ClinicalTrials.Veeva

Menu

Effect of Perioperative Intravenous Lidocaine Infusion on Postoperative Recovery in Patients Undergoing Arthroscopic Rotator Cuff Repair Under General Anesthesia

Yonsei University logo

Yonsei University

Status

Completed

Conditions

Rotator Cuff Tears

Treatments

Drug: Lidocaine
Drug: Normal saline

Study type

Interventional

Funder types

Other

Identifiers

NCT04061057
4-2018-0033

Details and patient eligibility

About

Arthroscopic rotator cuff repair is a commonly performed procedure but is known to cause significant postoperative pain. Effective analgesia after rotator cuff repair is crucial in improving the well-being of the patient but also to ensure long-term rehabilitation. The most commonly used analgesic for acute postoperative pain is opioids. However, the use of opioids is accompanied by several side effects which include but are not limited to nausea/vomiting, urinary retention, itching sensation and sometimes dizziness, respiratory depression and hypotension in higher doses. As of late, many efforts are aimed toward decreasing the use of opioids by using multimodal analgesia. Among such methods, intravenous lidocaine has been reported to be effective, safe and economic in various procedures. However, the existing evidence is mostly focused on laparoscopic procedures. The present study aims to find whether perioperative infusion of lidocaine is able to decrease opioid requirements after surgery and also improve postoperative pain compared to placebo in patients undergoing arthroscopic rotator cuff repair.

Enrollment

98 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ASA class 1-3 adults over 19 years scheduled for elective arthroscopic rotator cuff repair

Exclusion criteria

  1. Known allergies to lidocaine or propofol
  2. Cardia arrhythmia
  3. History of epilepsy or seizures
  4. Liver/kidney failure
  5. History of recent strong opioid use

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

98 participants in 2 patient groups, including a placebo group

IV lidocaine
Experimental group
Description:
Perioperative IV lidocaine infusion
Treatment:
Drug: Lidocaine
Normal saline
Placebo Comparator group
Description:
Perioperative IV normal saline infusion
Treatment:
Drug: Normal saline

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems