Clinical Trials Directory

Trials / Completed

CompletedNCT01094106

Infiltration Analgesia After Caesarean Section

Local Infiltration Analgesia for Postoperative Pain After Caesarean Section. A Prospective, Randomised, Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
70 (actual)
Sponsor
North Karelia Central Hospital · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Infiltration of a local anesthetic into the surgical wound is a simple method to strive to control postoperative pain after surgery. In the investigators institution, this method is used quite often. However, there is a controversy regarding the analgesic efficacy. Moreover, the cost of the single use elastomeric pump used with this procedure is clearly higher than the costs of other routinely used analgesic methods. According to the investigators observations, infiltration of a local anesthetic into the surgical wound after caesarean section seems to reduce the need for rescue analgesics. However, the scientific evidence of the efficacy of this technique is weak. The investigators decided to conduct a prospective, controlled, randomised, double blind trial on this topic. The hypothesis is that wound infiltration with local anesthetic will reduce postoperative pain and opioid consumption after caesarean section without major adverse effects.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0,75%Postoperative wound infusion 2 ml/ h/ 48h
DRUGNaCl 0,9%Postoperative wound infusion 2 ml/h/48h

Timeline

Start date
2010-04-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2010-03-26
Last updated
2020-08-18
Results posted
2020-08-18

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01094106. Inclusion in this directory is not an endorsement.