Overview
Levobupivacaine and Postoperative Pain Relief
Status:
Completed
Completed
Trial end date:
2013-12-01
2013-12-01
Target enrollment:
0
0
Participant gender:
All
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 solutionPhase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
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