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Comparison of efficacy in pain relief ,changes in pulse rate, blood pressure and surgeon s satisfaction between landmark guided, C-Arm guided And USG guided erector spinae block in lumbar spine surgery

Evaluation Of landmark guided, C-Arm guided And USG guided erector spinae block in terms of perioperative analgesia, hemodynamics snd surgeon s satisfaction following lumbar spine fixation surgery

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083314
Enrollment
120
Registered
2025-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: EVALUATION OF LANDMARK GUIDED, C-ARM GUIDED AND USG GUIDED ERECTOR SPINAE BLOCK IN TERMS OF PERIOPERATIVE ANALGESIA,HEMODYNAMICS AND SURGEON’S SATISFACTION FOLLOWING LUMBER SPINE FIXATI

Sponsors

R. G. KAR MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Posted for lumbar spine fixation surgeries 2. 2 or 3 level lower lumbar spine (L3-L4/L4-L5) surgery by posterior approach 3. ASA Grade 1 and 2 patients 4. Age between 18-60 years of either sex 5. Patients with BMI between20-30

Exclusion criteria

Exclusion criteria: 1. Uncooperative patients or refusal. 2. ASA Grade 3 or above 3. Duration of surgery more than 2 hours 4. Cardiac and neurological diseases. 5. Uncontrolled Diabetes and Hypertension. 6. Chronic Obstructive Pulmonary Disease and Bronchial Asthma. 7. Bleeding disorder 8. On psychiatric medication. 9. Known allergy to the drug used. 10. Epilepsy. 11. Any kind of preexisting neuropathy. 12. Alcoholism. 13. Chronic opioid use (Defined as daily and almost daily use of opioids for more than 3 months).

Design outcomes

Primary

MeasureTime frame
To compare the duration of post-operative analgesia.(timing of first rescue analgesic) 2) Grade of sensory block through touch and pin prick method. 3) Motor function of leg will be evaluated with a Bromage (0-3) score. Timepoint: JUNE 2023 TO JUNE 2024

Secondary

MeasureTime frame
i) Intraoperative haemodynamics with respect to changes in HR and MAP. ii) Intraoperative bleeding using Boezzart’s scale iii) Intraoperative surgeons’ satisfaction using Likert scale iv) Postoperative analgesic consumption in first 24 hr v) Frequency of postoperative analgesic administration. Timepoint: JUNE 2023 TO JUNE 2024

Countries

India

Contacts

Public ContactSONALINA MUDI

R. G. KAR MEDICAL COLLEGE AND HOSPITAL

sonalina.mudi701@gmail.com9051283086

Outcome results

None listed

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