Overview
Effect of Metformin on Non PCO Women Undergoing IVF/ICSI
Status:
Recruiting
Recruiting
Trial end date:
2020-11-27
2020-11-27
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
400 Patients will be randomly assigned into two groups after informed consent from every patient. They will be classified into 2 groups: Group A ( involves 200 patients ) will receive metformin 850 mg twice daily along the cycle of Intra-cytoplasmic sperm injection (ICSI) Group B ( involve 200 patients) will not receive metformin. They will undergo a cycle of ICSI. Primary outcome of this trial is to detect occurrence of Ovarian Hyper-stimulation Syndrome (OHSS) , while secondary outcomes include quality & number of retrieved follicles fertilization rate ,ongoing pregnancy rate & endometrial thickness.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Kasr El Aini HospitalTreatments:
Metformin
Criteria
Inclusion Criteria:- Patients subjected to IVF/ICSI aged 20-35 years with long agonist protocol
- history of infertility for at least two years (either primary or secondary)
- normal TSH and prolactin
Exclusion Criteria:
- Patients who used metformin in the past 3-months before study
- having medical problems such as kidney or liver diseases
- Severe endometriosis.
- hypothalamic amenorrhea.
- Severe male factor( patients with testicular biopsy or those with azoospermia).
- Associated uterine factor.
- IVF/ ICSI for sex selection.