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Clinical Trials/NCT02757287
NCT02757287
Withdrawn
Phase 4

Desogestrel and Corifollitropin Treatment for Ovarian Stimulation in Donors

Institut Universitari Dexeus1 site in 1 countryMay 2016

Overview

Phase
Phase 4
Intervention
FSH-CTP + DESOGESTREL
Conditions
Infertility
Sponsor
Institut Universitari Dexeus
Locations
1
Primary Endpoint
Total dose of gonadotrophins
Status
Withdrawn
Last Updated
7 years ago

Overview

Brief Summary

Currently, controlled ovarian stimulation (COS) in oocyte donors is performed by daily injections of gonadotropins( recombinant FSH) plus a GnRH Antagonist usually form 5th-6th stimulation day until ovulation induction with a bolus of another injection of a gonadotropin-releasing hormone (GnRH) Agonist. Injections of the GnRH Antagonist avoid untimely luteinizing hormone (LH) surge and spontaneous ovulation prior to follicular aspiration. There is a preparation of long-acting recombinant follicle stimulating hormone (rFSH= (corifollitropin alfa (FSH-CTP), Elonva®, MSD), that allows that a single subcutaneous injection substitutes the first 7 days of daily gonadotropin injections. On the other hand, a contraceptive oral progesterone only( Desogestrel, DSG) is available for contraception, avoiding the LH surge. It has been described the usefulness of orally administered medroxyprogesterone acetate, 10 mg to inhibit the endogenous LH surge in IVF patients during COS.

In donors, by administering a single injection of FSH-CTP and oral desogestrel since the first menstruation day, the total number of injections administered is reduced and less discomfort is experienced without adverse impact on ovarian response. No description of the hormonal and ovarian response under this protocol has been published

Detailed Description

* oral desogestrel since the first menstruation day, * a single injection of FSH-CTP on the 7th menstrual cycle day * routine monitoring of ovarian response with transvaginal ultrasound every second day until pre-ovulatory bolus of GnRH * Hormones measured on day of 7th menstrual cycle day , day of pre-ovulatory bolus of GnRH and the day after the bolus ( estradiol, FSH, Progesterone, LH) * Quality of Life questionnaire the day after the bolus

Registry
clinicaltrials.gov
Start Date
May 2016
End Date
December 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Institut Universitari Dexeus
Responsible Party
Principal Investigator
Principal Investigator

Dr. Francisca Martínez

PhD

Institut Universitari Dexeus

Eligibility Criteria

Inclusion Criteria

  • Population: donors (18-35 ) from candidates of Donor program
  • Fulfilling inclusión medical and legal criteria (RD -Ley de transposición de la normativa europea a la legislación española 9/2014)
  • Who had had undergone previously convencional COS (controlled ovarian stimulation) with FSH-CTP and daily antagonist injections
  • Given signed consent form.

Exclusion Criteria

  • Previous low response to COS
  • Previous ovarian hyperstimulation syndrome.
  • Ovarian cysts.

Arms & Interventions

FSH-CTP + DESOGESTREL

Single injection of FSH-CTP and oral desogestrel since the first menstruation day, until bolus of GnRH agonist to follicular maturation

Intervention: FSH-CTP + DESOGESTREL

Outcomes

Primary Outcomes

Total dose of gonadotrophins

Time Frame: At the end of the stimulation treatment period (5 or 7 days after begining of treatment)

Total Consume of gonadotrophins

Secondary Outcomes

  • Number of mature oocytes(Day of oocyte recovery)
  • Plasma LH(Day of GnrH bolus)

Study Sites (1)

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