Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06631118

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
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
40 Years – 70 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

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

Timeline

Start date
2024-10-21
Primary completion
2025-01-31
Completion
2025-02-15
First posted
2024-10-08
Last updated
2024-10-08

Source: ClinicalTrials.gov record NCT06631118. Inclusion in this directory is not an endorsement.