USG guided Ilioinguinal and Iliohypogastric nerve block for post operative analgesia in unilateral inguinal hernia surgeries under spinal anaesthesia. A Randomised control trial study
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Post operative pain score assessed using visual analogue scale
Study Overview
Brief Summary
This prospective, randomized interventional study aims to evaluate the efficacy of ultrasound-guided ilioinguinal and iliohypogastric nerve block in providing postoperative analgesia in patients undergoing unilateral inguinal hernia repair under spinal anaesthesia. Pain intensity will be assessed using the Visual Analogue Scale (VAS) at multiple postoperative intervals, and outcomes will include total analgesic consumption, time to first rescue analgesia, and any block-related complications over 24 hours. The study seeks to determine whether the nerve block improves pain control and reduces analgesic requirements compared to standard care.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Participant Blinded
Eligibility Criteria
- Ages
- 20.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients between age of 20 to 60 years of ASA physical status 1 and 2 undergoing elective non relapsing unilateral inguinal hernia repair.
Exclusion Criteria
- •Patients with known allergy to local anaesthetics patient with chronic pain not related to inguinal hernia patient with contraindication to spinal anaesthesia and patients with obstructed or strangulated hernia.
Outcomes
Primary Outcomes
Post operative pain score assessed using visual analogue scale
Time Frame: Post operative pain score assessed using visual analogue scale VAS at 1 2 3 4 6 12 24 hours after surgery
Secondary Outcomes
- Total rescue analgesia requirement(Total analgesic requirements in 24 hour since block)
Investigators
Moon Prajwal Annaji
vIlasrao deshmukh government medical college Latur