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To observe the additional pain sparing effect of a drug(tramadol) given as an injection in between two muscles in patients who undergo breast cancer surgery.

Role of tramadol as an adjuvant in ultrasound guided serratus anterior muscle block for modified radical mastectomy - a randomized control trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018146
Enrollment
70
Registered
2019-03-18
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 T- SAM block with tramadol as an djuvant: Ipsilateral ultrasound guided Serratus Anterior Muscle block with ropivacaine 0.25%(18ml) and tramadol 100mg(2ml) in patients undergoing

Sponsors

Department of Anaesthesia and Intensive care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Females diagnosed with carcinoma breast. 2.American Society of Anaesthesiologists physical status 1-2. 3.Age 18-80 years

Exclusion criteria

Exclusion criteria: 1.History of relevant drug allergy. 2.History of psychiatric illness, substance abuse. 3.Severe cardiovascular, respiratory, liver diseases, metabolic or neurological disease. 4.Chronic treatment with analgesics. 5.Pregnancy 6.Coagulopathy 7.Infection at planned injection site. 8.Psychological inability of the patient to understand Visual Analogue Scale.

Design outcomes

Primary

MeasureTime frame
Cumulative morphine consumption over 24 hours in patients receiving SAM block with or without tramadolTimepoint: Post-operative at 30mins,1hr,4hrs,8hrs,12hrs and 24hrs

Secondary

MeasureTime frame
1.Reduction in pain intensity by VAS score. 2.Total dose of anti-emetics over 24hrs. 3.Changes in haemodynamic variables. 4.Any side effects pertaining to the procedure or drugs.Timepoint: 1.Post-operative at 30mins,1hr,4hrs,8hrs,12hrs and 24hrs. 2.Post-operative at 30mins,1hr,4hrs,8hrs,12hrs and 24hrs 3.Post-operative at 30mins,1hr,4hrs,8hrs,12hrs and 24hrs 4.Post-operative at 30mins,1hr,4hrs,8hrs,12hrs and 24hrs

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 4, 2026