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A CLINICAL STUDY ON ULTRASOUND GUIDED CONTINUOUS SUPRAINGUINAL FASCIA BLOCK INFUSION AND CONTINUOUS FEMORAL NERVE BLOCK INFUSION FOR POST SURGERY PAIN IN PATIENTS UNDERGOING HIP REPLACEMENT DONE UNDER GENERAL ANAESTHESIA

A randomised controlled, Double blinded study on Ultrasound guided Continuous Suprainguinal Fascia Iliaca block infusion vs Continuous Femoral Nerve block infusion for postoperative analgesia in patients undergoing Total Hip Arthroplasty done under General Anaesthesia - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058647
Enrollment
80
Registered
2023-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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: NERVE BLOCK TECHNIQUES - SUPRAINGUINAL FASCIA BLOCK AND FEMORAL NERVE BLOCK: WE ARE COMPARING SUPRAINGUINAL FASCIA BLOCK AND FEMORAL NERVE BLOCK IN HIP ARTHROPLASTY PATIENTS FOR POSTOPE

Sponsors

SRM INSTITUTES FOR MEDICAL SCIENCE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 ASA GRADE 1 AND 2 2 ALL GENDERS 3 PATIENT ADMITTED FOR TOTAL HIP ARTHROPLASTY 4 PATIENT WILLING TO PARTICIPATE IN THIS STUDY 5 AGE 20-75 YEARS

Exclusion criteria

Exclusion criteria: 1 ASA GRADE 3 AND 4 2 AGE 75 YEARS 3 PREGNANT AND LACTATING MOTHERS 4 OBESE INDIVIDUALS WITH BMI MORE THAN OR EQUAL TO 30 5 PATIENTS PARTICIPATING IN ANY OTHER CLINICAL STUDIES 6 PATIENTS ALLERGIC TO LOCAL ANAESTHETICS AND ANY OTHER DRUGS USED IN THIS STUDY 7 PATIENT NOT WILLING TO PARTICIPATE IN THIS STUDY

Design outcomes

Primary

MeasureTime frame
TO STUDY THE POSTOPERATIVE ANALGESIA IN GROUP A AND GROUP BTimepoint: 48HOURS—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactMADHAVAN M

SRM INSTITUTES FOR MEDICAL SCIENCE

maddysuxa2@gmail.com9381513969

Outcome results

None listed

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