The purpose of this study is to monitor whether preicncisional bupivacaine (bupivacaïne 0,5% with epinefrine 1:200.000), infiltration in trocarcincisions reduces postoperative wound pain.
ID
Source
Brief title
Condition
- Other condition
- Therapeutic and nontherapeutic effects (excl toxicity)
- Soft tissue therapeutic procedures
Synonym
Health condition
pijnbeleving
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
reduction in postoperative wound pain (VAS score)
Secondary outcome
woundinfection
Background summary
Preincisional bupivacaine infiltration seems to be effective in postoperative
painreduction in tonsillectomy, appendectomy, gynecologic and orthopedic
procedures.
Study objective
The purpose of this study is to monitor whether preicncisional bupivacaine
(bupivacaïne 0,5% with epinefrine 1:200.000), infiltration in trocarcincisions
reduces postoperative wound pain.
Study design
Double blind randomisation in two groups: 1 (bupivacaïne group) and 2 placebo
group).
Study burden and risks
questionnary (max half an hour)
Montessoriweg 1
3083 AN Rotterdam
Nederland
Montessoriweg 1
3083 AN Rotterdam
Nederland
Listed location countries
Age
Inclusion criteria
all patients
Exclusion criteria
ASA III/IV
age under 18 yrs
bupivacaine allergy
peroperative conversion
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| CCMO | NL14477.101.06 |