MORphine use in the Fascia Iliaca Compartment block with UltraSound

Phase 4

Completed

• Conditions: Regionale Pijnstilling; Injection with painmedication to obtain anesthesia of the hip; 10005942

• Registration Number: NL-OMON47062
• Lead Sponsor: Zuyderland Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

Adult patient diagnosed with a proximal femur fracture upon arrival at the ED.

Exclusion Criteria

No informed consent patient;Skin infection at injection site(s);Morphine allergy;Levobupivacaine allergy;Operation within an hour after admission;Inability to understand and quantify pain on a NRS;Dementia;Neurological deficit of fractured leg upon arrival at the ED;Trauma with multiple fractures (more than 1);Risk of compartment syndrome of ipsilateral lower leg.;Proximal femur fracture with other definitive treatment than operation;Transfer to another hospital;Actual morphine use;Distracting pain in other location than hip;Pregnancy;No physician/nurse available for procedure.;BMI > 40;Saturation < 90%

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study endpoint will be the mean preoperative morphine use between the<br /><br>groups. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary parameters will include the pain scores reported by the numerical<br /><br>rating scale both at rest and during transport to another bed and side effects<br /><br>from morfine are compared.</p><br>