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COMPARATIVE STUDY FOR ALLEVIATING PAIN IN PATIENTS UNDERGOING HIP SURGERY- RANDOMISED CONTROL TRIAL.

A COMPARATIVE STUDY FOR ANALGESIC EFFICACY OF ULTRASOUND GUIDED ERECTOR SPINAE PLANE BLOCK VERSUS SUPRA INGUINAL FASCIA ILIACA BLOCK IN PATIENTS UNDERGOING HIP ARTHROPLASTY- A DOUBLE BLINDED RANDOMISED CONTROL TRIAL.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057500
Enrollment
60
Registered
2023-09-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: M258- Other specified joint disorders

Interventions

Intervention1: ESPB Group A This group will receive ultrasound-guided erector spinae plane block and subarachnoid block.(15 ml bupivacaine 0.5%, 15 ml normal saline): Patients will be placed in the l

Sponsors

AFMC PUNE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I to II. Patient scheduled for hip replacement surgeries under subarachnoid block(SAB). e.g. hip hemi-arthroplasty, total hip arthroplasty

Exclusion criteria

Exclusion criteria: 1)Patient refusal 2)age below 18 years or above 65 years 3)ASA grade III or IV 4)Patient with known allergies to any of the Drug Used 5)Contraindication to SAB e.g.Coagulopathy, infection at the injection site, severe cardio-pulmonary disease, diabetic or other neuropathies. 6)Patients recieving opioids for chronic Analgesic therapy. 7)Inability to comprehend Visual analogue scale(VAS) 8)Infection at site of erector spinae or fascia iliaca block 9)Body mass index >35kg/m2.

Design outcomes

Primary

MeasureTime frame
Total Opioid Requirements. Amount of opioids required postoperatively.Timepoint: Amount of opioids required in initial 24 hour period postoperatively.

Secondary

MeasureTime frame
1).Visual Analogue Pain Score( VAS At time frame of rest,2,4,6,12,18 and 24 hours postoperatively). 2). Time to first postoperative analgesic Request( Time Frame: 24 hours postoperatively). 3). Quadriceps Muscle power strength( Time Frame 6,12 and 24 hours postoperatively).Timepoint: 24 Hours postoperatively

Countries

India

Contacts

Public ContactJOHN M K

Dept of Anaesthesiology And Critical Care, AFMC, Pune 411040

docrahulyadav@gmail.com9350035558

Outcome results

None listed

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