Phase 2
Completed N=85
Exploratory Study Assessing Synchronisation of Egg Sacs With Degarelix
Infertility, Female
Source: ClinicalTrials.gov NCT00434122 ↗
Enrolled (actual)
85
Serious AEs
1.2%
Results posted
Apr 2009
Primary outcomePrimary: Coefficient of Variation of Follicular Sizes on Stimulation Day 1 (Follicles ≥ 2 mm) — 36.7; 39.2 Percentage
Summary
The main purpose of this clinical research study is to investigate if degarelix can synchronise the growth of the egg sacs in the ovaries and if degarelix has any effect on the lining of the womb.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Coefficient of Variation of Follicular Sizes on Stimulation Day 1 (Follicles ≥ 2 mm) |
36.7; 39.2 | — |
| SECONDARY Frequency of Oocyte Donors With Adequate Secretory Transformation at the Endometrial Histology Evaluation 7 Days After Injection With Human Chorionic Gonadotrophin (hCG) |
31; 11; 14 | — |
Eligibility Criteria
Inclusion Criteria
- Signed Informed Consent Form, prior to screening evaluations
- In good physical and mental health
- Pre-menopausal females between the ages of 18-35 years (both inclusive) at the time of randomisation
- Regular menstrual cycles of 26-35 days duration (both inclusive), presumed to be ovulatory
- Body mass index (BMI) between 18 and 29 kg/m2 (both inclusive)
- Willing to donate the retrieved oocytes
- Willing to use an adequate barrier method of contraception from informed consent to Day hCG injection +7 and to use an adequate barrier or hormonal method of contraception from Day hCG injection +7 to the end-of-study visit
Exclusion Criteria
- Abnormal karyotype
- Any known clinically significant systemic disease (e.g., insulin dependent diabetes)
- Any known endocrine or metabolic abnormalities (pituitary, adrenal, pancreas, liver or kidney) which can compromise participation in the study
- Diagnosed with polycystic ovarian syndrome or endometriosis stage III/IV
- Diagnosed as "poor responder"
- History of recurrent miscarriage (defined as three consecutive spontaneous losses before weeks 24 of pregnancy)
- Pregnancy or lactation
- Use of any investigational drug during 3 months prior to start of the current COH cycle
- Previous participation in the study
- Hypersensitivity to any trial product
Data sourced from ClinicalTrials.gov (NCT00434122). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.