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NCT Number: NCT06631118

Pericapsular Nerve Block Versus Propofol During Hip Fractures Surgery

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.

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Key information

Conditions

Difference in Reduction in Visual Analogue Score at 30 Minutes

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

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

Procedure

Patients in group A will receive ultrasound guided pericapsular nerve group block (PENG) while patients in group B will receive low dose intravenous Propofol0.7mg/kg] over 30 seconds followed by spinal anesthesia in both groups

Primary outcomes

  1. The difference in VAS scale

    Time frame: 30 min after giving propofol and the PENG block.

    The primary outcome will be difference in median reduction in VAS-D .

Study contacts

Contact information is provided by the study sponsor or research team.

Marwa Mamdouh Mohamed

CONTACT

[email protected]

01000205686 ext. 002

Mohamed Mourad Ali

CONTACT

[email protected]

01006512101 ext. 002

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Pericapsular Nerve Group (PENG) Block Versus Low Dose Propofol to Achieve Painless Sitting Position Before Spinal Anesthesia in Patients With Hip Fractures

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 8, 2024
Registry last updated
Oct 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.