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Clinical Trial Summary

Study Population: 4000 stable COPD patients, and among them approximately 2000 subjects with hypertension and/or type 2 diabetes complications. Design: Cohort Study Primary Objectives: The primary objective of this study is to access the effectiveness of IDM on changes in FEV1 from baseline to the 24th week visit in patients with COPD. Statistical Analysis: We plan to compare demographic differences between groups based on whether the data conformed to normal distribution and satisfied variance chi-square, and proposed to calculate p-values using the t-test or non-parametric test for continuous data and Person's χ² or non-parametric test for categorical data. A two-sided p-value < 0.05 is considered statistically significant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06456749
Study type Observational [Patient Registry]
Source China-Japan Friendship Hospital
Contact Ting Yang, MD
Phone 84206272
Email zryyyangting@163.com
Status Not yet recruiting
Phase
Start date June 17, 2024
Completion date March 15, 2026

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