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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | pericapsular 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 |
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.