Comparision of combining Pericapsular Nerve Group(PENG) block with Suprainguinal Fascia Iliaca Block (SIFICB) vs PENG Block for postoperative pain relief in Total Hip Replacement

Efficacy of Pericapsular Nerve Group(PENG) Block in combination with Suprainguinal Fascia Iliaca Block(SIFICB) for postoperative Analgesia after Total Hip Arthroplasty: A Randomised Controlled Trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/04/051593

Enrollment

Registered

2023-04-13

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-01

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

Conditions

Health Condition 1: M870- Idiopathic aseptic necrosis of bone Health Condition 2: M873- Other secondary osteonecrosis Health Condition 3: S721- Pertrochanteric fracture

Interventions

Intervention1: PENG Block With SIFIC Block: Total 30ml drug with 15ml of 0.5% Injection Bupivacaine with 2ml of Injection Dexamethasone (8gm) and Injection 13ml sterile water will be made. Out of whic

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients undergoing primary unilateral total hip arthroplasty under spinal anaesthesia 2) Patients conformed to American Society of Anaesthesiologists(ASA) physical status I-III in preoperative assessment 3) Ability to follow the study protocol

Exclusion criteria

Exclusion criteria: 1) Inability or refusal to follow study protocol 2) Coagulopathy 3) Sickle Cell Disease 4) Pre-existing lower extremity neuromuscular disorders 5) Local infection over the injection site 6) Allergy or contraindications to the drugs used in the study(local anaesthetics, NSAIDs, steroids) 7) Chronic opioid use

Design outcomes

Primary

Measure	Time frame
Changes in the postoperative pain intensity and pain control and total analgesic consumption post operatively after giving the blockTimepoint: Visual Analogue Scale(VAS) Score will be assessed at 6hrs,12hrs,24hrs and 48hrs after giving the block postoperatively	—

Secondary

Measure	Time frame
Ability to do quadriceps exercisesTimepoint: at 24hrs and 48hrs;Extent of motor blockade using bromage scaleTimepoint: at 6hrs, 12hrs, 24hrs;Postoperative ability of early ambulationTimepoint: at 24hrs and 48hrs;Rate of patient satisfactionTimepoint: from range of 1 to 5, 1 being very much satisfied and 5 being dissatisfied;Rate of postoperative complicationTimepoint: like local aneasthetic toxicity, falls nausea, vomiting	—

Measure

Time frame

Ability to do quadriceps exercisesTimepoint: at 24hrs and 48hrs;Extent of motor blockade using bromage scaleTimepoint: at 6hrs, 12hrs, 24hrs;Postoperative ability of early ambulationTimepoint: at 24hrs and 48hrs;Rate of patient satisfactionTimepoint: from range of 1 to 5, 1 being very much satisfied and 5 being dissatisfied;Rate of postoperative complicationTimepoint: like local aneasthetic toxicity, falls nausea, vomiting

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Countries

India

Contacts

Public ContactDr Devyani Desai

Baroda Medical College and SSG Hospital, Vadodara

devyani.dr@gmail.com9909983168

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026