Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07338019

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Healing and Fibrosis Phase

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

Initial Retraction and Assessment

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

Sequential Retractions and Final Removal

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

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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

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