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Clinical Trials/NCT04871061
NCT04871061
Completed
Not Applicable

Evaluation of Pericapsular Nerve Group Block on Positioning Pain for Spinal Anesthesia in Hip Fracture Patients

Cigli Regional Training Hospital1 site in 1 country80 target enrollmentMay 6, 2021

Overview

Phase
Not Applicable
Intervention
PENG Block
Conditions
Pain, Acute
Sponsor
Cigli Regional Training Hospital
Enrollment
80
Locations
1
Primary Endpoint
Pain scores on the Numeric Rating Scale (NRS)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to evaluate of analgesic effects of pericapsullar nerve group block which is performed preoperatively to assist positioning patients for performance of spinal anesthesia.

Registry
clinicaltrials.gov
Start Date
May 6, 2021
End Date
July 5, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Cigli Regional Training Hospital
Responsible Party
Principal Investigator
Principal Investigator

Hakan Aygün

principle investigator

Cigli Regional Training Hospital

Eligibility Criteria

Inclusion Criteria

  • hip fracture
  • aged between 35 and 90 years old

Exclusion Criteria

  • contraindications for spinal anesthesia and PENG block
  • impaired cognition or dementia
  • multiple fractures
  • any previous analgesic administration during the last 12 hours

Arms & Interventions

PENG Block

For patients with hip fracture and having hip surgery this study evaluates the analgesic effects of Pericapsular Nerve Group (PENG) block for positioning before spinal anesthesia.

Intervention: PENG Block

Control

in this group, standardised opioid doses (drug: Fentanyl) will be used for analgesia for positioning pain

Intervention: Conventional opioid analgesia (Fentanyl)

Outcomes

Primary Outcomes

Pain scores on the Numeric Rating Scale (NRS)

Time Frame: Group A: 5 minutes after intervention (intravenous opioid), Group B: 20 minutes after intervention (PENG block)

Changes in Numeric Rating Scale (NRS) at rest and on movement will be recorded at intervals. NRS is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").

Secondary Outcomes

  • Quality of patient's position(Group A: 5 minutes after intervention (intravenous opioid), Group B: 20 minutes after intervention (PENG block))
  • Duration of spinal anesthesia performance(Group A: 5 minutes after intervention (intravenous opioid), Group B: 20 minutes after intervention (PENG block))
  • Analgesic consumption(24 hours)

Study Sites (1)

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