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Comparison of ultrasound guided thoracic block by two different approach in breast surgeries

"Comparison of ultrasound guided thoracic paravertebral block versus ultrasound guided thoracic erector spinae plane block for postoperative analgesia in Modified Radical Mastectomy: A Prospective Randomized Study"

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023252
Enrollment
60
Registered
2020-02-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: thoracic paravertebral block: Paravertebral Block (TPVB) by usingan ultrasound to guide the needle tip to a point between the costotransverse ligament and the parietal pleura between th

Sponsors

Jyoti mala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for unilateral MRM operation Patients able to comprehend, willing to participate &Willing to give written informed consent in English or Hindi Patients of ASA physical status 1, 2& 3 Patients between 20 - 60 years of age of either sex

Exclusion criteria

Exclusion criteria: Patientâ??s refusal to participate Patients of ASA physical status 4 Any allergy to local anaesthetics Coagulation disorders Infection at the site of intervention History of any underlying cardiac, renal or hepatic dysfunction Pregnant patient Age less than 20 or greater than 60 years Chronic opioid use or drug abuse Significant psychiatric disturbance Refusal to provide written consent

Design outcomes

Primary

MeasureTime frame
1.Pain score at the interval of 2, 4, 6 12, & 24 hour Pain score via Numeric Rating Scale (0-10) 2.Total opioid consumption for 24 h in postoperative period Timepoint: 6 months

Secondary

MeasureTime frame
1.Hemodynamic changes 2.Patient satisfaction score 3.any adverse effect in either group Timepoint: 6 months

Countries

India

Contacts

Public ContactSwati

IGIMS

deepakswat@yahoo.com854441341

Outcome results

None listed

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