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NCT05358158Completed

Chest dRain rEmoval intrAoperatively afTer thoracOscopic Wedge Resection

Efficacy of Avoiding Chest Drain After Video-assisted Thoracoscopic Surgery Wedge Resection

Source: ClinicalTrials.gov · Last updated 20 Mar 2024

Brief summary (registry, in English)

Chest drain is used routinely after lung surgery. Despite preliminary studies demonstrate the feasibility and safety of intraoperative chest drain removal, these are either retrospective or mainly concerning benign disease. Hypothesis: Participants treated without post-operative chest tube after thoracoscopic wedge resection have less pain, reduced opioid usage without increasing postoperative complications than participants treated with standard post-operative chest tube, and could possibly be discharged earlier.

Status (registry)
Completed
Study type
Interventional
Enrollment
94 (actual)
First submitted
28 Apr 2022
Start date
4 May 2022
Primary completion date
17 Mar 2024
Lead sponsor
Copenhagen University Hospital, Rigshospitalet
Diseases
Lung cancer
NCT number
NCT05358158

What you commit to

  • Study type: Interventional
  • Participants enrolled: 94
  • From 4 May 2022 to the primary completion date, 17 Mar 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Increased risk of post-operative air leak assessed perioperatively by the surgeon (e.g. severe adhesions, bullous/emphysematous lung tissue, defects of the visceral pleura due to iatrogenic or other reasons, suturing in the lung tissue, deep lung resection).

Other illness

  • Increased risk of post-operative bleeding assessed perioperatively by the surgeon (e.g. intraoperative bleeding or oozing).

Other

  • Air leak during intraoperative air leak test.

Who the study is looking for

  • Age ≥18 years.
  • Patients referred for elective three port video-assisted thoracoscopic surgery wedge resection of the lung for suspected or confirmed malignant nodules.
  • first second forced expiratory volume ≥60% of expected.
  • No increased bleeding risk (e.g. preoperative international normalized ratio \>2, overdue discontinuation of anticoagulants according to guidelines by the Danish Society for Thrombosis and Haemostasis, known coagulopathy).
  • Not scheduled for frozen section pathology of wedge resection and subsequent lobectomy.
  • Able and willing to give informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Thomas Decker Christensen
Coordinator of this site? Confirm its status
AarhusDenmarkUnknown status
Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.