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Caduet and TLC Intervention in Metabolic Syndrome

Metabolic Syndrome Clinical Trial

Official title:
Effect of Caduet and TLC Intervention on Metabolic Parameters

Clinical Trial Summary

To evaluate the effectiveness of Caduet in addition to therapeutic life-style change (TLC) intervention in resolving metabolic syndrome fifty three individuals were randomized to TLC intervention study with or without Caduet therapy for 12 months. The participants underwent monthly visits with investigators to obtain vital signs, and to undergo TLC counseling. Metabolic parameters were measured before and after intervention.

Clinical Trial Description

Single center, investigator driven, double blinded, randomized with Caduet 5/10mg vs placebo. The participants visited with investigators on a monthly bases to evaluate the BP, weight, and obtain the waist measurements, and counseling. OGTT was performed at the beginning and the end of the study. Lipid and glucose parameters were measured 5 times in duration of the study period.

Exercise physiologists and dietitians completed the baseline evaluations and provided recommendations throughout the study period in person, via phone or e-mail: per subject preference. VO2 max was measured at the beginning and end of the study. Pedometers dispensed to encourage physical activity. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03504735
Study type Interventional
Source The University of Texas Medical Branch, Galveston
Contact
Status Completed
Phase Phase 4
Start date May 1, 2005
Completion date February 28, 2016
View Details
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