Study to compare the effectiveness of drug given under direct vision and under ultrasound to blunt the pain after breast removal surgery

A comparative study to evaluate analgesic efficacy of pre operative and intraoperative pectoralis nerve block for patients undergoing Modified Radical Mastectomy - PEC

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/063317

Enrollment

Registered

2024-02-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: A COMPARATIVE STUDY TO EVALUATE ANALGESIC EFFICACY OF PRE OPERATIVE AND INTRA OPERATIVE PEC BLOCK FOR PATIENTS UNDERGOING MODIFIED RADICAL MASTECTOMY : To evaluate the effect of pre ope

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing unilateral modified radical mastectomy under general anesthesia. Age group between 18 to 65 years of either gender, giving valid informed and written consent. American Society of Anaesthesiologist grade I and II

Exclusion criteria

Exclusion criteria: Patients with any contraindication to regional anesthesia. Patients with a history of anaphylaxis to local anaesthetics and allergy to the study drugs. Pregnant or lactating patients.

Design outcomes

Primary

Measure	Time frame
To evaluate the effect of pre operative USG guided and intra operative pectoral nerve block with 30ml 0.25% ropivacaine each for pain relief for patients undergoing MRM.e pre operative USG guided and intraoperative under vision pectoral nerve block. Analgesic efficacy evaluated with VAS score and the duration until first rescue analgesic given.Timepoint: Outcome will be assessed at the end of study of 1.5 yrs.	—

Measure

Time frame

To evaluate the effect of pre operative USG guided and intra operative pectoral nerve block with 30ml 0.25% ropivacaine each for pain relief for patients undergoing MRM.e pre operative USG guided and intraoperative under vision pectoral nerve block. Analgesic efficacy evaluated with VAS score and the duration until first rescue analgesic given.Timepoint: Outcome will be assessed at the end of study of 1.5 yrs.

—

Secondary

Measure	Time frame
The need for rescue analgesic after the USG guided & undervision pec blockTimepoint: Outcome will be assessed with in 24 hours of pec block	—

Countries

India

Contacts

Public ContactHaramritpal Kaur

Guru Gobind Singh Medical College Faridkot

amritk_dr@yahoo.co.in9878088013

Outcome results

None listed

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