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Effect of a Lateral Nerve of the Thigh Block on Postoperative Pain After Total Hip Replacement Surgery

NCT02289937 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2014-11-13

No results posted yet for this study

Summary

The purpose of this study was to evaluate the analgesic efficacy of the nervus cutaneous femoral lateralis (NCFL) blockade on postoperative pain after total hip replacement surgery. The NCFL-block is a pure sensory block. We hypothesized that the NCFL-block would reduced the postoperative pain without delaying mobilization.

Conditions

  • Pain, Postoperative
  • Anesthesia, Conduction
  • Arthroplasty, Replacement, Hip

Interventions

DRUG

Ropivacaine

DRUG

Placebo

DEVICE

An ultrasound-guided Nervus cutaneous femoral lateralis blockade will be given postoperatively

Sponsors & Collaborators

  • Daniel Hägi-Pedersen

    lead OTHER

Principal Investigators

  • Daniel Hägi-Pedersen, M.D., Ph.D. · Naestved Hospital, Department of Anaesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2014-10-31
Completion
2014-10-31

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Entities

Drugs

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 NCT02289937 on ClinicalTrials.gov