MedTrace Logo

Study of Transdermal Fentanyl Patch to Treat Postoperative Pain in Total Knee Arthroplasty

NCT01348984 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2011-05-06

No results posted yet for this study

Summary

The purpose of this study is to determine whether transdermal fentanyl patch

Conditions

  • Postoperative Pain

Interventions

DRUG

transdermal fentanyl patch

TFP = transdermal fentanyl patch (50 microgram/hour)

DRUG

placebo patch

group 2 = placebo patch

Sponsors & Collaborators

  • Khon Kaen University

    lead OTHER

Principal Investigators

  • Thepakorn Sathitkarnmanee, MD · Faculty of Medicine, Khon Kaen University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2010-10-31
Completion
2010-12-31

Countries

  • Thailand

Study Locations

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 NCT01348984 on ClinicalTrials.gov