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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01082458
Other study ID # 4-2009-0519
Secondary ID
Status Completed
Phase N/A
First received March 4, 2010
Last updated November 18, 2010
Start date February 2010
Est. completion date July 2010

Study information

Verified date November 2010
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Target concentration infusion(TCI) of remifentanil (2.0ng/ml) suppresses the cough induced by endotracheal tube more effectively than intravenous administration of lidocaine (1.5mg/kg).


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date July 2010
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Females older than 20 years old

Exclusion Criteria:

- Patients with acute or chronic respiratory disease, hypertension, gastro-esophageal reflux disease, having preoperative sedatives or mucolytics, and current smoker.

Study Design

Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
remifentanil / lidocaine
Remifentanil TCI group : target controlled infusion of 2.0ng/ml of remifentanil on end of surgery. Lidocaine IV group : Intravenous administration of 1.5mg/kg of lidocaine on end of surgery.

Locations

Country Name City State
Korea, Republic of Severance Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of lidocaine and remifentanil for the effect on responses to the endotracheal tube during emergence from general anesthesia The incidence and the grade of cough during emergence from general anensthesia between remifentanil TCI group and lidocaine IV administration group. No
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