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Erector Spinae Plane (ESP) block in breast surgery

Ultrasound Guided Regional Blocks for Breast Surgery; A Comparison of Erector Spinae Plane (ESP), Thoracic Paravertebral (TPVB) and Serratus Anterior Plane (SAP) Blocks in Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/11/016389
Enrollment
60
Registered
2018-11-20
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- Female patients, aged between 18-70 years of age undergoing any breast surgery Health Condition 2: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: Ultrasound Guided Regional Blocks (Erector Spinae Plane Block, Thoracic Paravertebral Block and Serratus Anterior Plane Block) for Breast Surgeries: Each intervention will receive 20 ml

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patients undergoing elective unilateral breast surgeries with or without axillary clearance. Aged between 18-65 year of age ASA (American Society of Anesthesiology) Physical status I and II patients

Exclusion criteria

Exclusion criteria: Patients refusal to participate in the study History of coagulation disorders, antiplatelet therapy, anticoagulant therapy. Morbid obesity with BMI >=35kg/m2 Thoracic vertebral anomalies and severe chest wall deformity Known allergy to study drugs Patients with infection at the site of proposed block Pregnancy Severe cardiac, renal and hepatic conditions Thyrotoxicosis Mental retardation

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia produced by three regional anaesthetic techniques (ESP, TPVB and SAP blocks) in patients undergoing any breast surgery under general anaesthesia. Timepoint: immediate post operative period (0 hour) Then at 1st, 2nd, 4th, 6th, 12th, 18th and 24th hour of surgery—

Secondary

MeasureTime frame
Secondary Objectives 1. To compare the total rescue opioid or opioid equivalent drugs required in the first 24 hours after surgery. 2. To compare the complications associated with the three regional anaesthetic techniques. Timepoint: At 0, 1, 2, 3,6, 12 and 24 hours—

Countries

India

Contacts

Public ContactDr Praveen Talawar

AIIMS New Delhi

praveenrt64@gmail.com9654162941

Outcome results

None listed

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