of the effect of uterine flushing with human chorionic gonadotropin (hCG) on biochemical and clinical pregnancy rate in the IUI cycle of couples with idiopathic infertility
Phase 3
Recruiting
- Conditions
- Female infertility.Female infertility, unspecifiedN97.9
- Registration Number
- IRCT20220702055335N1
- Lead Sponsor
- Vice chancellor for Research,Tabriz
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Having an informed consent to participate in the study
Unexplained infertility diagnosis
The health of the uterus structure
Normal sperm analysis
Women between 20 and 38 years old
The presence of ovulation
Exclusion Criteria
unsatisfaction for the participation of study
Moderate to severe endometriosis
hyper prolactinemia
Hyperthyroidism
Hypothyroidism
Ovarian Cysts
Kidney and liver failure
Blocked fallopian tubes
Increased FSH
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical pregnancy rate. Timepoint: 28 days after transfer. Method of measurement: vaginal sonography.;Chemical pregnancy rate. Timepoint: 14 days after transfer. Method of measurement: BhCG test.
- Secondary Outcome Measures
Name Time Method