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Obturator and Femoral Nerve Block in Patients With Hip Fracture

13 maj 2016 uppdaterad av: University of Aarhus

Analgesic Effect of an Obturator Nerve Block Combined With a Femoral Nerve Block Compared With Femoral Nerve Block Alone in Patients With Hip Fracture

A higher number than expected of patients with hip fracture have only insufficient analgesic effect of a femoral nerve block, which is the nerve block commonly used for this group of patients. One of the possible causes of this failure to provide analgesia from a single nerve block could be the that other nerves are involved in transmitting the pain signal. One of the nerves that is believed to give off branches to the hip is the obturator nerve.

With ultrasound it is possible to make a selective proximal nerve block of the obturator nerve.

The aim of this trial is to test the analgesic effect of a femoral nerve block i combination with an obturator nerve block compared to femoral nerve block alone in a randomized and placebo controlled design.

Studieöversikt

Status

Okänd

Betingelser

Detaljerad beskrivning

A higher number than expected of all patients with hip fracture have only insufficient analgesic effect of a femoral nerve block. One of the possible causes of this failure to provide analgesia from a single nerve block could be the that other nerves are involved in transmitting the pain signal. One of the nerves that is believed to give off branches to the hip is the obturator nerve. Earlier it was believed that the so called '3-in-1-block' or the iliac fascia compartment block would anesthetize also the obturator nerve, and these two nerve blocks have been uses extensively in the emergency ward for preoperative analgesia. Today that is not believed to be true and consequently is the part of the obturator nerve in patients with hip fracture unknown.

With ultrasound it is possible to make a selective proximal nerve block of the obturator nerve before it branches into an anterior and a posterior branch. A selective nerve block of the obturator nerve to access its effect in patients with hip fracture has to our knowledge never been done.

The aim of this trial is to test the analgesic effect of a femoral nerve block i combination with an obturator nerve block compared to femoral nerve block alone in a randomized and placebo controlled design.

Studietyp

Interventionell

Inskrivning (Förväntat)

90

Fas

  • Fas 4

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Aarhus, Danmark, 8000
        • Rekrytering
        • Aarhus University Hospital
        • Kontakt:
        • Kontakt:
          • Thomas F. Bendtsen, MD, Ph.d.
          • Telefonnummer: +45 51542997
          • E-post: tfb@dadlnet.dk

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

55 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • 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 numeric pain scale score (NRS 0-10) > 5 with a dynamic test OR NRS > 3 at rest
  • Patients informed consent

Exclusion Criteria:

  • Hip fracture not confirmed by x-ray
  • Weight < 40 kg
  • Patient has previously been included in this trial
  • 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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Bupivacaine
Obturator nerve block
Obturator nerve block
Andra namn:
  • Active nerve block
Placebo-jämförare: Saline
Saline is injected as a placebo
Obturator nerve block with saline(placebo)
Andra namn:
  • Placebo

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Success rate of successful analgesia, measured with numeric rating scale(NRS) 0-10 with 0=no pain and 10=worst pain. Successful analgesia = NRS<4 at rest and NRS <6 with passive movement of the fractured leg.
Tidsram: 30 minutes
Success rate of successful analgesia compared between the groups
30 minutes

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Median pain score (NRS 0-10)
Tidsram: 30 minutes
Median pain score 30 minutes after the nerve blocks compared between the groups
30 minutes
Median change in pain score (NRS 0-10)
Tidsram: 30 minutes
Median change in pain score 30 minutes after the nerve blocks compared between the groups
30 minutes
Course in pain reduction
Tidsram: 30 minutes
Course in pain reduction during the 30 minutes after the nerve blocks
30 minutes
Time to sufficient analgesia
Tidsram: 30 minutes
Time from ended injection until sufficient analgesia
30 minutes
Frequency of anesthesia in the skin area of the saphenous nerve
Tidsram: 30 minutes
Frequency of anesthesia in the skin area innervated by the saphenous nerve
30 minutes
Frequency of anesthesia in the skin area of the anterior cutaneous branches of the femoral nerve
Tidsram: 30 minutes
Frequency of anesthesia in the skin area of the anterior cutaneous branches of the femoral nerve
30 minutes
Localization of the worst pain before block
Tidsram: 0 minutes
Localization of the worst pain before any nerve blocks
0 minutes
Localization of the worst pain after block
Tidsram: 30 minutes
Localization of the worst pain 30 minutes after the nerve blocks
30 minutes
Discomfort during nerve block procedures (score 0-10, 0=no discomfort)
Tidsram: 5 minutes
Discomfort during the nerve block procedures compared between procedures
5 minutes
Satisfaction (0-10, 0= very unsatisfactory)
Tidsram: 30 minutes
Patient satisfaction with the pain treatment
30 minutes
Frequency of ultrasound visualization of femoral nerve
Tidsram: 5 minutes
Frequency of patients with possible ultrasound visualization af the femoral nerve
5 minutes
Frequency of ultrasound visualization of obturator injection site
Tidsram: 5 minutes
Frequency of patients with possible ultrasound visualization of the obturator nerve block injection site
5 minutes
Time spend on femoral nerve block
Tidsram: 5 minutes
Time spend on conducting the femoral nerve block
5 minutes
Time spend on obturator nerve block
Tidsram: 5 minutes
Time spend on conducting the obturator nerve block
5 minutes
Total morphine equivalent dose of opioid from the time of nerve block to operation
Tidsram: Approximately 24 hours in average
Total morphine equivalent dose of opioid from the time of nerve block until the time of operation
Approximately 24 hours in average
Total morphine equivalent dose of opioid/time from the time of nerve block to operation
Tidsram: Approximately 24 hours in average
Total morphine equivalent dose of opioid/time from the time of nerve block until the time of operation
Approximately 24 hours in average
Total morphine equivalent dose of opioid in the first 10 hours after nerve block
Tidsram: 10 hours
Total morphine equivalent dose of opioid given in the first 10 hours after nerve block
10 hours
Total morphine equivalent dose of opioid/time in the first 10 hours after nerve block
Tidsram: 10 hours
Total morphine equivalent dose of opioid/time given in the first 10 hours after nerve block
10 hours

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Studierektor: Thomas F. Bendtsen, Ph.d., Aarhus University Hospital

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 oktober 2015

Primärt slutförande (Förväntat)

1 april 2017

Avslutad studie (Förväntat)

1 april 2017

Studieregistreringsdatum

Först inskickad

27 augusti 2015

Först inskickad som uppfyllde QC-kriterierna

1 september 2015

Första postat (Uppskatta)

4 september 2015

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

16 maj 2016

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

13 maj 2016

Senast verifierad

1 maj 2016

Mer information

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