Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01125501

Protandim and the Metabolic Syndrome

Protandim and the Metabolic Syndrome: A Preliminary Study to Define Protein Signatures That Change Along With Lowered Oxidative Stress Measured as F2 Isoprostanes or TBARS and Inflammation Measured as hsCRP

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
SomaLogic, Inc. · Industry
Sex
All
Age
40 Years – 60 Years
Healthy volunteers
Accepted

Summary

Protandim will decrease markers of oxidative stress/inflammation in subjects with metabolic syndrome and proteomics will identify protein profiles that correlate with markers or/changes in oxidative stress.

Detailed description

Evaluate the effects of Protandim on protein profile changes and markers of inflammation and oxidation in subjects (40-60 years of age) with the Metabolic Syndrome.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTProtandimThe product Protandim used in this study have ingredients derived from five botanical sources \[Bacopa monniera, Silybum marianum (milk thistle), Withania somnifera (Ashwagandha), Camellia sinensis (green tea), and Curcuma longa (turmeric)\].

Timeline

Start date
2010-04-01
Primary completion
2010-06-01
Completion
2010-06-01
First posted
2010-05-18
Last updated
2017-10-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01125501. Inclusion in this directory is not an endorsement.