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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-06

Study Completion Date

2021-07-05

Brief Summary

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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.

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Detailed Description

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Conditions

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Pain, Acute

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Randomization of the study will be done by a doctor who will not participate in patient follow-up with closed envelopes using computer generated randomization codes.

Study Groups

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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.

Group Type ACTIVE_COMPARATOR

PENG Block

Intervention Type PROCEDURE

Pericapsular Nerve Group Block

Control

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

Group Type ACTIVE_COMPARATOR

Conventional opioid analgesia (Fentanyl)

Intervention Type DRUG

standardised intravenous opioid

Interventions

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PENG Block

Pericapsular Nerve Group Block

Intervention Type PROCEDURE

Conventional opioid analgesia (Fentanyl)

standardised intravenous opioid

Intervention Type DRUG

Eligibility Criteria

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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

Minimum Eligible Age

35 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No