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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00561769
Other study ID # GATA 2005-21
Secondary ID
Status Completed
Phase Phase 4
First received November 19, 2007
Last updated November 20, 2007
Start date January 2005
Est. completion date November 2007

Study information

Verified date November 2007
Source Gulhane School of Medicine
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Observational

Clinical Trial Summary

Commencing of growth hormone in luteal phase when follicular cohort for the next cycle is being gathered may increase mature oocytes in poor responder


Recruitment information / eligibility

Status Completed
Enrollment 61
Est. completion date November 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Poor responder

Exclusion Criteria:

- FSH >20 IU

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
Norditropin pen
12 IU per day

Locations

Country Name City State
Turkey Ren Tip ART Center Bursa

Sponsors (2)

Lead Sponsor Collaborator
Gulhane School of Medicine Ren-Tip ART Center, Bursa, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary mature oocyte number 2 years
Secondary pregnancy rate 2 years
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