TerminatedNot Applicable

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

Stopped: Due to difficulties in recruiting the subjects.

South Korea8 participantsStarted 2014-11

Plain-language summary

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

Who can participate

Age range20 Years – 65 Years

SexALL

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Exclusion criteria

✕. Steroid therapy or immunocompromised patients
✕. Diabetes mellitus
✕. Allergy to lidocaine or dexamethasone
✕. Severe renal dysfunction (serum creatinine more than 1.6mg/dl)
✕. Severe liver disease ( liver enzymes more than two times normal values)
✕. History of atrioventricular block
✕. Have a difficulty in understanding QoR-40 (40-item quality-of-recovery scoring system) or Korean language
✕. History of physicologic disease

What they're measuring

QoR-40 score

Timeframe: from baseline to 3 hours on the day after surgery

Trial details

NCT IDNCT02224170

SponsorYonsei University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-03

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