Femoral and Epidural Block After Total Knee Arthroplasty

NCT02115945 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-04-16

No results posted yet for this study

Summary

Total knee prosthetic replacement causes severe postoperative pain. Various analgesic techniques have been used in pain control. Comparison of epidural and femoral nerve block is lacking, furthermore effect on chronic pain is unclear. The investigators aimed to compare the effects of epidural and femoral block on acute and chronic postoperative pain.

Conditions

  • Acute Postoperative Pain
  • Chronic Postoperative Pain

Interventions

OTHER

DN4 test

The DN4 test was used to evaluate neuropathic pain.

OTHER

The SF 12 test

The SF 12 test (SHORT FORM 12) was used to evaluate quality of life.

OTHER

HAD scale

The anxiety/depression scale (HAD) was used to assess anxiety and depression.

OTHER

Visual analogue score

Visual analogue score vas used to evaluate pain.

PROCEDURE

femoral block

PROCEDURE

epidural block

Sponsors & Collaborators

  • Aydin Adnan Menderes University

    lead OTHER

Principal Investigators

  • Sinem Sari, Assistant Prof · Adnan Menderes University Medical Faculty Anesthesiology and Reanimation Department

  • Fatma Şengül, MD · Antalya Education and Research Hospital, Anesthesiology and Reanimation Department, Antalya; Turkey

  • FabrizioGalimberti Galimberti, Medical Student · Cleveland ClinicLernerCollege of Medicine, Cleveland, Ohio

  • Bilge Karslı, Prof · Antalya Education and Research Hospital, Anesthesiology and Reanimation Department, Antalya; Turkey

  • Alparslan Turan, Associate Prof · Department of Outcomes Research, Cleveland Clinic

  • Murat Bakıs, Assistant Prof · Adnan Menderes University Medical Faculty, Anesthesiology and Reanimation Department, Aydin; Turkey

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2014-03-31
Completion
2014-03-31

Countries

  • Turkey (Türkiye)

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 NCT02115945 on ClinicalTrials.gov