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Effect of Local Infiltration Anesthesia With Ropivacaine on Pain After Primary Total Hip Arthroplasty

Not Applicable
Completed
Conditions
Osteoarthritis, Hip
Interventions
Procedure: local infiltration anesthesia using saline
Procedure: local infiltration anesthesia using Ropivacaine and Epinephrine
Procedure: Multimodal analgesic regimen
Registration Number
NCT02359136
Lead Sponsor
St. Olavs Hospital
Brief Summary

Background: The Local infiltration analgesic (LIA) technique has been widely used to reduce opioid requirements and improve the patient's mobilization after total hip arthroplasty (THA). However, the evidence for LIA in THA remains to be clarified.

Purpose: To evaluate whether a single shot LIA in addition to a multimodal analgesic regimen reduces acute postoperative pain and opioid requirements after THA.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
116
Inclusion Criteria
  • all patients receiving total hip arthroplasty in the study period
Exclusion Criteria
  • contraindications to receive spinal anesthetic, Dexamethasone or Acetaminophen.
  • Patients who received general anaesthetic
  • patients who will get a different operation than standard direct lateral surgery
  • Patients with osteosynthesis to be removed in the same operation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
LIA placebolocal infiltration anesthesia using salinelocal infiltration anesthesia using saline i addition to multimodal analgesic regimen
LIA RopivacaineMultimodal analgesic regimenlocal infiltration anesthesia using Ropivacaine and Epinephrine i addition to multimodal analgesic regimen
LIA Ropivacainelocal infiltration anesthesia using Ropivacaine and Epinephrinelocal infiltration anesthesia using Ropivacaine and Epinephrine i addition to multimodal analgesic regimen
LIA placeboMultimodal analgesic regimenlocal infiltration anesthesia using saline i addition to multimodal analgesic regimen
Primary Outcome Measures
NameTimeMethod
postoperative pain assessed by numeric rating scale1 day (first postoperative day)

assessed by numeric rating scale

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

St.Olavs Hospital, Department of Orthopedics

🇳🇴

Trondheim, Norway

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