Ultrasound guided Erector spinae plane block versus Retrolaminar block for post operative analgesia for patients undergoing Modified Radical Mastectomy

Ultrasound guided erector spinae plane block versus retrolaminar block for post operative analgesia in patients under going modified radical mastectomy- a randomised controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/11/097090

Enrollment

Registered

2025-11-07

Start date

Unknown

Completion date

Unknown

Last updated

2025-11-17

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

Conditions

Health Condition 1: C504- Malignant neoplasm of upper-outerquadrant of breast

Interventions

Intervention1: Erector Spinae Plane block: Nerve block needle will be inserted under USG guidance to contact tip of the T4 transverse process for Erector Spinae Plane block and a total of 25 ml 0.25 %

Eligibility

Inclusion criteria

Inclusion criteria: Posted for unilateral Modified Radical Mastectomy under General anesthesia

Exclusion criteria

Exclusion criteria: ASA Class IV History of daily consumption of opiods and analgesics Previous surgery in thoracic vertrbral region BMI more than 30 Any infection at block site Previous allergy to drug used for the study

Design outcomes

Primary

Measure	Time frame
To compare post operative analgesic efficacy of Erector Spinae Plane block and Retrolaminar Block in terms of the time taken to receive first rescue analgesic in patients undergoing Unilateral Modified Radical MastectomyTimepoint: 24 hours	—

Secondary

Measure	Time frame
To assess the intensity of pain during the first 24 hours using VAS score To assess the total rescue analgesics consumption over 24 hours To assess the occurrence of complications like Post operative nausea and vomiting (PONV), Hematoma Timepoint: 24 HOURS	—

Countries

India

Contacts

Public ContactDr Pradeesh Johny

bommidisrk@gmail.com9894723687

Outcome results

None listed

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