Clinical Trials Directory

Trials / Completed

CompletedNCT02869841

Efficacy of Rectal Sheath Analgesia After Midline Laparotomy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
57 (actual)
Sponsor
Kuopio University Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Midline laparotomy is commonly used in emergency and elective cancer surgery and patients need effective and safe pain treatment after this type of surgery. Nowadays modern anticoagulant therapy may prevent use of central regional blocks in pain management. Therefore in the present study the efficacy and safety of rectus sheath analgesia is studied using different administration techniques. The primary aim is the efficacy of the rectus sheath analgesia measured with pain ratings and the amount rescue opioid used. Secondary aims were concentrations of local anesthetic, rescue opioid and satisfaction to analgesia method used.

Conditions

Interventions

TypeNameDescription
DRUGLevobupivacaine continuous infusionLevobupivacaine continuous infusion to rectus sheath catheters
DRUGlevobupivacaine bolus dosingLevobupivacaine bolus dosing to rectus sheath catheters
DRUGsingle bolus of levobupivacaineLevobupivacaine single dose to rectus sheath catheters
OTHERPlaceboNo rectus sheath analgesia

Timeline

Start date
2012-01-01
Primary completion
2018-07-01
Completion
2022-12-31
First posted
2016-08-17
Last updated
2023-10-27

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT02869841. Inclusion in this directory is not an endorsement.