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Pericapsular Nerve Block Versus Propofol During Hip Fractures Surgery

A

Ain Shams University

Status

Not yet enrolling

Conditions

Difference in Reduction in Visual Analogue Score at 30 Minutes

Treatments

Procedure: pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B

Study type

Interventional

Funder types

Other

Identifiers

NCT06631118
FMASU R 130/2024

Details and patient eligibility

About

The study will compare the efficacy of Pericapsular nerve group block (PENG) versus low dose Propofol for the achievement of painless sitting position before spinal anesthesia in patients undergoing repair of Hip fractures.

Enrollment

60 estimated patients

Sex

All

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients in the age group ranging 40-70, both genders, belonging to physical status American Society of Anaesthesiologists (ASA) I and II

Exclusion criteria

  • Patients with old fractures (more than 7 days), polytrauma, bleeding disorders or coagulopathy, local site infection, difficulty expressing pain scores such as hearing disability, mentally challenged, dementia or psychiatric illness and who refused to take part

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Group A
Active Comparator group
Description:
Group (A ) : will receive ultrasound guided pericapsular nerve group block (PENG) followed by spinal anesthesia.
Treatment:
Procedure: pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B
Group B
Active Comparator group
Description:
Group B will receive low dose intravenous Propofol \[0.7mg/kg\] over 30 seconds followed by spinal anesthesia and so far, this is the most common and standard technique to achieve sitting position during spinal anesthesia for patients with hip fractures.
Treatment:
Procedure: pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B

Trial contacts and locations

0

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Central trial contact

Mohamed Mourad Ali; Marwa Mamdouh Mohamed

Data sourced from clinicaltrials.gov

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