Fertility Clinical Trial
— 2-ShotOfficial title:
Comparison of Sequential CFA vs CFA +rFSH for Elective Fertility Preservation.. The 2-shot Protocol.
Verified date | December 2023 |
Source | Institut Universitari Dexeus |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This randomized was designed as non-inferiority trial aiming to compare the number of MII oocytes with 2-shot of Corifollitropin alpha (CFA) sequential administration: 150μg at stimulation day (SD) 1 and 100μg at SD 5 and 1-shot of CFA administration 150μg at SD 1 following by rFSH 200IU daily from SD 8 in women undergoing elective fertility preservation in a progestin-primed ovarian stimulation (PPOS) protocol and GnRH-agonist (GnRH-a) triggering.
Status | Recruiting |
Enrollment | 194 |
Est. completion date | January 2026 |
Est. primary completion date | September 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - AFC =20 - Anti-Mullerian hormone (AMH) =3ng/ml (AMH result of up to one year will be valid) - Between 18 and 40 years old - BMI >18 and <30 kg/m2 - Body weight > 50 kg for > 36 years - Able to come to the Center to comply with the procedures of the study: blood tests, appointments and drug dispensation. Exclusion Criteria: - Medically indicated fertility preservation - AFC > 20 - Polycystic ovarian syndrome (PCOS) according to the Rotterdam criteria - FSH = 20 - History of untreated autoimmune, endocrine or metabolic disorders - Contraindication for hormonal treatment - Recent history of severe disease requiring regular treatment (clinically significant concurrent medical condition that could compromise subject safety or interfered with the trial assessment). |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital Universitario Quiron Dexeus | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Fundación Santiago Dexeus Font | Organon |
Spain,
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Hwang JL, Chen SU, Chen HJ, Chen HF, Yang YS, Chang CH, Seow KM, Tzeng CR, Lin YH. Feasibility of corifollitropin alfa/GnRH antagonist protocol combined with GnRH agonist triggering and freeze-all strategy in polycystic ovary syndrome patients. J Formos Med Assoc. 2018 Jun;117(6):535-540. doi: 10.1016/j.jfma.2017.05.009. Epub 2017 Aug 19. — View Citation
La Marca A, Capuzzo M. Use of progestins to inhibit spontaneous ovulation during ovarian stimulation: the beginning of a new era? Reprod Biomed Online. 2019 Aug;39(2):321-331. doi: 10.1016/j.rbmo.2019.03.212. Epub 2019 Mar 29. — View Citation
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of MII oocytes retrieved | Number of MII oocytes retrieved | Trough study completion, an average of 10-20 days. | |
Secondary | Total number of oocytes retrieved | Total number of oocytes retrieved | Trough study completion, an average of 10-20 days. | |
Secondary | FSH | Endocrine profile FSH | Up to oocyte pickup, an average of 10-20 days. | |
Secondary | LH | Endocrine profile LH | Up to oocyte pickup, an average of 10-20 days. | |
Secondary | PROGESTERONE | Endocrine profile PROGESTERONE | Up to oocyte pickup, an average of 10-20 days. | |
Secondary | Estradiol | Endocrine profile Estradiol | Up to oocyte pickup, an average of 10-20 days. | |
Secondary | OHSS | Incidence of OHSS | Until 15 days after day of oocyte pick-up | |
Secondary | FertiQoL | Quality of life questionnaire "FertiQoL" | from stimulation day 1 until the day of oocyte pick-up,10-20 days after the beggining of the stimulation. | |
Secondary | Length of stimulation | Total days of stimulation | up to 18 days | |
Secondary | Adverse events | Frequency of adverse events | up to 20days |
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