Comparison of clinical application of 8.5F chest tube continuous open drainage and 16F chest tube conventional clamping and intermittent open drainage after pneumonectomy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900027935

Enrollment

Unknown

Registered

2019-12-05

Start date

2019-12-15

Completion date

Unknown

Last updated

2019-12-10

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

Conditions

Lung Cancer

Interventions

group 1:8.5F chest tube continuous open drainage

group 2:16F chest tube conventional clamping and intermittent open drainage

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed of primary lung cancer by pathology; patients undergo pneumonectomy; R0 resection; intact clinical data.

Exclusion criteria

Exclusion criteria: patients with thoracic cavity closure; complicated with empyema preoperatively; postoperative hemorrhage or continuous leakage that needs undergoing reoperation; severe post-operative complications that need respiratory support; patients with mental disease combing; patients treated with systemic hormone therapy; patients with poor treatment compliance; deemed unfit to attend the trial by investigator.

Design outcomes

Primary

Measure	Time frame
effect of drainage;drainage time;degree of pain within 72h post-operation ;post-operative complications;	—

Countries

China

Contacts

Public ContactXu Shidong

Affiliated Cancer Hospital of Harbin Medical University

kldaxia@126.com+86 13903611962

Outcome results

None listed

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