Overview

Perioperative Lidocaine Administration in Thoracoscopic Surgery for Improved Postoperative Pain Control

Status:
Recruiting
Trial end date:
2022-12-01
Target enrollment:
0
Participant gender:
All
Summary
Placebo-controlled study to analyze the effect of perioperative intravenous lidocaine administration on total morphine consumption (TMC) and on pain intensity in thoracoscopic surgery .
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Hospital, Basel, Switzerland
Treatments:
Lidocaine
Criteria
Inclusion Criteria:

- Patients undergoing video-assisted thoracoscopic procedures under general anaesthesia.

- American Society of Anesthesiologists (ASA) physical Status classes I to III

- age ≥ 18 years

- Patient informed consent

Exclusion Criteria:

- Contraindications to the class of drugs under study, e.g. known hypersensitivity or
allergy to class of drugs or the investigational product

- Contraindications to self-administration of opioids

- Women who are pregnant or breast feeding

- Steroid therapy

- Chronic pain therapy

- Atrioventricular block grade II to III

- Congestive heart failure

- Liver insufficiency

- Known or suspected non-compliance, drug or alcohol abuse

- Inability to follow the procedures of the study, e.g. due to language problems,
psychological disorders, dementia

- Participation in another study with investigational drug within the 30 days preceding
and during the present study,

- Enrolment of the investigator, his/her family members, employees and other dependent
persons