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Ultrasound guided bilateral block of erector spinae muscle, a muscle in back to reduce pain after traumatic spine surgery

Bilateral ultrasound guided erector spinae plane block for postoperative pain relief in traumatic spinesSurgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018206
Enrollment
34
Registered
2019-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: M898- Other specified disorders of bone

Interventions

Intervention1: Bilateral Ultrasound guided erector spinae plane block for postoperative pain relief in traumatic spine surgery : A randomised controlled trial: Technique of ESP block: High frequency l

Sponsors

Dr Babita Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All adults with traumatic spine injury (thoracic/ lumbar spine ) with ASIA grade B to E (i.e with intact sensory function) posted for traumatic spine fixation surgery during the study period. 2. American society of Anaesthesiologist (ASA) grade I/II patients 3. body mass index 20 to 35 kg/m2

Exclusion criteria

Exclusion criteria: 1.Patients refusal 2.Known allergy to local anaesthetic drugs 3.Abnormal back or spine anatomy 4.Infection at the injection site 5.Pregnancy 6.Incision involving more than 6 intervertebral spaces 7.Altered coagulation profiles( PTINR >1.5, platelet count <100,000/cmm)

Design outcomes

Primary

MeasureTime frame
24 hours opioid consumption (time frame: 24 hours from injection)Timepoint: 24 hours opioid consumption (time frame: 24 hours from injection)—

Secondary

MeasureTime frame
1. Pain score ( time frame : 24 hour postoperative at regulsr intervals 0,3,6,12,18 and 24 hours) visual analog scores postoperative pain (0-10) 2. Time of first analgesic dose 3.Postoperative nausea and vomiting 4.Extent of sensory blockade anterior and posteriorly in the immediate postoperative period.Timepoint: 24 hours—

Countries

India

Contacts

Public ContactBaby Pegu

All India Institute of Medical Science

drbabitagupta@hotmail.com9868397815

Outcome results

None listed

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