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Clinical Trial to Assess the Preventive Effects of Cetylpyridinium Chloride on Sarcopenia — CPC2  

Sarcopenia Clinical Trial

Official title:
Randomized, Double Blinded, Placebo-controlled Trial to Assess the Preventive Effects of Cetylpyridinium Chloride on Sarcopenia

Clinical Trial Summary

This study is to assess the impact on the prevention of sarcopenia after taking cetylpyridinium chloride targeting the patients of pre-sarcopenia or sarcopenia over the age of 60

Clinical Trial Description

75 people that meet the inclusion criteria on screening test are assigned to one of three groups by randomization. They take the medication for four weeks under doubleblind. Two study groups take cetylpyridinium chloride of 1.5mg, 4.5mg daily for four weeks. Control group takes the placebo for the same period. The main outcome variables are measured and compared respectively in baseline, immediately after dosing end and two weeks, four weeks after the end of administration. Finally cetylpyridinium chloride is verified whether it has a preventive effect on sarcopenia and set an appropriate dose. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02575235
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase Early Phase 1
Start date October 1, 2015
Completion date July 1, 2016
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