comparison of erector spinae block for post operative pain relief in lumbar spine surgery

comparison of erector spinae block for postoperative analgesia in lumbar spine surgery-A randomized control trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/02/012143

Enrollment

Registered

2018-02-26

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- patients posted for spine surgery of lumbar region

Interventions

Intervention1: Erector spinae block with 0.25% Bupivacaine: Erector spinae block would be given and 0.25% bupivacaine 20ml would be injected Control Intervention1: Erector spinae block with 20 ml 0.25

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1,2,3 Age group 18- 65 years

Exclusion criteria

Exclusion criteria: ASA grade 4 Any allergy to local anaesthetics Patients refusal Infection at site of intervention

Design outcomes

Primary

Measure	Time frame
total volume of postoperative analgesia requiredTimepoint: 24 hr	—

Secondary

Measure	Time frame
patients satisfaction scoreTimepoint: 24 hr	—

Countries

India

Contacts

Public ContactDr neeraj kumar chaudhary

IGIMS,PATNA

neerajpankaj043@yahoo.com9304383720

Outcome results

None listed

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