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Clinical Trials/NCT01747122
NCT01747122
Completed
Not Applicable

A Randomised Trial of Peri-operative Nerve Block and Continuous Infusion of Local Anaesthetic Via Wound Catheter Versus Epidural in Patients Undergoing Open Liver Resection.

University of Edinburgh1 site in 1 country97 target enrollmentDecember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Open Liver Resection
Sponsor
University of Edinburgh
Enrollment
97
Locations
1
Primary Endpoint
Length of stay
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The investigators plan to compare epidurals versus wound catheters for effects on pain relief and recovery following open liver surgery.

Registry
clinicaltrials.gov
Start Date
December 2012
End Date
August 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing open hepatic resection for benign or malignant conditions.

Exclusion Criteria

  • Patients with contraindication to either epidural or wound catheter techniques.
  • Inability to give written, informed consent.
  • Jaundice (Bilirubin \> 100 μmol/L)
  • Liver resection combined with secondary surgical procedure.
  • Age \< 18 years
  • Pregnant women
  • patients on long term opiates for chronic pain

Outcomes

Primary Outcomes

Length of stay

Time Frame: Measurement made on day of discharge which is expected to be on average bewteen 5 and 10 days after surgery.

Number of days (to nearest half day) patients stay in hospital.

Secondary Outcomes

  • Central Venous Pressure(During liver transection)
  • Molecular response to surgery(Days 0, 1 and 3)
  • Operative field asessment(During liver transection)
  • Estimated Blood Loss(Intra-operative)
  • Pain Scores(Performed daily at 0900 hours. On the day of surgery pain scores will be performed at 2, 6 and 12 hours post surgery.)
  • Pringle time(Intra-operative)

Study Sites (1)

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