A Prospective, Randomized, Double-blind Study on the Effects of Different Anesthesia Strategies on Postoperative Cough in Patients Undergoing Video-assisted Thoracoscopic Surgery.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFujian Medical University Union Hospital

About this trial

This study aims to systematically evaluate the effects of different anesthesia methods on postoperative chronic cough in lung cancer patients undergoing video-assisted thoracoscopic lung resection (VATS), and to clarify the effectiveness and safety of each anesthesia airway management strategy in reducing the incidence of postoperative chronic cough, shortening the duration of cough, alleviating the severity of symptoms, and improving the postoperative quality of life of patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

planned wedge resection, segmentectomy or lobectomy;

more than 18 years old;

American Society of Anesthesiologists (ASA) grade ≤Ⅲ;

body mass index (BMI) ≤24 kg/m2;

Disqualifiers

(1) patients who refuse surgery and/or anesthesia; (2) preoperative pulmonary infection; (3) previous history of ipsilateral surgery or other medical history that may cause extensive pleural adhesions; (4) phrenic nerve palsy on the non-operative side; (5) patients with high risk of preoperative reflux (fasting <6 hours) or gastroesophageal reflux disease; (6) patients with heart, kidney, liver and other organ dysfunction and surgical contraindications; (7) with severe cognitive, psychological and communication disorders.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Patients were randomly grouped

    Other intervention

    All patients included in the study, were randomized

Treatment groups

228 Participants
are divided into 3 treatment groups
Group A: Single-lumen endotracheal intubation groupActive comparator 1 intervention
Group B: Double-lumen endotracheal tube groupActive comparator 1 intervention
Group C: Laryngeal mask groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The incidence of postoperative chronic cough, cough duration and cough severity score were recorded

The perioperative follow-up time points were 1 day, 2 days, 3 days, 7 days, 14 days and 1 month after operation. The follow-up time points of postoperative chronic phase were set at 3 months, 6 months and 12 months after operation.

Time frame
The perioperative follow-up time points were 1 day, 2 days, 3 days, 7 days, 14 days and 1 month after operation. The follow-up time points of postoperative chronic phase were set at 3 months, 6 months and 12 months after operation.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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