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Clinical Trials/NCT06088368
NCT06088368
Not yet recruiting
Not Applicable

Investigation of the Efficacy of Different Types of Lumbar Plexus Block Applied With Ultrasound-guided Shamrock Method

Bursa Yüksek İhtisas Education and Research Hospital1 site in 1 country40 target enrollmentOctober 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Femoral Neck Fractures
Sponsor
Bursa Yüksek İhtisas Education and Research Hospital
Enrollment
40
Locations
1
Primary Endpoint
Block application time
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The more effective use of ultrasound in regional anaesthesia techniques has made different block applications possible. Lumbar plexus block is also used for post-operative analgesia and surgical anaesthesia. Currently, in-plane ultrasound-guided LPB is widely used in short-axis imaging and Shamrock imaging.

Detailed Description

The purpose of this use is to investigate the effectiveness of lumbar plexus block application applied with in-plane and out-of-plane methods accompanied by Shamrock imaging.

Registry
clinicaltrials.gov
Start Date
October 20, 2023
End Date
February 13, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bursa Yüksek İhtisas Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Korgün Ökmen

Principal Investigator

Bursa Yüksek İhtisas Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • 18-90 years old
  • ASA (American Society of Anaesthesiologist) Score I-III risk class
  • Patients who will undergo femoral neck fracture operation.

Exclusion Criteria

  • Local Anaesthetic Allergy
  • With Bleeding Diathesis Disorder
  • Mental Disorders
  • Allergic to the medicines used
  • Previous Cerebrovascular Disease
  • Body Mass Index above 30

Outcomes

Primary Outcomes

Block application time

Time Frame: up to 20 minutes

The stopwatch will be started by another researcher with the needle skin penetration and the stopwatch will be stopped as soon as the needle leaves the skin.

Secondary Outcomes

  • sensory block(up to 40 minutes)
  • Number of interventions(up to 20 minutes)
  • motor block(up to 40 minutes)
  • The number of needle guidance(up to 20 minutes)

Study Sites (1)

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