Study which is related to pain relief after breast surgery

A Randomized Controlled Study to Evaluate the efficacy of Ultrasound guided Erector spinae block for postoperative analgesia after Mastectomy

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/11/047382

Enrollment

Registered

2022-11-17

Start date

Unknown

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

Health Condition 1: - Health Condition 2: C509- Malignant neoplasm of breast of unspecified site Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Erector Spinae block: Erector Spinae block Under ultrasound guided interfascial plane block Control Intervention1: control group: VAS Score for 24 hrs postoperatively

Eligibility

Inclusion criteria

Inclusion criteria: ASA PS Class I, II & III Elective unilateral modified radical mastectomy under GA

Exclusion criteria

Exclusion criteria: Not willing to participate BMI > 35kg/m2 Known allergy to local anesthetic Coagulopathies Renal/hepatic dysfunction

Design outcomes

Primary

Measure	Time frame
USG guided ESP block when combined with GA reduces perioperative analgesic requirementTimepoint: VAS SCORE - 1hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr, 8th hr, 9th hr, 10th hour, 11th hour, 12th hour, 14th hour, 16th hour, 18th hour, 20th hour, 22nd hour, 24th hour	—

Secondary

Measure	Time frame
To compare PONV in both groupsTimepoint: PONV at 0 hr, 1st hr, 4th hr, 8th hr, 12th hr and 24th hr	—

Countries

India

Contacts

Public ContactSHEENA M B

Government Kanyakumari Medical College and Hospital

edwardjohnson2310@gmail.com09443392974

Outcome results

None listed

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