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Feasibility and safety of laryngeal mask airway assisted nerve block non-tracheal intubation anesthesia in video-assisted thoracoscopic surgery: a randomized, controlled study

Clinical application of non-tracheal intubation anesthesia in thoracoscopic surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050645
Enrollment
Unknown
Registered
2021-09-01
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Patients scheduled for thoracoscopic surgery

Interventions

Experimental group:Laryngeal mask assisted nerve block
Control group:Dual-chamber bronchial assisted nerve block

Sponsors

The First Affiliated Hospital of USTC Anhui Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Agree to undergo thoracoscopic surgery with simple surgical steps and short time (pneumothorax, bullae, lung wedge resection, thymoma surgery, thoracic sympathetic chain resection)(expected < 5 hours);; 2. Voluntarily participated in this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pulmonary infectious lesions, excessive airway secretions, or hemoptysis; 2. The tumor diameter is greater than 6 cm, the tracheal anatomy is abnormal, or the lesions involve the bronchus; 3. Insufficient blood volume, blood system disease or coagulation mechanism disorder; 4. Difficult airway; 5. Extensive pleural adhesions or a history of lobectomy or partial lung resection; 6. Severe cardiopulmonary dysfunction; 7. Nervous system diseases; 8. Body mass index > 30 kg/m2; 9. ASA >= III; 10. Abnormal platelet and coagulation function; 11. Short-term or long-term use of opioids; 12. The puncture site is infected.

Design outcomes

Primary

MeasureTime frame
Arterial partial pressure of oxygen;Arterial carbon dioxide partial pressure;Lactic acid;PH;The incidence of throat pain ;Postoperative pain score;

Secondary

MeasureTime frame
Surgeon’s satisfaction;Consumption of propofol;Sufentanil consumption;Remifentanil consumption;Number of white blood cells before and after surgery;

Countries

China

Contacts

Public ContactZhou Ling

Anhui Provincial Hospital Erhics Committee on Medical Research

13866702756@163.com+86 13866702756

Outcome results

None listed

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