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The Effect of Popliteal Plexus Block on Pain After Total Knee Arthroplasty

NCT03198403 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2017-09-29

No results posted yet for this study

Summary

The study aims to investigate the effect of the Popliteal plexus block (PPB) on postoperative pain after total knee arthroplasty

Conditions

  • Popliteal Plexus Block
  • Total Knee Arthroplasty

Interventions

DRUG

Bupivacaine-epinephrine

Popliteal plexus block with 10 mL of bupivacaine-epinephrine 5 mg/mL + 5 microgram/mL.

Sponsors & Collaborators

  • Regionshospitalet Silkeborg

    lead OTHER

Principal Investigators

  • Charlotte Runge, MD · University of Aarhus

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-01
Primary Completion
2017-09-26
Completion
2017-09-28

Countries

  • Denmark

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 NCT03198403 on ClinicalTrials.gov