It ia a study to compare ultrasound (US) guided Retrolaminar block and erector spinae block for post operative pain management in patients posted for elective breast surgery.

Assessment of ultrasound (US) guided Retrolaminar block and erector spinae block for post operative analgesia in patients undergoing modified radical mastectomy

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/07/044361

Enrollment

Registered

2022-07-26

Start date

Unknown

Completion date

Unknown

Last updated

2023-01-09

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 Health Condition 2: C501- Malignant neoplasm of central portion of breast

Interventions

Intervention1: Retrolaminar block to be used to provide analgesia in breast surgery: Retrolaminar block to be used before induction of general anaesthesia to provide analgesia in patients undergoing m

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1-3

Exclusion criteria

Exclusion criteria: do not give consent allergic to local anesthetics bleeding disorders BMI >25 pregnant alcohol or drug abuse advanced CVDs psychiatric illness

Design outcomes

Primary

Measure	Time frame
analgesia with retro laminar block and erector spine blockTimepoint: for 24 hours post operative analgesia with retro laminar block and erector spine block	—

Secondary

Measure	Time frame
Quality of anaesthesia Safety of retro laminar block, erector spine blockTimepoint: 24 hours post operative	—

Countries

India

Contacts

Public ContactPrashant Kumar

Pt. B.D. Sharma PGIMS Rohtak

pk.pgims@yahoo.com

Outcome results

None listed

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