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A comparison of different dose intravenous lidocaine for prevent cough and sore throat after awakening from general anesthesia, a double blind randomized control trial

A comparison of different dose intravenous lidocaine for prevent cough and sore throat after awakening from general anesthesia, a double blind randomized control trial

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200325003
Enrollment
184
Registered
2020-03-25
Start date
2020-02-05
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Cough after awakening from general anesthesia&#44

Interventions

A comparison of different dose intravenous lidocaine for prevent cough and sore throat after awakening from general anesthesia&#44
a double blind randomized control trial
Experimental Drug
A comparison of different dose intravenous lidocaine for prevent cough and sore throat after awakeni

Sponsors

Phramongkutklao Hospital
Lead Sponsor
Phramongkutklao Hospital
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: • agree to receive treatment according to the research plan • undergoing surgery By choosing the method of anesthesia and endotracheal tube • Age 18-65 years • ASA I-II (patients who do not have any underlying disease or have underlying disease that can control the symptoms and do not have severe complications) • able to read, write and understand Thai

Exclusion criteria

Exclusion criteria: • Refusing to participate in research • have a history of hypersensitivity to lidocaine or other local anesthetics • Patients with abnormal liver and kidney function • Patients with congestive heart failure, recent myocardial infarction and cardiac arrhythmia such as AV block, atria fibrillation, Ventricular tachycardia • Problems with communication using language (language barrier) • Patients with a history of asthma or emphysema • Patients with a history of upper respiratory infections within 2 weeks. • Patients with high blood pressure and receiving ACEI • Patients who are pregnant Or is breast-feeding • The patient undergoes emergency surgery. • • Patients with adverse effects from coughing, such as patients with increased intracranial pressure and rupture globe • ASA classification 3 and above

Design outcomes

Primary

MeasureTime frame
The effect of intravenous different lidocaine dose that use before extubation about the cough 05/12/2020 four-point scale postoperative room, grade 0 = no coughing, grade 1 = moderate coughing, grade 2 = m

Secondary

MeasureTime frame
The effect of intravenous different lidocaine dose that use before extubation about sore throat 05/12/2020 Four-point scale at 1 hr. postoperative, grade 0 no sore throat, grade1 mild, grade2 moderate, grade

Countries

Thailand

Contacts

Public ContactChanathip Ajavananda

Phramongkutklao Hospital

bonuschanathip@gmail.com0935565424

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026