Comparative study for post operative analgesic efficacy in breast carcinoma surgery patients

USG guided Erector Spinae block versus local infiltration during breast surgery with General Anaesthesia- A comparative study of analgesic effect post operatively A double blinded Randomised control trial

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061422

Enrollment

Registered

2024-01-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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 Plane Block (Group A) One-time bolus: Patient in this group will recieve USG guided erector Spinae plane block (one time bolus) at the end of surgery just before extubati

Eligibility

Inclusion criteria

Inclusion criteria: 1). American society of anaesthesiologists- Physical standards classification (ASA-PS) class II And class III individuals.

Exclusion criteria

Exclusion criteria: 1).Patient refusal 2).Age below 18 years and above 65 years 3).ASA-PS Class IV and above 4).Patient with known allergies to any drugs used 5).Local Infection at the site of block 6).Patients receiving opioids for chronic analgesic therapy 7).Inability to comprehend Visual Analogue scale

Design outcomes

Primary

Measure	Time frame
Duration of Analgesia and request for rescue analgesiaTimepoint: 24 hours	—

Secondary

Measure	Time frame
Visual Analogue score of pain and incidence of post operative nausea and vomitingTimepoint: Time frame of 2 hours 4 hours 6 hours 12 hours ad 24 hours	—

Countries

India

Contacts

Public ContactJohn Magesh

Armed Forces Medical College Pune

majjohnmk9090@gmail.com9765167438

Outcome results

None listed

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