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NCT01268696 Clinical Trial

Genetic Assessment of the Patients With Metabolic Syndrome

Metabolic Syndrome Clinical Trial

— GENMetS  

Official title:
Genetic Assessment of the Patients With Metabolic Syndrome in Polish Population

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT01268696
Other study ID # RNN/202/10/KE
Secondary ID
Status Active, not recruiting
Phase N/A
First received December 28, 2010
Last updated July 20, 2011
Start date December 2010
Est. completion date January 2015

Study information
Verified date December 2010
Source Medical Universtity of Lodz
Contact n/a
Is FDA regulated No
Health authority Poland: Ethics Committee
Study type Observational

Clinical Trial Summary

Metabolic syndrome is a combination of medical disorders that increase the risk of developing cardiovascular disease and diabetes. The exact mechanisms of the complex pathways of metabolic syndrome are not yet completely known. The pathophysiology is extremely complex and has been only partially elucidated. Most patients are older, obese, sedentary, and have a degree of insulin resistance. Stress can also be a contributing factor. The most important factors are:

weight, genetics, aging, sedentary lifestyle,excess caloric intake. In our study we will assess the role of some polymorphisms in the pathology of metabolic syndrome.

Description:

Eligibility criteria to the study:

- patients with metabolic syndrome

- with written consent

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 300
Est. completion date January 2015
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- patients with metabolic syndrome according to IDF,AHA and NHLBI 2009

Exclusion Criteria:

- diabetes type 1

- cancer

- not consent

- steroid therapy

- alcohol or drug abuse

- chronic inflammatory disease

- pregnancy or lactation

- severe hypothyroidism

- immunosuppressive treatment

- operation or severe injury during the last month

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Poland Department of medical biotechnology Medical University of Lodz Lodz

Sponsors (1)
Lead Sponsor Collaborator
Medical Universtity of Lodz

Country where clinical trial is conducted

Poland, 

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