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Clinical Trial Summary

Through this randomized controlled clinical trial, we aim to identify whether there is a difference in the incidence of 24 hour pneumothorax after chest tube removal, in two blindly randomized groups of patients: The first group with chest tube clamping 6 hours prior to removal, and the second group there will be no chest tube clamping. The data will be prospectively collected from patient records from the National Institute of Respiratory Diseases Ismael Cosío Villegas.


Clinical Trial Description

Patients with an indication of chest tube removal will be randomized to two possible arms: clamping (for 6 hours before removal) or not clamping (immediate removal). Incidence of 24hour pneumothorax after chest tube removal will be recorded. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05243316
Study type Interventional
Source National Institute of Respiratory Diseases, Mexico
Contact
Status Completed
Phase N/A
Start date December 22, 2021
Completion date April 15, 2023

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