Actively Recruiting
The Buzdar Technique for Pulmonary Parenchymal Chest Tube Removal: Prospective Evaluation of a Novel Minimally Invasive Protocol
Led by University of Health Sciences Lahore · Updated on 2026-01-13
300
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Chest tube thoracostomy is a critical procedure used to treat conditions like pneumothorax, hemothorax, empyema, and pleural effusions, especially in trauma and thoracic surgery. Despite its frequent use worldwide, complications occur in 20% to 40% of cases, with pulmonary parenchymal chest tube (PPcT) insertion being a rare but serious issue. This procedure is particularly important in Pakistan due to high rates of chest trauma and pneumothorax, yet minimally invasive removal methods for PPcT are lacking. The Buzdar Technique was developed as a novel, minimally invasive, three-stage method to safely remove these tubes without surgery. The Buzdar Technique involves three phases: first, leaving the chest tube in place for about two weeks to allow healing and fibrosis of the lung tissue; second, a gradual initial retraction of 2 cm with optional rotation under imaging and clinical observation, followed by 24 hours of monitoring; and third, weekly staged retractions of 2 cm until the tube is fully removed from the pleural cavity. This approach avoids the need for surgical interventions like thoracotomy or video-assisted thoracic surgery (VATS). Patients receive antibiotic coverage and negative pressure drainage during the process to support healing. Participants in this prospective cohort study will be monitored clinically and with imaging throughout the removal process. Data collected will include demographics, procedural details, complications, lung recovery, and overall outcomes. The primary goal is to achieve complete tube removal without causing pneumothorax, air leak, bleeding, or need for surgery. The study will assess safety, effectiveness, and lung function recovery over the treatment period, with patient follow-up lasting up to two weeks or longer depending on individual progress.
CONDITIONS
Brief Title
The Buzdar Technique
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older with confirmed intraparenchymal chest tube placement on chest CT or X-ray
- Hemodynamically stable patients suitable for conservative staged removal
- Patients providing informed consent
You will not qualify if you...
- Patients requiring immediate thoracotomy due to massive bleeding or large bronchopleural fistula
- Patients with uncorrectable coagulopathy or unstable cardiopulmonary status
- Patients refusing participation or lost to follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 2 weeks
Participants have the chest tube left in place for approximately 2 weeks to allow localized fibrosis and sealing of the injured lung tissue, with clinical observation and radiologic monitoring.
Clinical observation and radiologic monitoring during hospitalization or short-stay observation
Duration - 1 day
After the initial 2-week period, the chest tube is retracted about 2 cm under sterile conditions, with optional rotation to free adhesions. Participants are monitored for 24 hours with vital signs and chest X-ray evaluation.
1 day inpatient observation with post-retraction chest X-ray
Duration - Variable weekly duration until complete removal
Participants undergo weekly 2 cm chest tube retractions under radiologic and clinical supervision with 24-hour monitoring and chest X-rays at each stage until the tube is completely removed.
Weekly visits with 24-hour monitoring and chest radiographs
Trial Site Locations
Total: 1 location
1
Services Hospital Lahore
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
Z
Zeeshan Sarwar, MBBS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here