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A randomized controlled study of the application of single chamber, three chamber and digital chest drainage device for air leakage after lung surgery

A randomized controlled study of the application of single chamber, three chamber and digital chest drainage device for air leakage after lung surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109981
Enrollment
Unknown
Registered
2025-09-28
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

air leak patients after pulmonary resection

Interventions

Three-lumen chest drainage group:Three-lumen chest drainage
Digital chest drainage group:Digital chest drainage
Single-lumen chest drainage group:Single-lumen chest drainage

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years old; 2. According to the surgical criteria of the 8th edition of People's Health Publishing House, the main criteria for patients with preoperative blood pressure controlled below 160/100mmHg, blood glucose controlled between 5.6-11.2 mmol/L, and normal functions of major organs such as heart, lung, liver, and kidney are as follows: i. Goldman index grade 1-2 (see Annex 1 for detailed criteria); ii. Postoperative predicted FEV1>= 40% and DLCO>= 40%; iii. Total bilirubin =60ml/min; 3. Lobectomy or partial lobectomy (including segmentectomy and wedge resection); 4. Only a single thoracic drainage tube was placed at the end of the operation; 5. The evaluation before randomization was performed within 24 hours after surgery, and bubbles were found to overflow in the single-chamber chest drainage tube when coughing, but no bubbles were found when breathing hard. 6. All relevant examinations were completed within 28 days before surgery. 7. Patients who can understand the study and have signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Tension pneumothorax occurred within 24 hours after operation; 2. Transfer to the intensive care unit before randomization; 3. Unplanned reoperation for various reasons within 24 hours after operation; 4. Pneumonectomy; 5. Previous history of lung surgery; 6. Pregnant or lactating women; 7. Active bacterial or fungal infections that are difficult to control; 8. Severe interstitial pneumonia, pulmonary fibrosis, or emphysema; 9. History of severe heart disease, heart failure, myocardial infarction, or angina within the past 6 months. 10. Severe mental illness; 11. Other circumstances considered by the investigator to be inappropriate for this study.

Design outcomes

Primary

MeasureTime frame
Duration of chest tube drainage;

Secondary

MeasureTime frame
Economic indicators;degree of satisfaction;patien report outcome;Re-catheterization rate;

Countries

China

Contacts

Public ContactBin Hu

Sichuan Cancer Hospital

hubin@scszlyy.org.cn+86 180 8100 6537

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026