PENG vs SIFI Block for Positioning Pain During Spinal Anesthesia
- Conditions
- Hip FracturesNerve BlockSpinal AnesthesiaAcute Post Operative Pain
- Interventions
- Other: PENG BlockOther: SIFI compartment blockDiagnostic Test: Numeric Rating ScaleDiagnostic Test: Angle of sitting
- Registration Number
- NCT05549011
- Lead Sponsor
- Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
- Brief Summary
This study aims to compare the effectiveness of preoperative ultrasound-guided suprainguinal fascia iliaca compartment block (SFICB) and pericapsular nerve group block (PENG) in preventing positioning pain during spinal anesthesia in patients who are scheduled for surgery due to hip fracture.
- Detailed Description
Patients to whom an analgesic block was placed (either PENG or SIFI compartment analgesic block) to ameliorate positioning pain during spinal anesthesia for hip fracture surgery will be enrolled after written consent is obtained. Patients will be asked to report their pain intensity while sitting and their sitting angle will be measured. Patients will be observed for any possible complications( LAST, allergic reactions, hypotension, bradycardia). Pain intensity will then again be questioned postoperatively along with analgesic consumption at the 24th hour. Patients will be arranged into two cohorts according to the block (PENG vs SIFI) and the data obtained will be compared between two cohorts.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 52
- Adults with a hip fracture
- who were scheduled to undergo surgery with spinal anesthetics
- has no neurologic disorders that impair cooperation (e.g dementia)
- has no true allergies to local anesthetics
- has no contraindications for regional or neuraxial anesthesia (e.g bleeding diathesis, severe aortic stenosis)
- Childer under the age of 18
- patients scheduled to undergo surgery with general anesthetics
- refusing to participate
- allergies to local anesthetics
- any neurologic disorder that impairs patient cooperation
- any contraindication to regional or neuraxial anesthetics
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description PENG block Angle of sitting This cohort will include participants to whom a PENG block is performed before positioning for spinal anesthesia PENG block PENG Block This cohort will include participants to whom a PENG block is performed before positioning for spinal anesthesia PENG block Numeric Rating Scale This cohort will include participants to whom a PENG block is performed before positioning for spinal anesthesia SIFI block SIFI compartment block This cohort will include participants to whom a SIFI compartment block is performed before positioning for spinal anesthesia SIFI block Numeric Rating Scale This cohort will include participants to whom a SIFI compartment block is performed before positioning for spinal anesthesia SIFI block Angle of sitting This cohort will include participants to whom a SIFI compartment block is performed before positioning for spinal anesthesia
- Primary Outcome Measures
Name Time Method Positioning pain during spinal anesthesia with 10-point numeric rating scale (NRS) 30 minutes after the block is placed NRS is a self-reported pain scale where patient defines intensity of their pain on a scale of 0 to 10. Zero means the patient has no pain while ten means the patient is experiencing the worst pain possible
- Secondary Outcome Measures
Name Time Method Postoperative pain with 10-point numeric rating scale (NRS) Postoperative day 1 NRS is a self-reported pain scale where patient defines intensity of their pain on a scale of 0 to 10. Zero means the patient has no pain while ten means the patient is experiencing the worst pain possible
Sitting angle during positioning 30 minutes after the block is placed Angle of sitting in degrees measured with a protractor during sitting for spinal anesthesia
Trial Locations
- Locations (1)
Prof. Dr. Cemil Taşcıoğlu City Hospital
🇹🇷Istanbul, Turkey