A Randomised Trial Using Highly Purified Human Chorionic Gonadotropin (HP-hCG) and Recombinant Human Chorionic Gonadotropin (rhCG) in Women Undergoing Controlled Ovarian Stimulation
- Conditions
- Infertility
- Interventions
- Drug: highly purified human chorionic gonadotropin
- Registration Number
- NCT02449889
- Lead Sponsor
- Ferring Pharmaceuticals
- Brief Summary
This trial is investigating the efficacy and safety of highly purified human chorionic gonadotropin (HP-hCG) and recombinant human chorionic gonadotropin (rhCG) for triggering of final follicular maturation in women undergoing controlled ovarian stimulation
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 176
- Pre-menopausal females between the ages of 18 and 39 years
- Documented history of infertility
- Body mass index (BMI) between 17.5 and 32.0 kg/m2
- Regular menstrual cycles
- Known endometriosis stage III and IV
- Known polycystic ovarian syndrome (PCOS)
- History of recurrent miscarriage
- History of more than three previous controlled ovarian stimulation cycles
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description rhCG recombinant human chorionic gonadotropin recombinant human chorionic gonadotropin HP-hCG IM highly purified human chorionic gonadotropin highly purified human chorionic gonadotropin, intramuscularly (IM) HP-hCG SC highly purified human chorionic gonadotropin highly purified human chorionic gonadotropin, subcutaneously (SC)
- Primary Outcome Measures
Name Time Method Number of Oocytes Retrieved Approximately 36 hours after hCG administration Oocyte retrieval took place 36 h (±2h) after hCG administration. At oocyte retrieval the number of oocytes retrieved was recorded.
- Secondary Outcome Measures
Name Time Method Frequency of Adverse Events (AEs) AEs were collected from signing informed consent until end of trial visit = maximum period approximately 5 months. However, only TEAEs are presented The number of treatment-emergent AEs (TEAEs) in each treatment group will be presented.
Number of Metaphase II (MII) Oocytes Prior to insemination (within 6 hours after oocyte retrieval) Only applicable for insemination using intracytoplasmic sperm injection (ICSI). The MII oocytes were counted prior to insemination.
Intensity of AEs AEs were collected from signing informed consent until end of trial visit = maximum period approximately 5 months. However, only TEAEs are presented. The intensity of an TEAE would be classified using the following 3-point scale: mild (awareness of signs or symptoms, but no disruption of usual activity), moderate (event sufficient to affect usual activity \[disturbing\]) or severe (inability to work or perform usual activities \[unacceptable\]).
Number of Fertilized (2 Pronuclei (2PN)) Oocytes One day after oocyte retrieval Fertilization was assessed by counting the number of pronuclei, which was recorded as 0, 1, 2 or \>2. Correct fertilization was defined as oocytes with 2PN.
Positive β Unit of Human Chorionic Gonadotropin (βhCG) Rate 13-15 days after transfer Defined as percentage of subjects with positive beta hCG. A positive β hCG was confirmed by a blood test obtained 13-15 days after transfer.
Clinical Pregnancy Rate 5-6 weeks after transfer Defined as percentage of subjects with clinical pregnancy. Clinical pregnancy was defined as at least one gestational sac 5-6 weeks after transfer.
Trial Locations
- Locations (1)
Instituto Ideia Fértil de Saúde Reproductive (there may be other sites in this country)
🇧🇷São Paulo, Brazil