Status:

TERMINATED

Femoral Nerve Block With Bupivacaine and Adjuvant Dexamethasone in Patients With Hip Fracture

Lead Sponsor:

University of Aarhus

Conditions:

Hip Fracture

Eligibility:

All Genders

55+ years

Phase:

PHASE4

Brief Summary

Prolongation of the analgesic effect of a femoral nerve block from the present 15 hours to 24 hours in patients with hip fracture would have a major impact in order to provide better preoperative anal...

Detailed Description

Patients with hip fractures are most often old, have multiple comorbidities and suffer severe pain. Femoral nerve block as a means of preoperative analgesia for these patients has proven effective in...

Eligibility Criteria

Inclusion

  • Clinical suspicion of hip fracture
  • Age ≥ 55 years
  • Mentally capable of comprehending and using verbal pain score
  • Mentally capable of differentiating between pain from the fractured hip and pain from other locations
  • Mentally capable of understanding the given information
  • Arrival in the emergency room at times when one of the doctors who do the nerve blocks for this investigation are on call
  • Verbal pain score (0-10) ≥ 7 with passive leg raise of the fractured leg at the time of inclusion
  • Patients informed consent

Exclusion

  • Hip fracture not confirmed by x-ray
  • Weight \< 40 kg
  • Verbal pain score \> 3, 30 minutes after the nerve block
  • Verbal pain score \> 5 with passive leg raise, 30 minutes after the nerve block
  • Patient has previously been included in this trial
  • Ongoing pre traumatic treatment with parenteral or intravenous adrenocortical hormone
  • Verbal pain score \> 3 from other locations than the fractured hip
  • If the patient wishes to be excluded
  • Allergy to local anesthetics or adrenocortical hormone
  • Visible infection in the area of the point of needle injection
  • Acute inability to comprehend and use verbal pain score

Key Trial Info

Start Date :

March 1 2015

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2015

Estimated Enrollment :

7 Patients enrolled

Trial Details

Trial ID

NCT02248870

Start Date

March 1 2015

End Date

September 1 2015

Last Update

September 14 2015

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Aarhus University Hospital

Aarhus, Aarhus, Denmark, 8000