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Pericapsular Nerve Block Versus Propofol During Hip Fractures Surgery

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06631118
Enrollment
60
Registered
2024-10-08
Start date
2024-10-21
Completion date
2025-02-15
Last updated
2024-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Difference in Reduction in Visual Analogue Score at 30 Minutes

Brief summary

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.

Interventions

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

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

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The difference in VAS scale30 min after giving propofol and the PENG block.The primary outcome will be difference in median reduction in VAS-D .

Contacts

Primary ContactMarwa Mamdouh Mohamed
marwaemam600@gmail.com01000205686
Backup ContactMohamed Mourad Ali
mohamed_mourad@med.asu.edu.eg01006512101

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026