Overview

Levobupivacaine and Postoperative Pain Relief

Status:
Completed
Trial end date:
2013-12-01
Target enrollment:
0
Participant gender:
All
Summary
The study analysed direct levobupivacaine instillation in surgical wound and its effectiveness in postoperative pain control. Half participants received 0,5 % levobupivacaine and the other half received 0,9% saline solution
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Institute for Mother and Child Health Care of Serbia "Dr Vukan Cupic"
Treatments:
Acetaminophen
Analgesics
Ibuprofen
Levobupivacaine
Criteria
Inclusion Criteria:

- elective surgery

- not having incarcerated hernia

- not having previous surgeries requiring general anaesthesia American Society of
Anesthesia scores I and II

- not having allergy to topical anesthetics, paracetamol, ibuprofen and/or general
anesthetics, opioids or muscle relaxants

Exclusion Criteria:

- worsening of health status prior to surgery

- parental withdrawal to study