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GnRH Antagonist to Prepare Recipients for Embryo Transfer

I

Institute for Human Reproduction (IHR)

Status

Completed

Conditions

Infertility

Treatments

Drug: GnRH Antagonist (Cetrotide)

Study type

Interventional

Funder types

Other

Identifiers

NCT00460642
IND 74,817

Details and patient eligibility

About

26% of all ART cycles performed in the USA in 2003 (CDC data) are frozen embryo transfers (FET) and transfer of embryos resulting from egg donation (ED) to recipients. The typical protocol used to prepare a recipient for ET involves GnRH agonist (Lupron, Tap Pharmaceuticals) to down regulate the patient. A GnRH antagonist, such as Cetrotide (EMD Serono), is comparable to GnRH agonist and FDA approved to prevent spontaneous ovulation with ART treatment, and its usage decreases significantly the number of injections that the patient receives with treatment. The working hypothesis for this study is that the GnRH antagonist (Cetrotide) can be used instead of an agonist to achieve effective down regulation in FET and ED cycles. Presumably, patients will prefer Cetrotide over Lupron because of the markedly fewer injections required.

Enrollment

130 estimated patients

Sex

Female

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • History of infertility before cryopreserving the embryos or inability to conceive from her own oocytes (based on age and/or a serum FSH > 15 IU/L).
  • Any patient desiring to become pregnant as a result of transferring frozen-thawed embryos generated using her own or donor oocytes.
  • Subject is in good health as determined by the Investigator on the basis of medical history, physical examination and laboratory screening tests.
  • A negative pregnancy test prior to starting treatment with estrogens.

Exclusion criteria

  • Women with a history of liver and/or kidney disease
  • Hypertension: systolic pressure over 180 mm Hg or diastolic pressure over 105 at any study visit, measured twice 6 hours apart despite active treatment for hypertension.
  • Liver function tests of two times than the upper limit of normal
  • Women with active sever endometriosis.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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