- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02087410
Serum Ghrelin in Polycystic Ovary Syndrome
March 13, 2014 updated by: amr hesham el etreby
Ghrelin in Polycystic Ovary Syndrome
measuring serum gherlin in polycystic ovary syndrome patients and compare it to healthy levels
Study Overview
Status
Unknown
Conditions
Detailed Description
two groups one healthy and other with pco measure ghrelin level in both of them to find relation between pco and ghrelin
Study Type
Observational
Enrollment (Anticipated)
84
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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-
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Cairo, Egypt
- Maternity Hospital
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Contact:
- amr h eletreby, resident
- Phone Number: 0096659000850
- Email: mhmdzdn@Gmail.com
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Contact:
- amr h eletreby, resident
- Phone Number: 00966566255584
- Email: eletreby.amr@Gmail.com
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Principal Investigator:
- amr h eletreby, mbbch
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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
20 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Forty two patients with polycystic ovarian syndrome and forty two healthy subjects will be recruited from the outpatient clinic Ain Shams University Maternity Hospital.
Description
Inclusion Criteria:pco women
- At least 12 months of infertility.
- Patients with polycystic ovarian syndrome according to Rotterdam criteria:
Exclusion Criteria:
- Patients with hyperprolactinemia
- Patients with Cushing's syndrome
- Patients with Congenital or non-classical adrenal hyperplasia
- Patients with hormone secreting tumors.
- Patients with hormonal treatment in the last 3 months.
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
Cohorts and Interventions
Group / Cohort |
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study
patients with polycystic ovary syndrome
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control
healthy patients serves as control group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
relationships between circulating ghrelin and the clinical and biochemical manifestations of PCOS
Time Frame: after 6 monthes
|
Analysis of levels of ghrelin in study group
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after 6 monthes
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: amr eletrby, MBBCH, ain shams universty maternity hospital
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
April 1, 2014
Primary Completion (Anticipated)
October 1, 2014
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
March 12, 2014
First Submitted That Met QC Criteria
March 13, 2014
First Posted (Estimate)
March 14, 2014
Study Record Updates
Last Update Posted (Estimate)
March 14, 2014
Last Update Submitted That Met QC Criteria
March 13, 2014
Last Verified
March 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ghrelin
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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-
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