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Effect of thoracolumbar muscle plane block on postoperative pain and inflammation in spine surgery patients.

Comparison of the Post-operative pain and its association with Interleukins with or without Classical Thoracolumbar Inter-fascial Plane Block in Lumbar Spine Surgeries: A Prospective Double-blinded Randomized Controlled Trial. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072070
Enrollment
90
Registered
2024-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: G544- Lumbosacral root disorders, not elsewhere classified Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Single shot Classical thoracolumbar fascial plane block + standard pain management protocol: Classical thoracolumbar fascial plane block using 20 ml of 0.375% Ropivacaine, + Inj. Parace

Sponsors

Ruchi Verma Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who will give consent, ASA Physical status I or II, Scheduled for lumbar spine surgery

Exclusion criteria

Exclusion criteria: Patients with allergy to local anaesthetic, Coagulaton disorder, Infection at injection site, Chronic NSAID or opioid use, BMI more than 30 Kg/m2, Patients with neuromuscular disorder, Patients having chronic inflammatory disease, Patients with pre- existing autoimmune diseases

Design outcomes

Primary

MeasureTime frame
Post-operative pain assessment as per Visual analog scale (VAS) score.Timepoint: VAS score at 1, 6, 12, 24 and 48 hours in postoperative period in both the group.

Secondary

MeasureTime frame
1. Variation in Serum levels of IL-1, IL-6, IL-4 and IL-10 2. Total Intraoperative opioid consumption, 3. Postoperative rescue analgesia requirement 4. Postoperative nausea and vomiting 5. Time to hospital discharge. Timepoint: 1. At baseline, 6 hours, 24 hours and 48 hours 2. At the end of surgery 3 & 4. 1 hour, 6 hours, 12 hours, 24 hours and 48 hours

Countries

India

Contacts

Public ContactRuchi Verma

Sanjay Gandhi Post Graduate Institute of Medical Sciences

shreyachhabra0504@gmail.com7456022063

Outcome results

None listed

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