Evaluation of the outcome of ART in dual trigger method compared to the usual method in poor responder patients
Not Applicable
Recruiting
- Conditions
- Infertility in poor responder patients.Female infertility
- Registration Number
- IRCT20220409054458N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
All poor responder patients according to BOLOGNIA criteria who are ART candidates and are in GnRH Antagonist cycle.
Exclusion Criteria
Grade 3 and 4 endometriosis
Hydrosalpinx
Endocrine disorders such as hyperprolactinemia, thyroid and adrenal problems
Azoospermia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The number of oocytes obtained in the ovulation stimulation cycle. Timepoint: Number of oocytes obtained after ovarian puncture in the ovulation stimulation cycle. Method of measurement: Count the number of oocytes obtained per cycle.
- Secondary Outcome Measures
Name Time Method Chemical pregnancy rate. Timepoint: 2 weeks after oocyte transfer into the uterus. Method of measurement: Serum BHCG level.;Clinical pregnancy rate. Timepoint: 5 weeks after oocyte transfer into the uterus. Method of measurement: Vaginal ultrasound examination of the pregnancy sac.