RecruitingNot ApplicableNCT07024433

Tubeless Anesthesia in Preventing Lung Complications in Patients Undergoing Surgery for Early-Stage Lung Cancer

Tubeless Anesthesia in Preventing Contralateral Lung Complications in Patients Undergoing Single-Port Thoracoscopic Surgery for Early-Stage Lung Cancer: A Single-Center, Prospective, Open-Label, Randomized Controlled Trial


Sponsor

Fujian Medical University Union Hospital

Enrollment

224 participants

Start Date

May 25, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The study focuses on evaluating the effectiveness and safety of tubeless anesthesia in single-port thoracoscopic surgery for early-stage lung cancer patients. Traditional anesthesia methods risk postoperative complications like lung injury and respiratory issues. Tubeless anesthesia preserves spontaneous breathing without tracheal intubation, potentially reducing these complications and enhancing recovery. The study aims to compare this technique with traditional methods, assessing its impact on contralateral lung complications, perioperative hemodynamics, complication rates, and recovery speed.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether performing lung cancer surgery using a technique that avoids inserting a breathing tube (called tubeless or non-intubated anesthesia) reduces complications and speeds recovery compared to standard general anesthesia. **You may be eligible if...** - You are between 18 and 70 years old - You are in good health overall (ECOG 0–1) - You have lung nodules being removed through minimally invasive keyhole surgery (single-port thoracoscopy) - Your heart and lung function are adequate **You may NOT be eligible if...** - Your BMI is over 30 (obesity) - You have a difficult or complex airway - You have COPD with a lot of mucus secretion - You are unable to stay calm and awake during the procedure - You have had previous lung surgery with a lot of scar tissue - You have severe low oxygen or high carbon dioxide levels - You received chemotherapy or radiation before surgery Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURETubeless anesthesia

1. Anesthesia Induction: Implement TCI with propofol and remifentanil; insert a laryngeal mask for SIMV ventilation, and monitor vital signs including IBP and end-tidal CO2. 2. Nerve Blocks: Perform ultrasound-guided paravertebral, pleural surface, and vagus nerve blocks using local anesthetics. 3. Anesthesia Maintenance: Adjust remifentanil for spontaneous breathing; maintain propofol and BIS levels; manage heart rate and blood pressure with fluids and medication as needed, without using inhaled anesthetics. 4. Postoperative Analgesia: Provide PCIA with morphine for pain management.

PROCEDURETraditional tracheal intubation

1. Anesthesia induction using propofol, sufentanil, and rocuronium is performed, with DLT or single-lumen tube insertion at BIS≤60 for single-lung ventilation, maintaining appropriate oxygen and ventilation parameters. 2. Anesthesia is maintained with sevoflurane, propofol, and remifentanil, supplementing rocuronium every 30-40 minutes for muscle relaxation, with BIS maintained at 40-60. 3. Post-surgery, ultrasound-guided thoracic paravertebral block and PCIA are used for analgesia, with extubation following standard recovery procedures.


Locations(1)

Fujian Medical University Union Hospital

Fuzhou, Fujian, China

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NCT07024433


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