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Pilot Study of Safety and Tolerability of Nutrifriend Cachexia in COPD Cachexia

COPD Clinical Trial

Official title:
A 12-Week, Randomised, Placebo Controlled, Multi-Centre, Parallel Group Study Assessing the Safety and Tolerability of Nutrifriend Cachexia (Non-Complete Dietary Formula) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Clinical Trial Summary

SF-K002 is a pilot study in patients with moderate to severe COPD suffering from involuntary weight loss. The study is 12 weeks, double-blinded, placebo controlled and the main objective is to study the safety and tolerability of Nutrifriend Cachexia.

Clinical Trial Description

This study is a 12-week, randomised, parallel group, placebo controlled, multi-centre study. The primary objective is to evaluate the safety and tolerability of Nutrifriend Cachexia in patients with COPD. The secondary objectives of the study are to evaluate effects on body composition, muscle function, daily activity, inflammation, lung function, compliance, appetite and Quality of Life. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02442908
Study type Interventional
Source Smartfish AS
Contact
Status Completed
Phase N/A
Start date May 2015
Completion date June 2016
View Details
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