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NCT03484663 Clinical Trial

Small Catheter Drainage With Chest Tube Versus Chest Tube Alone After Uniport Video-assisted Thoracoscopic Procedures

Lung Diseases Clinical Trial

— uniportal VATS  

Official title:
Small Catheter Drainage With Chest Tube After Uniport Video-assisted Thoracoscopic Procedures

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03484663
Other study ID # uniport VATS
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2018
Est. completion date July 1, 2019

Study information
Verified date June 2018
Source Assiut University
Contact ali Abdelraouf, residant
Phone 01004396639
Email alioufa32@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Small catheter drainage with chest tube after uniport Video-assisted Thoracoscopic Procedures

Description:

Traditionally an Intercostal Tube is applied intraoperative following VATS procedures to drain the remaining pneumothorax and residual effusion , some of the residual effusion can't drain by intercostal tube which lead to prolonged hospital stay hypothesis that putting an additional small catheter drainage at the most depended part of hemithoracic early removal of chest tube without add more pain or hospital stay to the patient.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 10
Est. completion date July 1, 2019
Est. primary completion date May 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients undergoing uniport video-assisted thoracoscopic surgery at Assiut University Hospital who need intercostal drainage postoperative

Exclusion Criteria:

- Patients who do not need intercostal tube post operative

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• central venous catheter (small catheter drainage)
Insertion central venous catheter ( small catheter drainage ) after uniport vats to decrease hospital stay and to easy drainage after procedure

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants with failure of initial intervention Number of participants with failure of initial intervention , Requiring a second intervention i.e.insert second tube one year
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