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NCT05230420 Clinical Trial

Urine Bag Usage Versus Chest Drain Clamping After Lung Resection Surgeries

Pleural Effusion Clinical Trial

Official title:
Urine Bag Usage Versus Chest Drain Clamping After Lung Resection Surgeries

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05230420
Other study ID # 02/REC-CT/2021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date December 25, 2022

Study information
Verified date December 2021
Source Al-Quds University
Contact Firas Abuakar, MD
Phone 052220068
Email firasabuakar@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigators will compare two different approaches of postoperative drainage after the standard water-seal drain has been used efficiently; one is by using urine bag and check it get blown by the leaked air, two is by using clamping of the water seal drain. Investigators will compare them depending on several factors such as; cost effectiveness, hospital stay, duration of putting the drain and more, reinsertion of the chest tube and others.

Recruitment information / eligibility
Status Recruiting
Enrollment 160
Est. completion date December 25, 2022
Est. primary completion date November 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - post lung resection patients (via Uniportal VATS only) - Over the age of 18 - indicated chest tube Exclusion Criteria: - Under the age of 18

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Clamping
Clamping of chest tube
• Urine bag
Attachment of a urine bag to chest tube

Locations
Country Name City State
Egypt Assiut University Assiut
Egypt Tanta University Tanta
Italy European Institute of Oncology Milan
Palestinian Territory, occupied Makassed Hospital Jérusalem-Est

Sponsors (4)
Lead Sponsor Collaborator
Al-Quds University Assiut University, European Institute of Oncology, Tanta University

Countries where clinical trial is conducted

Egypt,  Italy,  Palestinian Territory, occupied, 

Outcome
Type Measure Description Time frame Safety issue
Primary Overall cost The overall cost of the patient's hospital stay 5 to 6 days
Secondary Number of participants with re-accumulation of air after chest tube clamping or attachment to the urine bag An important side effect to be studied up to 5 days
Secondary total number of days with chest drain inserted Number of days chest drain remained inserted up to 5 days
Secondary Number of chest x-rays Total number of chest x-rays up to 5 days
Secondary Number of participants that faced other intervention associated side effects Subcutaneous emphysema, tension pneumothorax and others up to 5 days
Secondary Number of participants with chest tube re-insertion An important side effect up to 5 days
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