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Premature Luteinization Prevention by GnRH Antagonist in Patients Undergoing IUI (LP)

I

IVI Madrid

Status

Completed

Conditions

Infertility

Treatments

Drug: Ganirelix

Study type

Observational

Funder types

Other

Identifiers

NCT00780858
IVIMAD-JMS-09-2008-02

Details and patient eligibility

About

Premature luteinization in patients undergoing IUI can occur in up to 24% of cycles. These patients, according to recent data, have a lower pregnancy rate than controls. The possibility to avoid premature luteinization with GnRH antagonist may restore the chances of achieving a pregnancy in these women.

Full description

The purpose of this study was to investigate whether a subset of patients benefits from GnRHa administration during IUI. PL was tested for in patients who were undergoing artificial insemination procedures, and the effect of GnRHa on PR in patients who

Enrollment

662 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • previous failed IUI cycle with premature luteinization

Exclusion criteria

  • 39 years or older
  • not eligible for IUI (patent tubes, > 3 million capacitated spermatozoa)
  • 4 previous IUI cycles

Trial design

662 participants in 2 patient groups

Ganirelix
Description:
Patients with premature lutenization (progesterone \>1,2 ng/ml) who did not get pregnant during the first IUI underwent a second IUI.
Treatment:
Drug: Ganirelix
Control
Description:
Patients without premature lutenization (progesterone \>1,2 ng/ml) underwent a only one IUI.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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