MedPath

Effect of luteal phase stimulation with follicular phase stimulation in poor ovarian response

Phase 3
Conditions
Poor ovarian response.
Ovarian dysfunction
Registration Number
IRCT20210405050852N1
Lead Sponsor
Avicenna University Jihad Infertility Center Avicenna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
78
Inclusion Criteria

History of an ovulation stimulation cycle with less than 4 oocytes
AMH<1.1 ng/ml or AFC<5
The total number of motile sperm is at least 15 million
Normal uterus in ultrasound and hysterosalpingography
Regular periods of 21-35 days
Indication for IVF
Ability to participate and collaborate with study protocol
Signature informed consent
Under 40 years

Exclusion Criteria

History of ovarian surgery
History of pelvic cytotoxic radiation exposure due to malignancy
History of recurrent miscarriage
Grade III or IV endometriosis
Concomitant uterine pathology (adenomyosis, submucosal myoma, Asherman syndrome)
Autoimmune disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of metaphase II oocyte. Timepoint: End of ovarian stimulation. Method of measurement: Observation of metaphase 2 oocytes extracted by the embryologist.
Secondary Outcome Measures
NameTimeMethod
Chemical pregnancy rate. Timepoint: 14 days after transfer. Method of measurement: Beta-Human Chorionic Gonadotropin.;Clinical pregnancy. Timepoint: Pregnancy 7th weeks. Method of measurement: Detect of fetal heart beat on ultrasound.;Total number of embryos. Timepoint: After in vitro fertilization. Method of measurement: 18-20 hours after in vitro fertilization.
© Copyright 2025. All Rights Reserved by MedPath