drugset / Trial / NCT07409129

Tubeless Strategy for Enhanced Recovery After Sublobar Resection

NCT07409129 ↗

RandomizedParallel-groupSingle-blindTreatment

Summary

This is a prospective, randomized controlled clinical trial conducted at a single center. The study aims to evaluate whether a "tubeless" strategy can enhance recovery for patients undergoing minimally invasive thoracoscopic sublobar resection (wedge or segment resection) for small lung nodules. Participants will be randomly assigned to one of two groups: * The experimental group will receive the "tubeless" strategy, which includes non-endotracheal intubation anesthesia (using a laryngeal mask) and no routine chest tube drainage after surgery. * The control group will receive the traditional strategy, which includes double-lumen endotracheal intubation anesthesia and routine chest tube drainage. The main goal is to compare the rate of achieving high-quality fast-track recovery at 24 hours after surgery between the two groups. This study will provide evidence on whether the tubeless approach can help patients recover faster and more comfortably without compromising safety.

Timeline

Start
2026-02-01
Primary completion
2026-06-01
Completion
2026-09-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Background Ropivacaine Other / unclassified — —

Indications