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Evaluation of lumbar erector spinae plane block for postoperative pain relief for lumbar spine surgeries

LUMBAR ERECTOR SPINAE PLANE BLOCK FOR POST OPERATIVE ANALGESIA FOR LUMBER SPINE SURGERY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/053002
Enrollment
60
Registered
2023-05-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: M489- Spondylopathy, unspecified

Interventions

Intervention1: lumbar erector spinae: 20 mls of 0.375% ropivacaine is deposited each side between transverse process and erector spinae in lumbar region. Control Intervention1: conventional group: onl

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing lumber spinae surgery under general anaesthesia Age group: 20 - 80 years BMl-18.5-29.9 American society of anaesthesiology (ASA) grade 1 and 2 patients of either sex

Exclusion criteria

Exclusion criteria: Patient refusal Patients undergoing cervical, thoracic spine surgeries ASA 3 and above Patients with local infection at the site of block Patients with history of bleeding disorder or on anti coagulant therapy Patients with known allergy to local anaesthetic drugs Patients with mental illness or dementia

Design outcomes

Primary

MeasureTime frame
Pain Score using VAS Timepoint: 2, 4 ,6 , 12 , 18, 24 hrs—

Secondary

MeasureTime frame
SEDATION SCORETimepoint: 2, 4 ,6 , 12 , 18, 24 hrs;PATIENT SATISFACTION SCORETimepoint: 24 hr;PONVTimepoint: 2, 4 ,6 , 12 , 18, 24 hrs;Total Rescue Analgesic requirementTimepoint: 24 hr—

Countries

India

Contacts

Public ContactDr Anjali

ASIAN HOSPITAL FARIDABAD

drdivesh@gmail.com9650099113

Outcome results

None listed

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