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A study comparing two anesthetic blocks namely erector spinae block and modified pectoral nerve block for post surgical analgesia in patients undergoing breast cancer surgeries under general anesthesia.

Comparative evaluation of efficacy of Erector Spinae Plane Block and Modified Pectoral Nerve Block for Postoperative analgesia in patients undergoing breast malignancy surgeries under General anesthesia: A Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087897
Enrollment
60
Registered
2025-05-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: C500- Malignant neoplasm of nipple and areola

Interventions

Intervention1: Modified Pectoral Nerve Block: After giving general anaesthesia to patient undergoing breast surgery , patient in this group will receive an ultrasound guided pectoral nerve block using

Sponsors

Mahatma Gandhi Institute of Medical Sciences Sevagram
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) American society of Anesthesiology 1 and 2 2) patient more than 18 year 3)weight more than 35 kg

Exclusion criteria

Exclusion criteria: 1) The patient refused to undergo the study procedure. 2) The patient has a history of allergies to drugs or drug components used in the study. 3) The patient has a history of neurological deficits. 4) Patients with opioid dependence or addiction are excluded. 5) Patients with American Society of Anesthesiologists physical status classification III or IV are excluded. 6) Patients who took analgesics within 24 hours prior to induction are excluded. 7) Patients with infections at the site of injection are excluded. 8) Patients with inherited or acquired coagulopathies are excluded. 9) Patients on systemic anticoagulation therapy are excluded. 10) Patients with a BMI over 40 are excluded. 11) Patients with psychiatric disorders are excluded.

Design outcomes

Primary

MeasureTime frame
To evaluate and compare Total TRAMADOL consumption in the first 24 hours between two groups of patients who are undergoing breast malignancy surgeries under general anesthesia (GA) with either Erector Spinae Plane block or Modified Pectoral nerve block. Timepoint: AFTER 24 hours

Secondary

MeasureTime frame
To calculate VAS score To check additional analgesia requirementTimepoint: To check any side effects of procedure

Countries

India

Contacts

Public ContactDr Akash Parashram Garkal

Mahatma Gandhi Institute of Medical Sciences, Sevagram

dhirajbhandari@mgims.ac.in9970195086

Outcome results

None listed

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