- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03587415
Serum Preptin and Amylin Levels in Polycystic Ovary Syndrome Patients
Serum Preptin and Amylin Levels With Respect to Body Mass Index in Polycystic Ovary
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Rize, Turkey, 53000
- Recep Tayyip Erdoğan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
the patients with PCOS
Exclusion Criteria:
Cushing's syndrome 21-hydroxylase deficiency Congenital adrenal hyperplasia Thyroid dysfunction Hyperprolactinemia Diabetes Chronic cardiovascular Hepatic, renal, and hematologic diseases Malignancies Using oral contraceptives, anti-androgens, glucocorticoids, anti-hypertensives, anti-diabetics, calcium supplements and anti-obesity drugs and those who smoke or consume alcohol
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Polycyctic ovary sendrome (PCOS)
these women who have PCOS, we will use their blood samples
|
we will take both of group blood samples to compare them serum preptin and amylin
|
|
Healty groups
These women who have reguler menstrual cycle, no akne or hirsutism, we will use their boold samples
|
we will take both of group blood samples to compare them serum preptin and amylin
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum Preptin and Amylin Levels with Respect to Body Mass Index in Polycystic Ovary Syndrome Patients
Time Frame: six months
|
Serum Preptin and Amylin Levels will compare between groups
|
six months
|
Collaborators and Investigators
Investigators
- Study Director: Senol sentürk, PhD, Recep Tayyip Erdoğan University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 107
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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