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Luteal Phase Commencing of Growth Hormone

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00561769
First Posted: November 21, 2007
Last Update Posted: November 21, 2007
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.
Collaborator:
Ren-Tıp ART Center, Bursa, Turkey
Information provided by:
Gulhane School of Medicine
  Purpose
Commencing of growth hormone in luteal phase when follicular cohort for the next cycle is being gathered may increase mature oocytes in poor responder

Condition Intervention Phase
Infertility Drug: Norditropin pen Phase 4

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Growth Hormone co-Treatment Within a GnRH Agonist Long Protocol in Patients With Poor Ovarian Response

Resource links provided by NLM:


Further study details as provided by Gulhane School of Medicine:

Primary Outcome Measures:
  • mature oocyte number [ Time Frame: 2 years ]

Secondary Outcome Measures:
  • pregnancy rate [ Time Frame: 2 years ]

Enrollment: 61
Study Start Date: January 2005
Study Completion Date: November 2007
Groups/Cohorts Assigned Interventions
A
poor responder
Drug: Norditropin pen
12 IU per day

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
poor response to previous COH in the same center
Criteria

Inclusion Criteria:

  • Poor responder

Exclusion Criteria:

  • FSH >20 IU
  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): NCT00561769


Locations
Turkey
Ren Tıp ART Center
Bursa, Turkey, 16200
Sponsors and Collaborators
Gulhane School of Medicine
Ren-Tıp ART Center, Bursa, Turkey
Investigators
Study Director: Tansu Kucuk, Assoc Prof GATA Ankara
  More Information

ClinicalTrials.gov Identifier: NCT00561769     History of Changes
Other Study ID Numbers: GATA 2005-21
First Submitted: November 19, 2007
First Posted: November 21, 2007
Last Update Posted: November 21, 2007
Last Verified: November 2007

Keywords provided by Gulhane School of Medicine:
poor responder
growth hormone
luteal

Additional relevant MeSH terms:
Infertility
Genital Diseases, Male
Genital Diseases, Female
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs