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Transfer of Fresh Versus Frozen/Thawed Embryos in IVF Cycles Where GnRH Agonist is Utilized for Oocyte Maturation.

This study has been withdrawn prior to enrollment.
(Enrollment difficulties)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00365027
First Posted: August 16, 2006
Last Update Posted: September 4, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
HaEmek Medical Center, Israel
  Purpose
It has been suggested that in IVF cycles where GNRH agonist is utilized for final oocyte maturation in patients at risk of ovarian hyperstimulation, pregnancy rates are reduced. We hypothesize that the use of GNRH antagonist reduces pregnancy rates through an effect on the endometrium and not oocyte quality, therefore better results may be obtained by not returning these embryos in a fresh cycle but rather cryopreserving them and returning them to the uterus and a later stage.

Condition Intervention
Ovarian Hyperstimulation Syndrome Infertility Drugs Female Procedure: Delayed embryo transfer

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by HaEmek Medical Center, Israel:

Primary Outcome Measures:
  • Implantation rate per transfer
  • Pregnancy rate per embryo transfer
  • Implantation rate per IVF cycle
  • Pregnancy rate per IVF cycle

Enrollment: 0
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Woman at risk of ovarian hyperstimulation syndrome in IVF cycles for whom GNRH agonist was utilized for final oocyte maturation

Exclusion Criteria:

  • Patient's refusal to participate
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00365027


Sponsors and Collaborators
HaEmek Medical Center, Israel
Investigators
Study Chair: Eliezer Shalev HaE'mek medical center
  More Information

ClinicalTrials.gov Identifier: NCT00365027     History of Changes
Other Study ID Numbers: 5040706
First Submitted: August 15, 2006
First Posted: August 16, 2006
Last Update Posted: September 4, 2015
Last Verified: September 2015

Keywords provided by HaEmek Medical Center, Israel:
GNRH agonist
ovarian hyperstimulation syndrome
Embryo cryopreservation

Additional relevant MeSH terms:
Infertility
Ovarian Hyperstimulation Syndrome
Genital Diseases, Male
Genital Diseases, Female
Ovarian Diseases
Adnexal Diseases
Gonadal Disorders
Endocrine System Diseases
Deslorelin
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action