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Comparison of pain relief with injection given on upper back versus without injection in patients undergoing breast cancer sugery

Erector spinae plane block for postoperative analgesia in modified radical mastectomy: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012307
Enrollment
60
Registered
2018-03-05
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: null- ASA I and II patients Health Condition 2: C509- Malignant neoplasm of breast of unspecified site Health Condition 3: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: erector spinae plane block: Patients in block group will receive usg- guided erector spinae plane block in sitting position with monitoring of NIBP, SPO2, HR with an I.V. line insitu.0.

Sponsors

Department of Anaesthesia and Intensive Care PGIMER Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. 60 ASA (American Society of Anaesthesiologists) I-II female patients in the age group of 18-60 years 2. scheduled to undergo total mastectomy with axillary clearance under general anaesthesia will be enrolled in the study.

Exclusion criteria

Exclusion criteria: 1. Local infection at the block site 2. Coagulopathy 3. Morbid obesity (BMI >40) 4. Allergy to local anaesthetics 5. Uncontrolled hypertension or Ischemic heart disease 6. Renal dysfunction 7. Pre-existing neurological deficits 7. Psychiatric illness

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is to measure analgesic efficacy of erector spinae plane block in terms of morphine consumption in the first 24 hours in patients undergoing total mastectomy and axillary clearance under erector spinae plane block with general anaesthesia and general anaesthesia alone.Timepoint: at 24 hours post operatively total morphine consumption will be recorded

Secondary

MeasureTime frame
The secondary aims are to compare the time to first rescue analgesia, pain scores as assessed by Numerical Rating Scale (NRS) in the two groups and to evaluate the characteristics & complications associated with the block procedure.Timepoint: postoperative period at 0min 30 min 1 hr 2hr 4hr 6hr 8hr 12hr and 24hr

Countries

India

Contacts

Public ContactShashikant sharma

Postgraduate Institute of Medical Education and Research

drsumanarora@hotmail.com7087009528

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 20, 2026