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Comparison of two techniques of pain relief in breast surgeries

A comparative study of analgesic efficacy of ultrasound guided serratus anterior plane block versus conventional thoracic paravertebral block for modified radical mastectomy under general anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025288
Enrollment
78
Registered
2020-05-21
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: Ultrasound guided Serrstus Anterior Plane Block: Dose - 20ml of 0.5% Bupivacaine Frequency - Single shot Route 0f administration - Infiltration Control Intervention1: Conventional Thora

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Randomly selected female patients admitted in surgery ward with carcinoma of breast planned for modified radical mastectomy without axillary lymph node dissection belonging to ASA status I or II, aged from 18-60 years willing to give written consent

Exclusion criteria

Exclusion criteria: a)Patient refusal to give consent b)Patients with morbid obesity (body mass index > 40 kg/m2) c)Patients with evidence of peripheral neuropathy, neurological deficit or motor weakness d)Patients with significant cardiac, respiratory, psychiatric, hepatic or renal disorders or any other uncontrolled systemic illness e)Bleeding diatheses or anticoagulation medication intake f)History of pneumothorax g)Pregnant and breast feeding women h)History of allergy to amide local anaesthetics i)Those receiving long term analgesic therapy(daily use > 4 weeks) or a history of opioid dependence j)Infection at the site of block k)History of seizures l)Inability to communicate with the hospital staff

Design outcomes

Primary

MeasureTime frame
Duration 0f post-operative analgesiaTimepoint: Baseline - at extubation, 4th, 6th, 12th, 24th postoperative hours

Secondary

MeasureTime frame
Block Execution TimeTimepoint: Duration in minutes;Diastolic Blood PressureTimepoint: Baseline Just before intubation At 10minutes after induction At 30 Minutes At 60 Minutes At 120 Minutes At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour;Heart RateTimepoint: Baseline Just before intubation At 10minutes after induction At 30 Minutes At 60 Minutes At 120 Minutes At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour ;Mean Blood PressureTimepoint: Baseline Just before intubation At 10minutes after induction At 30 Minutes At 60 Minutes At 120 Minutes At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour ;Morphine ConsumptionTimepoint: At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour;Systolic Blood PressureTimepoint: Baseline Just before intubation At 10minutes after induction At 30 Minutes At 60 Minutes At 120 Minutes At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour ;VAS scoreTimepoint: At extubation At 4th postoperative hour At 6th postoperative hour At 12th postoperative hour At 24th postoperative hour

Countries

India

Contacts

Public ContactDr Chiranjib Bhattacharyya

Department of Anaesthesiology IPGME&R and SSKM hospital

bhattach1@yahoo.com9433508030

Outcome results

None listed

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