- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01884649
Fetuin A in Hashimoto Thyroiditis
Fetuin A as a New Marker of Inflammation in Hashimoto Thyroiditis
Study Overview
Status
Conditions
Detailed Description
Patients ≥ 20 years of age being followed up at the outpatient clinics of the Internal Medicine Department in Medeniyet University Goztepe Training and Research Hospital and fulfilling the eligibility criteria will be included in the study. Approval of the local ethics committee and informed consent of the participants will be received for the study. The study is conducted in accordance with the Declaration of Helsinki. Demographic characteristics, concomitant diseases, smoking and alcohol drinking habits, concomitant medication usage, anthropometric and biochemistry data of the eligible patients will be recorded. Patient group will consist of patients with newly diagnosed Hashimoto thyroiditis and the control group will consist of healthy volunteers.
Groups will be compared according to their demographic, an¬thropometric and biochemistry data and serum fetuin-A levels. In order to detect the relationship between the serum fetuin-A levels and clinical features, correlation analyses will be done.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients newly diagnosed with Hashimoto thyroiditis
Exclusion Criteria:
- Acute infection
- Acute or chronic inflammatory disease
- Anti-inflammatory treatment (non-steroidal anti-inflammatory, corticosteroids etc.)
- Hypoxic situations (chronic obstructive pulmonary disease etc.)
- Severe heart, kidney and liver disease
- Pregnancy
- Endocrine disorders
- Malignancy
- Usage of drug that affects thyroid hormone levels
Study Plan
How is the study designed?
Design Details
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
---|
Group of Hashimoto thyroiditis patients
|
Healty control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Comparison of serum fetuin A levels between patients with Hashimoto thyroiditis and healthy subjects
Time Frame: 1 day (The blood samples were obtained on the same day participants arrived to outpatient clinics.)
|
1 day (The blood samples were obtained on the same day participants arrived to outpatient clinics.)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GEAH-1
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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