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Comparison of the pain relieving effect of two approaches to the ultra-sound guided back muscle in patients undergoing breast operation

Comparison of the analgesic efficacy two approaches to the ultra-sound guided erector spinae plane block in patients undergoing modified radical mastectomy: A randomized controlled trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059468
Enrollment
60
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Interventions

Control Intervention1: Group A (BTWN): Patients will receive erector spinae plane block with 20 ml 0.375% ropivacaine injection administered between transverse processes prior to general anaesthesia.

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) ASA I- II b) Scheduled to undergo elective modified radical mastectomy

Exclusion criteria

Exclusion criteria: a) Patient refusal for regional techniques b) All contra-indications to regional techniques: Local or systemic infection Known allergy to the study drugs Bleeding disorders Platelet count c) BMI > 35 d) Inability to use PCA device post operatively

Design outcomes

Primary

MeasureTime frame
Efficacy of analgesic technique determined by 11-point numeric rating scale (NRS) at rest & on abduction of ipsilateral arm above the head.Timepoint: Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours—

Secondary

MeasureTime frame
24-hour fentanyl consumptionTimepoint: 1st 24 hours of post-operative period;Intraoperative opioid consumption.Timepoint: Intraoperative period; ? Incidence of adverse events (postoperative nausea/ vomiting, respiratory depression, pruritus, urinary retention) retention)Timepoint: 1st 24 hours of post-operative period.;Patient satisfaction scoreTimepoint: Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours;Time to first analgesic requirement in post-operative period.Timepoint: 1st 24 hours of Post operative period—

Countries

India

Contacts

Public ContactKunal Aggarwal

All India Institute of Medical Sciences

dr.mritunjay@gmail.com09868023165

Outcome results

None listed

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