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To observe and compare the effect of injection of a drug ( medicine) at two different sites in between muscles for pain relief in patients who undergo breast cancer surgery.

Comparison of ultrasound-guided erector spinae plane block with serratus anterior muscle block in patients undergoing modified radical mastectomy- A randomized control trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018067
Enrollment
80
Registered
2019-03-13
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: Group E- Erector spinae plane block. : Ipsilateral ultrasound guided Erector spinae plane block with 20 ml of 0.25% ropivacaine in patients undergoing modified radical mastectomy after

Sponsors

Department of Anaesthesia and Intensive care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Females suffering from carcinoma breast. 2.American Society of Anaesthesiologists status I-II 3.Age ranging from 18-80 years

Exclusion criteria

Exclusion criteria: 1.Patient refusal. 2.History of relevant drug allergy. 3.History of psychiatric illness and substance abuse. 4.Patient suffering from severe cardiovascular, respiratory,liver, metabolic or neurological disease. 5.Chronic treatment with analgesics. 6.Pregnant patient. 7.Coagulopathy. 8.Infection at planned injection site. 9.Psychological inability of the patient to understand and interpret visual analogue scale.

Design outcomes

Primary

MeasureTime frame
To evaluate the reduction in pain intensity in post-operative period by using linear visual analogue scale (VAS) score in patients receiving either ESP block or SAM block following MRM.Timepoint: Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs.

Secondary

MeasureTime frame
1.Morphine consumption over 24 hrs 2.Total dose of antiemetics over 24 hours. 3.Safety profile of both the blocks. 4.Changes in hemodynamic variables. 5.Side effects pertaining to the procedure or drugs.Timepoint: 1.Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs. 2.Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs. 3.Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs. 4.Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs. 5.Post-operative at 30 mins,1 hr,4 hrs,8 hrs,12 hrs and 24 hrs.

Countries

India

Contacts

Public ContactDr Richa Saroa

Government Medical College and Hospital, Chandigarh

sanjeev_palta@yahoo.com9646121523

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 9, 2026