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
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine | Lidocaine 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). |
| DRUG | Dexamethasone | Dexamethasone 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.