CTRI/2020/07/026448Not yet recruitingPhase 3 4
Comparative efficacy of peri-operative analgesia and ease of spinal position between ultrasound guided Pericapsular Nerve Group (PENG) block and Supra Inguinal Fascia Iliaca (SIFI) block in hip surgeries – A double blinded randomized controlled trial.
S Nijalingappa Medical College and HSK Hospital1 site in 1 country90 target enrollmentStarted: October 7, 2020Last updated:
Trial Snapshot
- Phase
- Phase 3 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 90
- Locations
- 1
- Primary Endpoint
- Assessment of perioperative analgesia by numerical rating scale (NRS) between two study groups at rest and straight leg raise of affected limb to 15 degrees
Study Overview
Brief Summary
The objective of this randomized control study is comparison of analgesic efficacy and ease of spinal position between ultrasound guided pericapsular nerve group block versus suprainguinal fascia iliac block for patients posted to hip surgeries.
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Participant and Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •ASA I–Ⅲ patients Body mass index ≤30 kg/m2 Patients undergoing elective hip surgeries like femur neck intertrochanteric and subtrochanteric fracture.
Exclusion Criteria
- •Patient refusal to give consent.
- •Infection at site of injection.
- •Allergy to local anaesthetics.
- •Patients receiving opioids for chronic analgesic therapy.
- •Coagulopathy Patients with inguinal hernia on the same side of hip pathology.
Outcomes
Primary Outcomes
Assessment of perioperative analgesia by numerical rating scale (NRS) between two study groups at rest and straight leg raise of affected limb to 15 degrees
Time Frame: NRS pain score 30 minutes before and after administration of block
Secondary Outcomes
- Ease of spinal position between two groups by using ease of spinal position scale (EOSP).(Comparison of amount of consumption of rescue analgesia between two groups.)
Investigators
Study Sites (1)
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