A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg Daily Versus Intravaginal Micronized Progesterone Capsules 600 mg Daily for Luteal Support in In-Vitro Fertilization
- Conditions
- Female Infertility
- Interventions
- Drug: Micronized Progesterone 600 mg
- Registration Number
- NCT01850030
- Lead Sponsor
- Abbott
- Brief Summary
Female inability to conceive a child. The purpose of this randomized, two-arm and double blind, double dummy study is to demonstrate that the treatment of a daily dose of 3x10mg dydrogesterone orally is as effective and safe as the daily dose of 3x200 mg micronized progesterone capsules administered intravaginally for the luteal support in patients undergoing IVF. The treatment will start on the day of oocyte retrieval and continue until pregnancy is negative or until week 12 gestation.Patients will be followed after treatment until 30 days after delivery to record any safety and tolerability data of the patient and their newborn(s).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 1070
- Signed informed consent
- Premenopausal females, age > 18 years < 42 years
- Non-smokers. For females who were past smokers, they must have stopped tobacco usage for at least 3 months prior baseline visit
- Early follicular phase (Day 2-4) Follicle stimulating hormone (FSH) less than or equal to 15 IU/L and estradiol (E2)within normal limits
- Luteinizing hormone (LH), prolactin (PRL), T (testosterone) and thyroid-stimulating hormone (TSH), within the normal limits for the clinical laboratory, or considered not clinically significant by the Investigator within 6 months prior to screening
- Documented history of infertility (e.g., unable to conceive for at least one year or for 6 months for women ≥ 38 years of age or bilateral tubal occlusion or absence)
- Normal transvaginal ultrasound at screening (or within 14 days of screening) without evidence of clinically significant abnormality consistent with finding adequate for Assisted Reproductive Technology (ART) with respect to uterus and adnexa (no hydrosalpinx or clinically relevant uterine fibroids)
- Negative pregnancy test on the day of pituitary down regulation (prior to administration of gonadotropin releasing hormones (GnRH) agonist or GnRH antagonist)
- Clinically indicated protocol for induction of IVF with a fresh embryo
- Single or dual embryo transfer
- BMI ≥ 18 and ≤ 30 kg/m2
- Evidence of cardiovascular, respiratory, urogenital, gastrointestinal/hepatic, hematologic/immunologic, head, ears, eyes, nose, throat (HEENT), dermatologic/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurologic/psychiatric, allergy, recent major surgery (< 3 months), or other relevant diseases as revealed by history, physical examination and/or laboratory assessments which could limit participation in or completion of the study
- Acute urogenital disease
- Known allergic reactions to progesterone products
- Known allergic reactions to peanuts and peanut oil
- Intake of experimental drug or participation in any other clinical trial within 30 days prior to study start
- Mental disability or any other lack of fitness, in the Investigator's opinion, to preclude subjects to participate in or to complete the study
- Current or recent substance abuse, including alcohol and tobacco (Note: Patients who stopped tobacco usage at least 3 months prior to screening visit would be allowed)
- History of chemotherapy or radiotherapy
- Patients with more than 3 unsuccessful IVF attempts
- Contraindication for pregnancy
- Refusal or inability to comply with the requirements of the study protocol for any reason, including scheduled clinic visits and laboratory tests
- History of recurrent pregnancy loss defined as 3 or more spontaneous miscarriages
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Dydrogesterone 30 mg Dydrogesterone 30 mg - Dydrogesterone 30 mg Placebo progesterone - Micronized Progesterone 600 mg Micronized Progesterone 600 mg - Micronized Progesterone 600 mg Placebo dydrogesterone -
- Primary Outcome Measures
Name Time Method Percentage of Participants Being Pregnant as Measured by the Presence of Fetal Heart Beats at 12 Weeks´Gestation Using Transvaginal Ultrasound 12 weeks´ gestation (at visit 6) Percentage of participants being pregnant as measured by the presence of fetal heart beats at 12 weeks´gestation using transvaginal ultrasound
- Secondary Outcome Measures
Name Time Method Percentage of Participants Being Pregnant as Measured by the Positive Biochemical Pregnancy Test on Day 14 After Embryo Transfer Day 14 after embryo transfer Percentage of participants being pregnant as measured by the positive biochemical pregnancy test on Day 14 after embryo transfer
Percentage of Participants With a Successful Completion of Pregnancy After delivery (about 9 months after IVF) Incidence of live births and healthy newborns
Gender of the Newborn After delivery (about 9 months after IVF) was recorded and collected for Newborn
Trial Locations
- Locations (39)
Site reference no. 113176
🇦🇹Vienna, Austria
Site reference no. 93615
🇧🇪Brussels, Belgium
Site reference no. 93597
🇧🇪Gent, Belgium
Center of Family Medicine LC
🇷🇺Ekaterinburg, Russian Federation
Site reference no. ORG-000637
🇪🇸Valencia, Spain
Site reference no. 93595
🇧🇪Leuven, Belgium
Site reference no. 93593
🇧🇪Brasschaat, Belgium
Site reference no. 93598
🇧🇪Brussels, Belgium
Site reference ID ORG-000642
🇩🇪Dresden, Germany
Site reference no. 93594
🇧🇪Gent, Belgium
Site reference no. 93616
🇧🇪Hasselt, Belgium
Site reference no. 93613
🇧🇪Genk, Belgium
Site reference no. ORG-000635
🇫🇮Oulu, Finland
Site reference ID ORG-000791
🇪🇸Barcelona, Spain
Site reference no. 93617
🇧🇪Brussels, Belgium
Moscow State Medical Dentistry University
🇷🇺Moscow, Russian Federation
Site reference no. 93614
🇧🇪Mons, Belgium
Site reference ID ORG-000884
🇫🇮Helsinki, Finland
Site reference ID ORG-000885
🇫🇮Jyväskylä, Finland
Site reference no. ORG-000633
🇫🇮Turku, Finland
Site reference ID ORG-000883
🇩🇪Luebeck, Germany
Site reference ID ORG-000645
🇩🇪Berlin, Germany
Site reference ID ORG-000643
🇩🇪Berlin, Germany
Site reference ID ORG-000644
🇩🇪Heidelberg, Germany
Site reference no. 93635
🇮🇱Be'er Sheva, Israel
Research facility ID ORG-000934
🇮🇱Hadera, Israel
Research facility ID ORG-000935
🇮🇱Haifa, Israel
Site reference no. 93638
🇮🇱Jerusalem, Israel
FGBU Endocrinology Research Center of Minzdrav of Russia
🇷🇺Moscow, Russian Federation
Site reference no. 93641
🇮🇱Tel Aviv, Israel
SBEIHPE - NWSMU n.a.l.l.Melnichko MoH and SD of RF
🇷🇺St. Petersburg, Russian Federation
CJSC "Nasledniki"
🇷🇺Moscow, Russian Federation
FSBI "Ural SRI of Maternity and Child Protection" of MoH and SD
🇷🇺Ekaterinburg, Russian Federation
St. Petersburg SBHI "Maternity Hospital No 17" (main address)
🇷🇺St. Petersburg, Russian Federation
Site reference no. 119915
🇪🇸Baracaldo, Vizcaya, Spain
Site reference no. ORG-000639
🇪🇸Bilbao, Spain
Site reference no. ORG-000638
🇪🇸Sevilla, Spain
Site reference no. ORG-000640
🇪🇸Pozuelo de Alarcon (Madrid), Spain
Site reference ID ORG-000795
🇫🇮Tampere, Finland