Luteal Phase Commencing of Growth Hormone

This study has been completed.
Sponsor:
Collaborator:
Ren-Tıp ART Center, Bursa, Turkey
Information provided by:
Gulhane School of Medicine
ClinicalTrials.gov Identifier:
NCT00561769
First received: November 19, 2007
Last updated: November 20, 2007
Last verified: November 2007
  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

Ages Eligible for Study:   20 Years to 40 Years
Genders 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

ClinicalTrials.gov Identifier: NCT00561769     History of Changes
Other Study ID Numbers: GATA 2005-21
Study First Received: November 19, 2007
Last Updated: November 20, 2007
Health Authority: Turkey: Ministry of Health

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
Pharmacologic Actions

ClinicalTrials.gov processed this record on July 29, 2014