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Effectiveness of Erector spinae plane block using Ultrasound machine for providing post-operative pain relief in Hip joint and proximal femur surgeries.

Efficacy of ultrasound guided erector spinae plane block for post-operative pain relief in hip joint and proximal femur surgeries- A randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032741
Enrollment
86
Registered
2021-04-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur Health Condition 2: M169- Osteoarthritis of hip, unspecified Health Condition 3: 8- Other Procedures Health Condition 4: M167- Other unilateral secondary osteoarthritis of hip Health Condition 5: S721- Pertrochanteric fracture Health Condition 6: S722- Subtrochanteric fracture of femur Health Condition 7: M163- Unilateral osteoarthritis resulting from hip dysplasia Health Condition 8: M165- Unilateral post-traumatic osteoarthrit

Interventions

Intervention1: Erector spinae plane block: Ultrasound guided lumbar erector spinae plane block for post-operative pain relief in hip joint and proximal femur surgeries Control Intervention1: Injection

Sponsors

Hetal Kotecha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grading- I,II,III Patient posted for hip joint and proximal femur surgeries Patient able to give verbal and informed consent Patient able to understand VAS regarding assessment of Pain

Exclusion criteria

Exclusion criteria: Patient not willing Allergy to local anesthetics Contraindication of spinal, regional anaesthesia Patient with coagulopathy, local infection Patient with pre-existing neurological deficits Patient with history of drug or alcohol abuse, psychiatric illness Patient with pelvic fracture

Design outcomes

Primary

MeasureTime frame
Duration of Analgesia and No of Rescue analgesic requirement within 24 hoursTimepoint: Pain will be assessed using VAS (Visual Analogue Scale) score every 1 hour for first 6 hours and every 6 hours for next 24 hours Rescue analgesia will be given in the form of Injection Paracetamol 15 mg/kg iv at VAS score more than 4—

Secondary

MeasureTime frame
Vital parameters and Complications associated with blockTimepoint: Vital parameters will be monitored before giving the block, immediately after giving the block, at 2, 5, 10, 30, 60 minutes—

Countries

India

Contacts

Public ContactDr Kavita Lalchandani

Government Medical College and SSG Hospital, Vadodara

lalchandanikavita@yahoo.co.in9274586809

Outcome results

None listed

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