Pre-incisional bupivacaine infiltration trocarincions, reduction of postoperative pain?

Phase 3

Completed

• Conditions: pijnbeleving; incisional pain; 10062915; 10041297

• Registration Number: NL-OMON30342
• Lead Sponsor: Ikazia Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

all patients

Exclusion Criteria

ASA III/IV
age under 18 yrs
bupivacaine allergy
peroperative conversion

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>reduction in postoperative wound pain (VAS score)</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>woundinfection</p><br>