- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01874912
Human Irisin Concentration in Sarcopenia
June 7, 2013 updated by: K. M. Choi, Korea University
Irisin has been identified as a novel myokine that drives brown-fat-like conversion of white adipose tissue.
In this cross-sectional study, the researches investigated whether serum irisin levels are decreased in patients with sarcopenia compared with control subjects with normal muscle mass, and assessed the association between serum irisin levels and various metabolic parameters.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
406
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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Seoul, Korea, Republic of
- Korea University Guro 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
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients in Korean Sarcopenic Obesity Study (KSOS), an prospective observational cohort study designed to examine the prevalence of sarcopenia and sarcopenic obesity in Korean adults and to evaluate their effects on metabolic disorders and health outcomes.
Description
Inclusion Criteria:
- 20<age<80
- apparently healthy subjects
Exclusion Criteria:
- a history of cardiovascular disease
- diabetes
- stage 2 hypertension
- malignancy
- severe renal or hepatic disease
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 |
|---|---|
|
Serum concentration of irisin in the subjects with sarcopenia
Time Frame: 12 week
|
12 week
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The relationship of serum irisin levels with lipid profiles
Time Frame: 12 week
|
12 week
|
|
The relationship of serum irisin levels with skeletal muscle mass index
Time Frame: 12 wks
|
12 wks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
November 1, 2009
Primary Completion (Actual)
April 1, 2011
Study Completion (Actual)
April 1, 2011
Study Registration Dates
First Submitted
June 3, 2013
First Submitted That Met QC Criteria
June 7, 2013
First Posted (Estimate)
June 11, 2013
Study Record Updates
Last Update Posted (Estimate)
June 11, 2013
Last Update Submitted That Met QC Criteria
June 7, 2013
Last Verified
June 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SO(IRISIN)
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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