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Conventional Ovarian Stimulation vs. Single Injection Stimulation of Corifollitropin Alfa in Oocyte Donor

Phase 4
Completed
Conditions
Ovarian Stimulation
Interventions
Drug: Time of administration of Corifollitropin Alfa
Registration Number
NCT03939403
Lead Sponsor
Instituto Bernabeu
Brief Summary

This study aims to study the efficiency of using a single injection of Corifollitropin alfa for ovarian stimulation by initiating administration late and without further administration of follicle-stimulating hormone after the 7th day of stimulation compared to conventional ovarian stimulation using Corifollitropin alfa (drug administration 5 days after cessation of hormonal contraceptive and supplementation with follicle-stimulating hormone daily administration from the 8th day of stimulation).

This a controlled randomized clinical study and 180 patients will be recruited (90 per arm) and the primary study outcome is the number of obtained oocytes.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
180
Inclusion Criteria
  • Eligible for oocyte donation program
  • Age between 18 and 32 years old
  • BMI >18 and <30
  • Antral follicle count >12 (summing both ovaries)
  • Presence of both ovaries
  • Ability to participate in and comply with study protocol
  • Signed informed consent
  • No treatment with ovulation stimulators in the 3 months prior to the start of stimulation.
Exclusion Criteria
  • Diagnosis of endometriosis at any stage
  • AFC >20
  • Polycystic ovary syndrome
  • Concurrent participation in another study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
7-days pill free intervalTime of administration of Corifollitropin Alfa-
Primary Outcome Measures
NameTimeMethod
Number of oocytesAt the end of stimulation

Number of oocytes after stimulation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Instituto Bernabeu

🇪🇸

Alicante, Spain

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