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

Cigli Regional Training Hospital

Status: Completed

Conditions: Pain, Acute

Treatments: Procedure: PENG Block; Drug: Conventional opioid analgesia (Fentanyl)

Study type: Interventional

Funder types: Other

Identifiers

NCT04871061

PENG55

Details and patient eligibility

About

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.

Enrollment: 80 patients

Sex: All

Ages: 35 to 90 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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80 participants in 2 patient groups

PENG Block

Active Comparator group

Description:

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.

Treatment:

Procedure: PENG Block

Control

Active Comparator group

Description:

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

Treatment:

Drug: Conventional opioid analgesia (Fentanyl)