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NCT Number: NCT04670523

Early Postoperative Day 0 Chest Tube Removal After Thoracoscopic Minor Surgeries

The safe conditions for early chest tube removal have been progressively questioned and redefined around reliable digital air flow criteria and extension of liquid threshold accepted. Nevertheless, in current practice, the chest tube remains in restricting early mobilization and optimal compliance with ERAS programme, during the first crucial 24 h after surgery. Thus, to go further, the investigators decide to assess in this study the safety of POD 0 chest tube removal after minor thoracic operations in patients in health condition tolerating operation and anesthesia.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital of Bern, Inselspital

Bern, 3013, Switzerland

Location status: Recruiting

Location contact

Patrick Dorn, PD

CONTACT

[email protected]

0041 31 632 37 45 ext. 0797696216

About this study

Chest tube management is a key element of postoperative care after thoracic surgeries for different indications. During the last decade, minimally invasive surgery and enhanced recovery after surgery (ERAS) programmes have radically changed the equation of recovery, contributing to reduce postoperative morbidity and enhance quality of life, but the chest tube remains its Achilles heel, still providing postoperative pain and impairing pulmonary function. In this view, early chest tube removal has been widely promoted not only for its economic benefits on length of stay but also for improving quality of life and potentially reducing postoperative complications. In parallel, the change from traditional chest drainage devices to electronic devices has also enabled a more accurate air leak measurement with reduction of interobserver variability, decreased chest drainage duration and shortened LOS. The safe conditions for early chest tube removal have been progressively questioned and redefined around reliable digital air flow criteria and extension of liquid threshold accepted. Nevertheless, in current practice, the chest tube remains in restricting early mobilization and optimal compliance with ERAS programme, during the first crucial 24 h after surgery. Thus, to go further, the investigators decide to assess in this study the safety of POD 0 chest tube removal after minor thoracic operations in patients in health condition tolerating operation and anesthesia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Thoracoscopic extra-anatomical lung resection (surgical lung biopsy)
  • Thoracoscopic pleural biopsy
  • Signed consent
  • Age of majority

Exclusion criteria

  • Anatomical resection
  • Empyema
  • Pleural effusion
  • Pleurodesis
  • Vulnerable persons (Pregnant women, Children and adolescents)

Treatment and study plan

Early postoperative day 0 (POD 0) chest tube removal.

Procedure

Chest tube removal is a standard bedside intervention after lung resections. Its time point is normally defined according a traditional standard airleak threshold. Traditionally, in our department this threshold will be respected not earlier than 1 day after the operation. The patients of the study group are getting their chest tube removed according to our current airleak protocol (Flow <20 mL/ min on digital suction device) but already in the operating room after wound closure (POD 0). If airleak is persisting than chest tube removal will be performed according to the traditional protocol not earlier than on postoperative day 1 (POD 1).

Chest tube removal according to traditional standard protocol not earlier than on postoperative day 1 (POD 1).

Procedure

Chest tube removal according to traditional standard protocol not earlier than on postoperative day 1 (POD 1).

Primary outcomes

  1. 1. Pneumothorax requiring chest tube reinsertion

    Time frame: Pneumothorax 2 hours after chest tube removal between postoperative day 0 and 30 (POD 0 - 30)

    Number of patients with pneumothorax requiring chest tube reinsertion after removal of initial chest tube

  2. 2. Pleural effusion requiring thoracocentesis

    Time frame: Pleural effusion 2 hours after chest tube removal between POD 0 and 30

    Number of patients with pleural effusion requiring thoracocentesis after removal of first chest tube

  3. 3. Prolonged air leak > 5 days

    Time frame: Chest tube removal between POD 6 and 30

    Number of patients with persisting air leak longer than 5 days

  4. 4. Re-admission or reoperation due to pleural complication

    Time frame: Up to 1 month after first operation

    Number of patients re-admitted to a hospital after first hospitalization

Secondary outcomes

  1. 1. Cardiopulmonary complications (Pneumonia, Atrial fibrillation, ARDS)

    Time frame: Up to 1 month after initial operation

    Number of patients with cardiopulmonary complications (Pneumonia, Atrial fibrillation, ARDS) after operation

  2. 2. Re-operation

    Time frame: Up to 1 month after initial operation

    Number of patients requiring a re-operation after initial operation

  3. 3. Length of drainage (days)

    Time frame: Up to 1 month after initial operation

    Average of time with chest tube in site

  4. 4. Length of stay (days)

    Time frame: Up to 1 month after initial operation

    Average of time in hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Patrick Dorn, PD

CONTACT

[email protected]

0041 31 632 37 45 ext. 0797696216

Sponsors and collaborators

Lead sponsor

Insel Gruppe AG, University Hospital Bern

Other

Registry information

Official study title

Early Postoperative Day 0 Chest Tube Removal After Thoracoscopic Minor Surgeries. A Randomized Controlled Clinical Trial.

Acronym: CTremoval

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Dec 17, 2020
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.