Desogestrel (DSG) and Corifollitropin(FSH-CTP) Alfa for Ovarian Stimulation in Donors

Sponsor
Institut Universitari Dexeus (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02757287
Collaborator
Fundación Dexeus Salud de la Mujer (Other)
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Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
  • Drug: FSH-CTP + DESOGESTREL
Phase 4

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

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Desogestrel and Corifollitropin Treatment for Ovarian Stimulation in Donors
Actual Study Start Date :
May 1, 2016
Actual Primary Completion Date :
Nov 1, 2017
Anticipated Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: FSH-CTP + DESOGESTREL

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

Drug: FSH-CTP + DESOGESTREL
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

Outcome Measures

Primary Outcome Measures

  1. Total dose of gonadotrophins [At the end of the stimulation treatment period (5 or 7 days after begining of treatment)]

    Total Consume of gonadotrophins

Secondary Outcome Measures

  1. Plasma LH [Day of GnrH bolus]

    Level of LH in plasma (mIU/ml)

  2. Number of mature oocytes [Day of oocyte recovery]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Quiron Dexeus Barcelona Spain 08028

Sponsors and Collaborators

  • Institut Universitari Dexeus
  • Fundación Dexeus Salud de la Mujer

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Dr. Francisca Martínez, PhD, Institut Universitari Dexeus
ClinicalTrials.gov Identifier:
NCT02757287
Other Study ID Numbers:
  • SMD-DES-2016-01
First Posted:
May 2, 2016
Last Update Posted:
Sep 5, 2018
Last Verified:
Sep 1, 2018
Keywords provided by Dr. Francisca Martínez, PhD, Institut Universitari Dexeus
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 5, 2018