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Pain Control of Thoracoscopic Major Pulmonary Resection

NCT01758809 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2013-01-01

No results posted yet for this study

Summary

The purpose of this study is to evaluate whether pre-emptive local bupivacaine injection is a better alternative pain control modality than the conventional intravenous patient controlled analgesia.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

Pre-emptive bupivacaine wound infiltration

Pre-emptive bupivacaine wound infiltration

PROCEDURE

intravenous patient controlled analgesia

postoperative pain control with intravenous patient controlled analgesia

Sponsors & Collaborators

  • Seoul National University Bundang Hospital

    lead OTHER

Principal Investigators

  • Sanghoon Jheon, M.D., Ph.D. · Seoul National University Bundang Hospital

  • Hee Chul Yang, M.D. · Seoul National University Bundang Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2011-09-30
Completion
2011-11-30

Countries

  • South Korea

Study Locations

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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 NCT01758809 on ClinicalTrials.gov