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Randomized controlled trial for the management of air leakage after pulmonary resection

Randomized controlled trial for the management of air leakage after pulmonary resection - Randomized controlled trial for the management of air leakage after pulmonary resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051770
Enrollment
40
Registered
2023-09-01
Start date
2023-09-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Air leakage after pulmonary resection

Interventions

GroupD: Digital drainage system. Thopaz is used for chest drainage in physiological pressure mode(=-8cmH2O) GroupA: Analog chest drainage system. Analog chest drainage system is used in water seal.

Sponsors

Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Yamadaoka, Suita, Osaka, Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) The patients who underwent anatomical pulmonary resection (segmentectomy,lobectomy,and bilobectomy) (2) The patients who have postoperative air leakage more than 30ml/min detected by thopaz on the third day after surgery (3) The patients who consent to the includion of this study in writing

Exclusion criteria

Exclusion criteria: (1) The patients who underwent pneumonectomy (2) The patients who underwent lung resection with bronchus or vessel plasty (3) The patients who underwent combined resection of adjacent organs in treatment (4) The use of positive pressure ventilation after surgery (5) The patients who already have therapeutic interventions for postoperative air leakage before including this study (6) The patients who are privided more than two chest drainage tubes in operation room (7) Chylothorax or empyema is detected before including this study (8) The volume of chest drainage is more than 300ml/day (9) The reserch responsible doctor or investigator judges the inadequateness of including

Design outcomes

Primary

MeasureTime frame
The duration of postoperative drainage

Secondary

MeasureTime frame
The duration of postoperative air leakage

Countries

Japan

Contacts

Public ContactTakashi Hiroshima

Osaka University Graduate School of Medicine, Yamadaoka, Suita, Osaka, Japan Department of General Thoracic Surgery

t-hiroshima@thoracic.med.osaka-u.ac.jp0668793152

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026