To compare of ultrasound guided erector spinae block versus paravertebral block for post operative pain management in breast surgeries

Comparison of ultrasound guided erector spinae block versus paravertebral block for post operative analgesia in breast surgeries - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084574

Enrollment

Registered

2025-04-11

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: Erector spinae block (Group E): Group E : 0.25% levobupivacaine 30ml Control Intervention1: Paravertebral block (Group P): O.25% levobupivacaine 30ml

Eligibility

Inclusion criteria

Inclusion criteria: ASA Class 1 or 2 BMI 18 to 35 kg/m2

Exclusion criteria

Exclusion criteria: Patient refusal Know Hypersensitivity to LA Chronic systemic illness Bleeding diathesis Infection at local site Pregnancy Patient with spinal deformities

Design outcomes

Primary

Measure	Time frame
To compare the time to first rescue analgesia in both study groups.Timepoint: 30mins,60mins,120mins4hrs,8hrs,12hrs,24hrs,48hrs.	—

Secondary

Measure	Time frame
To compare the total tramadol consumption for 1st 24hrs. VAS score at 1hr,4hrs,12hrs,24hrs. Complications following erector spinae block and paravertebral blockTimepoint: 30mins,60mins,120mins,4hrs,8hrs,12hrs,24hrs,48hrs.	—

Countries

India

Contacts

Public ContactRKrishnaprabu

Sri Venkateswara medical college hospital and research centre

drkrishnaprabu@gmail.com9943770977

Outcome results

None listed

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