Antral Follicle Priming Prior to ICSI (Intracytoplasmic Sperm Injection) in Previously Diagnosed Low Responders (FOLLPRIM)
Ovarian Diseases
About this trial
This is an interventional treatment trial for Ovarian Diseases focused on measuring estradiol, testosterone, combined oral contraceptive, low responders, ICSI
Eligibility Criteria
Inclusion Criteria:
Phase 1 (Non randomized. The patient must fit the first plus at least other 2 criteria)
- Infertility requiring an IVF/ICSI treatment
- Age ≥ 38 years
- Basal FSH ≥ 10 mUI/ml (day 3 of the cycle)
- Serum AMH ≤ 5 pmol/l
- Antral follicular count ≤ 6 (day 3 of the cycle)
Phase 2 (Randomized. The patient must fit at least one criterion regarding the day of GNRH analogue administration during the cycle performed in Phase 1)
- Less than 4 follicles which mean diameter measuring more than 16mm
- Serum estradiol levels ≤ 500 pg/ml
- 4 MII or less than 4 MII oocytes retrieved
Exclusion Criteria:
- Patients suffering of endometriosis
- Patients having progesterone levels ≤ 4 ng/ml (day 21 of the cycle)
- Patients having a partner affected by severe oligo/astheno/teratozoospermia
Sites / Locations
- La Fe University Hospital. Department of Obstetrics and Gynecology
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
Testosterone
Estradiol
CombEq
Transdermal testosterone (20µg/day) from day 24 of the previous cycle until day 2 of the ICSI cycle
Transdermal estradiol (200µg/day)from day 20 of the previous cycle to day 3 of the ICSI cycle
(150µg Desogestrel + 30µg Ethinylestradiol)/day during the luteal phase of the two cycles prior to the ICSI Estradiol valerate 4 mg/day during 10 days, starting the second day of the cycle prior to the ICSI cycle.