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

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Yonsei University

Status

Terminated

Conditions

Asymptomatic Gallstones Without Cholecystitis
Gallbladder Polyp

Treatments

Drug: Dexamethasone
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT02224170
4-2014-0530

Details and patient eligibility

About

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

Enrollment

8 patients

Sex

All

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-II patients aged between 20 and 65 year undergoing laparoscopic cholecystectomy due to gallbladder polyp or asymptomatic gallstones without cholecystitis

Exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

8 participants in 2 patient groups

Lidocaine group
Experimental group
Treatment:
Drug: Lidocaine
Dexamethasone group
Active Comparator group
Treatment:
Drug: Dexamethasone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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