- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02036411
Does Clomiphene Citrate Used for Induction of Ovulation Effect Levels of AMH and Inhibin B
January 13, 2014 updated by: Taner A Usta, MD, Bagcilar Training and Research Hospital
100mg clomiphene citrate used for ovulation induction.
The investigators take blood sample at 3 and 10 days of menstruation and count AMH and inhibin B.
Study Overview
Status
Unknown
Conditions
Detailed Description
100mg clomiphene citrate used for ovulation induction.
The investigators take blood sample at 3 and 10 days of menstruation.
AMH and inhibit B level will be measured in serum.
We want to search relation of AMH, inhibin b and ovulation induction.
Study Type
Observational
Enrollment (Anticipated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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İstanbul, Turkey, 34200
- Bagcilar Training and Research Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
Women receiving infertility treatment
Description
Inclusion Criteria:
- Infertility treatment
Exclusion Criteria:
- Previous ovarian surgery
- Single functioning ovary
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Does Clomiphene Citrate Used for Induction of Ovulation Effect Levels of AMH level
Time Frame: 1 week
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: TANER USTA, M.D, Bagcilar Training and Research Hospital, Istanbul, Turkey.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2013
Primary Completion (Anticipated)
January 1, 2014
Study Completion (Anticipated)
January 1, 2014
Study Registration Dates
First Submitted
October 10, 2013
First Submitted That Met QC Criteria
January 13, 2014
First Posted (Estimate)
January 15, 2014
Study Record Updates
Last Update Posted (Estimate)
January 15, 2014
Last Update Submitted That Met QC Criteria
January 13, 2014
Last Verified
January 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BEH GynObs-5
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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