Clinical Trials Directory

Trials / Terminated

TerminatedNCT02224170

Comparison of Effect on Quality of Recovery Outcome Between Systemic Lidocaine and Dexamethasone in Patients Undergoing Laparoscopic Cholecystectomy

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this study is to compare the effect of lidocaine and dexamethasone on postoperative quality of recovery after laparoscopic cholecystectomy

Conditions

Interventions

TypeNameDescription
DRUGLidocaineLidocaine 2mg Kg-1 in normal saline (total volume 25mL) was infused after tracheal intubation, and lidocaine was infused at the rate of lidocaine 2mg Kg-1 h-1 (0.2 ml Kg-1 h-1, equivalent volume as normal saline in dexamethasone group) until the end of surgery (at the time of skin closure).
DRUGDexamethasoneDexamethasone 8mg in normal saline (total volume 25mL) was infused after tracheal intubation, and normal saline was continuously infused at the rate of 0.2 ml Kg-1 h-1 until the end of surgery (at the time of skin closure).

Timeline

Start date
2014-11-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2014-08-25
Last updated
2019-03-19

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02224170. Inclusion in this directory is not an endorsement.