Skip to content

Assessment of pain relief between erector spinae block and local wound site infiltration in patients undergoing lumbar spinal surgeries

The comparison of the efficacy between bilateral ultrasound guided erector spinae block versus incision site infiltration for duration of analgesia in lumbar spinal surgery using levobupivacaine: A prospective, randomized comparative study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059119
Enrollment
50
Registered
2023-10-26
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Inj Levobupivacaine 0.25% in Erector spinae block and local wound site infiltration: Inj Levobupivacaine 0.25% 20 ml will be injected in two separate groups to compare their efficacy po

Sponsors

Rajarajeswari medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 and 2 patients. Patients aged 20-65 yrs undergoing single level lumbar discectomy surgeries.

Exclusion criteria

Exclusion criteria: Patient refusal Patients with known hypersensitivity to local anaesthetics Patient with bleeding disorder, uncontrolled Diabetes Mellitus, severe Renal & Liver Diseases Patient with Epilepsy Mentally unstable patients

Design outcomes

Primary

MeasureTime frame
To compare & assess the analgesic efficacy postoperatively between Erector spinae block & local wound site infiltration.Timepoint: To compare & assess the analgesic efficacy postoperatively between Erector spinae block & local wound site infiltration in FIRST 24 hrs.

Secondary

MeasureTime frame
To compare the need of rescue analgesia postoperatively between Erector spinae block & local wound site infiltration Comparison of hemodynamic parameters. complications if anyTimepoint: Post operative period for first 24 hrs

Countries

India

Contacts

Public ContactPrajyot Bhurli

Rajarajeswari medical college and hospital

drgskarthik@gmail.com9538220515

Outcome results

None listed

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