FindTrial
Sign In

Comparison of severity of pain of multiple local anaesthetic nerve blocks and intravenous painkillers for breast surgery

Comparison of analgesic efficacy (intra and post operatively) of ultrasound guided Erector spinae plane block, Serratus anterior plane block, Paravertebral plane block and intravenous opioids for modified radical mastectomy- A prospective randomised controlled trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064565
Enrollment
44
Registered
2024-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: C501- Malignant neoplasm of central portion of breast Health Condition 2: C503- Malignant neoplasm of lower-innerquadrant of breast Health Condition 3: C505- Malignant neoplasm of lower-outerquadrant of breast Health Condition 4: C502- Malignant neoplasm of upper-innerquadrant of breast Health Condition 5: C504- Malignant neoplasm of upper-outerquadrant of breast

Interventions

Intervention1: Serratus anterior plane block: Under ultrasound guidance,with patient in supine position and arm abducted to 90 degrees,0.3 ml/kg of 0.25% BUPIVACAINE is injected in plane between muscl

Sponsors

NARAYANA HRUDHAYALAYA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.More than 18 years with breast cancer 2.American society of anesthesiologists physical status I to III. 3.patients who have given informed written consent.

Exclusion criteria

Exclusion criteria: Body mass index more than 40 Local anaesthetic allergy Local infection at the site of block Respiratory or neurological disease.

Design outcomes

Primary

MeasureTime frame
To document and compare cumulative opioid consumption intraoperatively and 24 hours postoperatively in all 4 groupsTimepoint: To document and compare cumulative opioid consumption intraoperatively and 24 hours postoperatively in all 4 groups—

Secondary

MeasureTime frame
1.Time of first rescue analgesic 2.Interval between opioid doses. 3.NRS score at rest,6,12,18,24 hours. 4.Complications of each technique 5.Postoperative nausea and vomiting 6.HemodynamicsTimepoint: During surgery and 24 hours post surgery.—

Countries

India

Contacts

Public ContactDrDIVYA DHARSHINIVP

NARAYANA HRUDHAYALAYA LTD.

drmaama@yahoo.com9449000426

Outcome results

None listed

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