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NCT05960253 Clinical Trial

Peroperative Effect of Regional Anesthesia in Hip Surgery

Analgesia Clinical Trial

Official title:
Comparison of the Peroperative Efficacy of Pericapsular Nerve Group Block and Lumbar Erector Spina Plan Block Applied Preoperatively in Patients Undergoing Hip Fracture Operation

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05960253
Other study ID # hip surgery
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 20, 2023
Est. completion date December 1, 2023

Study information
Verified date November 2023
Source Ankara City Hospital Bilkent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A total of 120 patients scheduled for surgical operation due to hip fracture were divided into two randomized groups. The first group received pericapsular nerve group (PENG) block, while the second group received lumbar erector spinae plane (L-ESP) block prior to the surgery. Subsequently, all patients were positioned in the lateral decubitus position before spinal anesthesia and compared in terms of anesthesia effectiveness through pain scores.

Recruitment information / eligibility
Status Recruiting
Enrollment 120
Est. completion date December 1, 2023
Est. primary completion date September 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - American Society of Anesthesiologists(ASA) 2-3 patients undergoing surgery due to hip fracture. Exclusion Criteria: - Patients in whom regional anesthesia is contraindicated. - Patients who are unable to communicate. - Patients with a known allergy to local anesthetics. - Patients with organ failure.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Pericapsular Nerve Group Block
1st group to be applied PENG block
• Lumber Erector Spinae Plane Block
2nd group to be applied Lumber ESP block

Locations
Country Name City State
Turkey Ankara City Hospital Ankara

Sponsors (1)
Lead Sponsor Collaborator
Ankara City Hospital Bilkent

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Analgesia Pain measurement via Visual Analog Scale (VAS) scores 30 minutes
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