Status:
COMPLETED
Endometrial Receptivity After GnRH Agonist Triggering
Lead Sponsor:
IVI Madrid
Conditions:
Ovarian Hyperstimulation Syndrome
Eligibility:
FEMALE
18-35 years
Phase:
PHASE4
Brief Summary
Conventional luteal phase support after human chorionic gonadotrophin (hCG) triggering in women undergoing in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) provides adequate pregnanc...
Eligibility Criteria
Inclusion
- Inclusion criteria :
- Healthy oocyte donor women
- Aged 18-35 years
- With a menstrual cycle length of 26-35 days
- Normal ultrasound scan of uterus and ovaries
- Normal basal hormones
- No contraindication for controlled ovarian stimulation (COS)
- Willing to participate in the study and providing written informed consent.
- Exclusion Criteria:
- Subjects with current or previous history of an endocrine abnormality
- Subjects with an abnormal outcome of blood biochemistry or hematology
- Subjects with an abnormal cervical smear
- Subjects with a chronic disease
- Subjects with any relevant ovarian-, tubal- or uterine-pathology that could interfere with the COS treatment
- Pregnancy
- Subjects who had a previous history of ovarian hyperresponse or ovarian hyperstimulation syndrome (OHSS), polycystic ovary syndrome (PCOS) or a basal antral follicle count (AFC) of more than 20 on ultrasound (11 mm, both ovaries combined) .
- Previous low ovarian response to FSH or hMG treatment (i.e. cycle cancelled due to insufficient ovarian response or less than 6 oocytes obtained).
- A history of recurrent miscarriage,
- Smoking more than 10 cigarettes per day.
- Not willing to comply with study procedures
Exclusion
Key Trial Info
Start Date :
November 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
35 Patients enrolled
Trial Details
Trial ID
NCT01500863
Start Date
November 1 2011
Last Update
October 26 2016
Active Locations (1)
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1
Instituto Valenciano de Infertilidad
Madrid, Madrid, Spain, 28035