Comparison of pain relieving effect of ultrasound guided lateral (modified) erector spinae plane block with erector spinae plane block in patient undergoingModified breast surgery

Comparison of analgesic efficacy of ultrasound-guided lateral erector spinae plane block versus erector spinae plane block in patient undergoing Modified Radical Mastectomy: A randomised control trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075355

Enrollment

Registered

2024-10-16

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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: USG guided lateral erector spinae plane block: After GA, a 21-gauge, 8 cm insulated echogenic needle will be inserted under real-time in-plane between the erector spinae and 5th rib jus

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I and II 2. Patients between the ages of 18-70 years 3. Duration of surgery less than 3 hrs 4. Female 5. BMI 18-30kg/m2

Exclusion criteria

Exclusion criteria: History of severe liver, renal or cardiovascular disease or chronic pain disease 2. Pre-existing neurological or psychiatric illness 3. Any bleeding abnormality 4. Diagnosis of allergy to the study drug 5. History of alcohol or drug abuse 6. History of chronic use of analgesics, sedatives, opioids, or steroids 7. Pregnancy 8. Uncooperative (due to dementia, mental retardation, etc.) 9. Procedure site infection 10. History of previous mastectomy 11. Severe spine/chest wall deformity

Design outcomes

Primary

Measure	Time frame
To compare postoperative opioid consumptionTimepoint: 24 h postoperatively	—

Secondary

Measure	Time frame
1. Time to first rescue analgesia 2. Total intraoperative opioid consumption 3. Numerical rating score of pain in first 24 hours post operatively 4. PONVTimepoint: 1. After surgery 2. Till the end of surgery 3. At 1st, 2nd, 6th, 12th, 24th hour 4. Till 24 hour postoperatively	—

Countries

India

Contacts

Public ContactDr Shagufta Naaz

All India Institute of Medical Sciences, Patna

drshaguftanaaz@gmail.com7765937919

Outcome results

None listed

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