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An observational study to compare two pain relief methods after breast surgery an intravenous drug and a regional nerve block injection ,to see which one has a longer pain relief effect post surgery

Comparison of Erector Spinae Plane block and Intravenous Dexmedetomidine for postoperative pain relief in patients undergoing breast surgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/103892
Enrollment
74
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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: Nil: Nil

Sponsors

Dr Simran Shetty
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: 1)Female patients aged between 18-75 years 2)Elective mastectomy surgery under general anaesthesia. 3)American society of anaesthesiologists class I - II patients.

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA: 1)Patient refusal. 2)Pregnant patients. 3)Patients with psychiatric diagnosis/cognitive dysfunction 4)Surgical duration more than 6 hrs

Design outcomes

Primary

MeasureTime frame
Primary Outcome 1)Duration of post operative analgesia 2)Post operative Visual Analogue scale ( VAS score ) Timepoint: 1. The data for duration of post operative analgesia and post operative visual analogue scale for each sample will be collected by then end of 24 hrs. 2. Correlation of data will be done after complete data collection - 1 year from the time of ethics committee approval

Secondary

MeasureTime frame
1. Requirement of rescue analgesia 2. RSS ( Ramsay Sedation Scale) sedation score 3. Hemodynamic parameters Heart Rate , Systolic Blood Pressure , Diastolic Blood pressure , Respiratory Rate , Saturation Timepoint: The secondary outcome data for each sample will be collected by the end of 24 hrs. Correlation of data will be done after complete data collection - 1 year from the time of ethics committee approval

Countries

India

Contacts

Public ContactDr Simran Shetty

Kasturba Medical College , Mangalore

drranjanrao@gmail.com9449837154

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026