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Progevera 10 mg® Versus Orgalutran® in Ovarian Stimulation Cycles of Oocyte Donors

F

Fundació Privada Eugin

Status and phase

Completed
Phase 4

Conditions

Infertility

Treatments

Drug: Progevera
Drug: Orgalutran

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Evaluation of efficacy and safety of medroxiprogesterone acetate (Progevera 10 mg®) versus GnRh antagonist (Orgalutran®) in ovarian stimulation cycles of oocyte donors

Enrollment

232 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Oocyte donors included in the oocyte donation program of Clinica EUGIN.
  • 1st oocyte donation cycle at Clínica EUGIN.

Exclusion criteria

  • Polycistic Ovarian syndrome (PCOs).
  • Estradiol levels on day 2 of menstrual cycle >70 pg/ml.
  • Hormone treatments up to 3 months before the oocyte donation cycle.
  • Medical contraindication to the treatments used in the study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

232 participants in 2 patient groups

Progevera
Experimental group
Description:
Progevera 10 mg
Treatment:
Drug: Progevera
Orgalutran
Active Comparator group
Description:
Orgalutran 0.25 mg
Treatment:
Drug: Orgalutran

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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