MedTrace Logo

Continuous Bupivacaine Infusion Following Colonic Surgery

NCT00557843 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-05-21

No results posted yet for this study

Summary

The primary objective is to evaluate the influence of continuous local anesthetic infiltration on tissue oxygenation after surgical procedures requiring abdominal surgery as a major predictor for wound healing.

Conditions

  • Abdominal Surgery

Interventions

DRUG

Bupivacaine

Wound perfusion with bupivacaine, plus patient controlled analgesia (PCA)

DRUG

Saline

Wound perfusion with placebo solution (isotonic saline) plus patient controlled analgesia (PCA)

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Andrea Kurz, MD · The Cleveland Clinic

  • Daniel I Sessler, MD · The Cleveland Clinic

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2009-06-30
Completion
2009-06-30

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00557843 on ClinicalTrials.gov