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GnRH Agonist and Intrauterine Insemination

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00503217
First Posted: July 18, 2007
Last Update Posted: September 7, 2016
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 (Responsible Party):
Jose Bellver, Instituto Valenciano de Infertilidad, IVI VALENCIA
  Purpose
The aim of this study is to assess whether GnRH agonist administration in the luteal phase improves pregnancy outcome in intrauterine insemination (IUI) cycles.

Condition Intervention Phase
Intrauterine Insemination Drug: Tryptorelin Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Official Title: Effect of GnRH Agonist Administration at the Time of Implantation in Intrauterine Insemination Cycles: A Randomized Controlled Trial

Resource links provided by NLM:


Further study details as provided by Jose Bellver, Instituto Valenciano de Infertilidad, IVI VALENCIA:

Study Start Date: February 2005
Study Completion Date: December 2007
Primary Completion Date: December 2007 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 38 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Women < 38 years old
  • Bilateral tubal patency confirmed by hysterosonography
  • Normal ultrasound scan of uterus and ovaries
  • Normal day 3 basal hormones
  • Motile sperm count after capacitation ≥ 3 mill/ml

Exclusion Criteria:

  • Endometriosis
  • Polycystic ovary syndrome
  • Uterine disease (polyps, myomas and müllerian diseases)
  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): NCT00503217


Locations
Spain
Instituto Valenciano de Infertilidad Spain
Valencia, Spain, 46015
Sponsors and Collaborators
Instituto Valenciano de Infertilidad, IVI VALENCIA
Investigators
Principal Investigator: Jose Bellver, MD Instituto Valenciano de la Infertilidad
Principal Investigator: Elena Labarta, MD Instituto Valenciano de Infertilidad
  More Information

Responsible Party: Jose Bellver, Gynecologist IVI Valencia, Instituto Valenciano de Infertilidad, IVI VALENCIA
ClinicalTrials.gov Identifier: NCT00503217     History of Changes
Other Study ID Numbers: VLC-JB-0205-307-9
First Submitted: July 17, 2007
First Posted: July 18, 2007
Last Update Posted: September 7, 2016
Last Verified: September 2016

Keywords provided by Jose Bellver, Instituto Valenciano de Infertilidad, IVI VALENCIA:
intrauterine insemination
GnRH agonist
implantation

Additional relevant MeSH terms:
Deslorelin
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action