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Effect of Local Infiltration Anesthesia With Ropivacaine on Postoperative Pain After Hip Hemiarthroplasty

Effect of Local Infiltration Anesthesia With Ropivacaine on Postoperative Pain After Hip Hemiarthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02585011
Enrollment
123
Registered
2015-10-23
Start date
2015-12-31
Completion date
2018-05-13
Last updated
2020-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Femoral Neck Fractures

Keywords

Hemiarthroplasty, Anesthesia, Local, Pain, Postoperative

Brief summary

At St.Olavs Hospital each year about 400 patients are treated for femoral neck fractures, 250 of them receiving hemiarthroplasty. Implementation of fast-track clinical pathways reduces morbidity and enhances recovery of patients undergoing hemiarthroplasty. One of the key prerequisites for early rehabilitation is optimized pain relief. Local infiltration anesthesia with Ropivacaine is part of a multimodal pain regimen for patients receiving hemiarthroplasty at St.Olavs Hospital, although the pain reducing effect of local Ropivacaine after hemiarthroplasty has not been investigated in clinical trials. In this study it will be investigated whether a single shot with Ropivacaine reduces acute postoperative pain and opioid requirement after hemiarthroplasty. The findings of this study will have a direct impact on patient treatment.

Interventions

DRUGRopivacaine
DRUGEpinephrine
DRUGSaline

Sponsors

Norwegian University of Science and Technology
CollaboratorOTHER
St. Olavs Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* scheduled for hemiarthroplasty at St. Olavs Hospital * competent and willing to give consent * able to be mobilized in the PACU and in the trauma ward unit.

Exclusion criteria

* contraindications for spinal anesthesia, Dexamethasone, Dolcontin or Acetaminophene * receiving general anesthesia * patients operated on with an approach different to standard direct lateral surgery * receiving osteosyntheses * receiving femoral block less than 4 hours before surgery

Design outcomes

Primary

MeasureTime frameDescription
Pain sensation during mobilization in the post-anesthesia care unit.24 hours (day of surgery)Pain is registered using the numeric rating scale (NRS) by the nurses both during rest and mobilization. The patients are asked a standard question; on a scale from 0 to 10, where 0 is no pain and 10 is the worst imaginable pain, can you define the pain you have right now?

Secondary

MeasureTime frameDescription
Pain during mobilization on the day after surgery48 hours (first postoperative day)Pain is registered using the numeric rating scale (NRS) by the nurses both during rest and mobilization. The patients are asked a standard question; on a scale from 0 to 10, where 0 is no pain and 10 is the worst imaginable pain, can you define the pain you have right now?
Total consumption of opioids on the first postoperative day48 hrs (first postoperative day)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026