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Comparison between pain reducing effect of Thoracolumbar Interfascial plane block vs sacral erector Spinae plane block in participants undergoing lower spine surgeries.

Comparison between analgesic efficacy of Thoracolumbar Interfascial plane plane vs sacral erector Spinae plane block in patient undergoing lower spine lower spine surgeries. - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084843
Enrollment
138
Registered
2025-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M513- Other thoracic, thoracolumbar andlumbosacral intervertebral disc degeneration

Interventions

Intervention1: Sacral erector spinae plane block: The patient is made to lie in prone position. Under AAP, in prone position, linear probe/curvilinear 5-12Hz will be placed longitudinally in the

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I-II 2.Age 18-65yrs 3.Patient undergoing elective lower spine surgeries

Exclusion criteria

Exclusion criteria: 1.Patient refusal to participate. 2.known hypersensitivity to local anaesthetic and opioids 3.Patient having infection at the site of block 4.Patients on anticoagulant therapy 5.Patient with extensive lower spine surgeries like large tumor excision,

Design outcomes

Primary

MeasureTime frame
Total analgesic requirement (cumulative fentanyl consumption in 24hrs)Timepoint: Total analgesic requirement (cumulative fentanyl consumption in 24hrs)

Secondary

MeasureTime frame
To compare the following parameters in two study group: 1.Intra operative hemodynamics 2.Intra operative fentanyl consumption. 3. Time to first rescue analgesic required after surgery in post operative period. 4.NRS scores for pain & PONV in post operative period at 30m, 1h,2h,4h,6h,12h & 24h 5.adverse event during or after surgery related to intervention.Timepoint: 1. To assess the 24hrs postoperative pain using NRS scale 2. To assess the time for the first rescue analgesia injection requirement. 2. Patients satisfactory score will be asked.

Countries

India

Contacts

Public ContactPratiksha Darwade

AIIMS, New Delhi

ravindrapandey1972@gmail.com9773500767

Outcome results

None listed

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