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A comparative study between the effects of lidocaine 2% around the outer surface of endotracheal tube cuff and TCI remifentanil on coughing , agitation and hemodynamics during extubation after thyriod surgery: a Randomized Controlled Trial

A comparative study between the effects of lidocaine 2% around the outer surface of endotracheal tube cuff and TCI remifentanil on coughing , agitation and hemodynamics during extubation after thyriod surgery: a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038653
Enrollment
Unknown
Registered
2020-09-27
Start date
2020-10-12
Completion date
Unknown
Last updated
2020-12-14

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

Conditions

thyriod goiter

Interventions

Remifentanil group (R group):TCI 2.0ng/ml remifentanil during extubation
Lidocaine group (L group):Lidocaine 2% around the outer surface of endotracheal tube cuff during extubation

Sponsors

Guangdong Provincial Hospital of Tradition Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) 18-65 years old female; 2) ASA grade I-II; 3) Patients with thyriod surgery who are to be operated on under general anesthesia by endotracheal intubation; 4) Obtain the informed consent of the patient and/or the legal guardian and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) Use the NIM standard reinforced EMG endotracheal tube & NIM contact reinforced EMG endotracheal tube for nerve monitoring; 2) Mental disorders, inability to communicate, difficult airways, high perioperative risk of reflux aspiration; 3) A history of chronic respiratory disease (such as chronic obstructive pulmonary disease or asthma), recent respiratory infection, chronic cough, smoking; 4) Serious cardiovascular, liver, or kidney disease; 5) Prior laryngeal or tracheal surgery, local anesthetic allergy, and treatment with beta blockers.

Design outcomes

Primary

MeasureTime frame
Cough grading system;

Secondary

MeasureTime frame
Mean arterial pressure and heart rate;the Richmond Agitation-Sedation Scale (RASS);Critical-Care Pain Observation Tool;Sedation Grading System;Visual Analogue Scale;

Countries

China

Contacts

Public ContactPing Li

Department of Anesthesiology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, P. R. China

346036322@qq.com+86 15622149528

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026