UnknownNot applicableNCT04913415

A Study to Evaluate Routine Chest Tube Management After Minimally Invasive Lung Surgery

Chest tubes are routinely required after surgical procedures for lung cancer. This device is a flexible plastic tube that is inserted through the chest wall to remove air or fluid from around your lungs after surgery for lung cancer. There are two general strategies associated with the clinical management of chest tubes, active and passive suction. If suction is compared to driving a car, active suction is similar to pressing the gas pedal while passive suction is like letting your car move on its own. The suction approach taken by surgeons largely depends on how they were trained and some personal biases and beliefs. However there is no general consensus about which chest tube management strategy is best. This research aims to compare two settings on a digital drainage system, a low suction (LS) mode - passive suction - and standard suction (ss) mode - active suction. From the data collected, the researchers will analyze whether LS or SS will lead to a better recovery after surgery.

Checked against the public recordLast updated Apr 25, 2024 · Source: ClinicalTrials.gov

StatusUnknown
PhaseNot applicable
U.S. locations1
SponsorAllegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Not applicable
Sponsor
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
Interventions being studied
Other: Low Suction Strategy of Chest Tube Management; Other: Standard Suction Strategy of Chest Tube Management
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
03
Public criteria

Who may be able to participate

Inclusion Criteria: 1. Patients who are undergoing lobectomy or segmentectomy 2. Patients undergoing wedge resection to diagnose, or as definitive therapy for a lung nodule/cancer. 3. Able to understand and sign consent Exclusion Criteria: 1. Patients undergoing pneumonectomy or bilobectomy 2. Patients undergoing resection for inflammatory conditions such as aspergillosis 3. Patients undergoing diagnostic wedge resection for interstitial lung disease 4. Patients undergoing redo-VATS or thoracotomy on the same side as current planned resection 5. Patients found to have a "frozen chest" at the time of surgery, requiring extensive adhesiolysis, 6. Patients who are discovered to have metastatic disease during the operation, so that resection is no longer indicated. 7. Patients where a clinical decision to place more than one chest-tube is made

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Allegheny General HospitalPittsburgh, Pennsylvania

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Apr 25, 2024. Always confirm current availability with the study team.

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