The effect of dydrogesterone and various forms of progesterone in support of artificial reproduction techniques
Phase 2
- Conditions
- Artificial fertilization.Complications of attempted introduction of fertilized ovum following in vitro fertilization
- Registration Number
- IRCT2016010825902N1
- Lead Sponsor
- Vice chancellor For Research Of Ahvaz Jundishapur University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 159
Inclusion Criteria
Inclusion Criteria: Patients candidate for in vitro fertilization (IVF) or intracytoplasmic cytoplasmic sperm injection (ICSI); Having a normal uterus.
Exclusion Criteria
Abnormal uterus such as submucosal myoma and endometrial adhesions; Sensitivity to progesterone; Lack of fertilization; Having a systemic disease.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pregnancy. Timepoint: Once a week after embryo transfer into the patient. Method of measurement: The blood hCG test.;Preterm delivery. Timepoint: Every two weeks from the twentieth week of pregnancy. Method of measurement: Patient appointments and record uterine contractions.;Amount of live birth. Timepoint: Every two weeks from twenty-eighth week of pregnancy. Method of measurement: Patient appointments and record baby's birth.;Grade and the number of transferred embryo cells. Timepoint: Immediately before embryo transfer into the patient. Method of measurement: By using microscope.
- Secondary Outcome Measures
Name Time Method Perineal irritation caused by progesterone vaginal suppository. Timepoint: Every two weeks during treatment period. Method of measurement: Verbal questionnaire and the patient's response.