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Intra-operative Lidocaine Infusion in Preventing CPSP Post VATs

Unknown statusPhase 4NCT02862769
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

The aim of this study is to evaluate the impact of intravenous lidocaine on acute and chronic post surgical pain on patients undergoing video assisted thoracoscopic surgery(VATS). The investigators believe that systemic administration of lidocaine during the perioperative period would be effective in preventing chronic pain post VATS. In addition to chronic pain the investigators believe it will reduce acute postoperative pain as well as each patients total opioid requirement.The investigators believe that this will have a significant impact on the care of patients presenting for VATS.

Study details

Official title
The Role of Intra-operative Lidocaine Infusion in Preventing Chronic Post Surgical Pain After Video Assisted Thoracoscopic Surgery
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Start date
2017-01-01
Primary completion
2019-12
Sex
All
Age range
from 18 Years to 75 Years
Results posted
No results posted in this snapshot
Countries
Canada
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * VATs for lobectomy * Understanding of English (reading, writing and speaking) * Written consent for being involved in this study * Exclusion Criteria: * Chronic pain including fibromyalgia * Patients using opioids (more than 80 mg equivalent of oral morphine/day for \>60 days) * Major depression * Received or going to receive chemotherapy or radiotherapy. * Pregnant

Canadian sites (1)

FacilityCityProvince
London Health Sciences CentreLondonOntario

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02862769