Clinical Trials Directory

Trials / Terminated

TerminatedNCT03779516

Effect of Nebulized Lidocaine on Postoperative Sore Throat

Effect of Preoperative Nebulized Lidocaine on Postoperative Sore Throat After Endotracheal Intubation

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Antalya Training and Research Hospital · Other Government
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test the hypothesis that use of preoperative nebulized lidocaine is reduced the incidence of postoperative sore throat after endotracheal intubation.

Detailed description

Adult patients undergoing video-assisted thoracic surgery (VATS) requiring double lumen tube (DLT) endotracheal intubation for one-lung ventilation (OLV) were enrolled in the study. Patients were randomized by means of computer-generated order randomization into two groups: Group C (those who received a saline solution as placebo delivered by nebulization) and Group L (those who received lidocaine delivered by nebulization). At 1, 6 and 24 h after tracheal extubation, an observer blinded to treatments evaluated the patients in terms of sore throat and hoarseness. In addition, Patients' satisfaction, intraoperative and postoperative opioid and analgesics consumption and complaints such as dysphagia, nausea and vomiting were recorded. Hemodynamic variables such as blood pressure and heart rate were also recorded.

Conditions

Interventions

TypeNameDescription
OTHERSalineEffect of saline on postoperative sore throat
OTHERLidocaineEffect of nebulized lidocaine on postoperative sore throat

Timeline

Start date
2018-12-19
Primary completion
2019-04-22
Completion
2019-07-15
First posted
2018-12-19
Last updated
2020-04-30

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT03779516. Inclusion in this directory is not an endorsement.