Current partner codePEPTIDESDE
NCT02796105·Phase 4·INTERVENTIONAL

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

Status

Completed

Phase

Phase 4

Enrollment

232

Locations

1

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

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

Interventions

Treatment arms and agents.

DRUG

Progevera

DRUG

Orgalutran

Timeline

From registration to results.

  1. First posted

    Jun 10, 2016

  2. Study start

    Jun 2016

  3. Primary completion

    Jul 2017

  4. Study completion

    Jul 10, 2017

  5. Results posted

    Not reported

  6. Registry updated

    Sep 13, 2017

Outcomes

What the study measures.

Primary outcomes

donor ovarian response

Time frame · 1 month

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
35 Years
Sex
FEMALE
Healthy volunteers
No

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

Study locations

1 registered sites.

Spain. Showing up to 24 locations stored in the fast local snapshot.

Clinica Eugin

Barcelona, Spain

Related trials

More studies on Ganirelix.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.