Peroperative Effect of Regional Anesthesia in Hip Surgery
Comparison of the Peroperative Efficacy of Pericapsular Nerve Group Block and Lumbar Erector Spina Plan Block Applied Preoperatively in Patients Undergoing Hip Fracture Operation
1 other identifier
interventional
120
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 18, 2023
CompletedFirst Posted
Study publicly available on registry
July 25, 2023
CompletedStudy Start
First participant enrolled
August 20, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2023
CompletedNovember 28, 2023
November 1, 2023
12 days
July 18, 2023
November 26, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Analgesia
Pain measurement via Visual Analog Scale (VAS) scores
30 minutes
Study Arms (2)
PENG block group
ACTIVE COMPARATORL-ESP group
EXPERIMENTALInterventions
Eligibility Criteria
You may qualify if:
- \- American Society of Anesthesiologists(ASA) 2-3 patients undergoing surgery due to hip fracture.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara City Hospital
Ankara, 06800, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor Doctor
Study Record Dates
First Submitted
July 18, 2023
First Posted
July 25, 2023
Study Start
August 20, 2023
Primary Completion
September 1, 2023
Study Completion
December 1, 2023
Last Updated
November 28, 2023
Record last verified: 2023-11