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Compare between Ultrasound guided Pericapsular nerve group block and Suprainguinal fascia iliaca block for reducing pain during sitting position for spinal anaesthesia in patients of acetabular fractures undergoing open reduction and internal fixation

A randomized comparative study to evaluate the efficacy of ultrasound guided pericapsular nerve group block versus ultrasound guided suprainguinal fascia Iliaca block for ease of positioning during spinal anaesthesia in cases of acetabular fractures posted for open reduction and internal fixation SMS Medical College Jaipur - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102053
Enrollment
80
Registered
2026-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: 20ml of 0.25% Bupivaicaine and 2mg of Dexamethasone ( USG guided Suprainguinal fascia iliaca block ): The patient will be placed in the supine position. Following sterile preparation, d

Sponsors

Sawai Man Singh Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing open reduction and internal fixation for acetabular fracture under spinal anaesthesia 2.Patients consenting to participate. 3.Adult patients aged 18-65 Years. 4.Patients belonging to American Society of Anesthesiologists(ASA) grade I, II and III

Exclusion criteria

Exclusion criteria: 1.Patients who will not be able to assist in block assessment. 2.Those with preexisting neuropathy. 3.Having coagulopathy . 4.Allergic to local anesthetics. 5.Infection at the local site of administration of block 6.Patient should not be part of any other study.

Design outcomes

Primary

MeasureTime frame
1. To assess and compare NRS score at rest and on passive 15-degree limb elevation every 5min after the block till NRS less then 2 is achieved. 2. To assess and compare time taken to achieve NRS less then 2 in both the groups. 3. To assess and compare the difference in sitting angle before the block and at positioning for spinal anaesthesia between the two groups.Timepoint: 1. At baseline, 5 min, 10 min,15 min till NRS less then 2 2. At baseline, 5 min, 10 min, 15 min till NRS less then 2 3. At baseline, 15 min during positioning

Secondary

MeasureTime frame
1. To assess & compare NRS postoperatively every 6 hrly for 24hr between the groups 2. To determine & compare amount of Tramadol iv (mg) used in first 24 hr postoperatively in both the groups. 3. To observe any block related side effects such as nausea vomiting respiratory depression & LAST if any.Timepoint: 1. At baseline, 6 hr 12 hr 18 hr 24 hr 2. At baseline 6 hr 12 hr 18 hr 24 hr 3. At baseline 6 hr 12 hr 18 hr 24 hr

Countries

India

Contacts

Public ContactDr Aarushi Bhanu

Sawai Man Singh Medical College, Jaipur

vandanamangal25@gmail.com9829056816

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026