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USG guided PEC block for chest wall surgeries

Post operative analgesia in chest wall surgeries : Implications of USG guided PEC block

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033046
Enrollment
100
Registered
2021-04-23
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: O- Medical and Surgical

Interventions

Intervention1: USG guided PEC block: USG guided PEC block for Postoperative analgesia Control Intervention1: USG Guided Pec block, comparison of ropivacaine and ropivacaine with fentanyl Group R : 0.2

Sponsors

GCS MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective unilateral modified radical mastectomy for carcinoma breast after obtaining informed consent Wt 40 to 70 kg Patients undergoing elective breast reconstruction Asa 1,2,3

Exclusion criteria

Exclusion criteria: ASA 4 Male >70 years of age Patients who are refusing to give consent Bilateral breast surgeries Only lumpectomy Surgery duration > 4 hours Carcinoma breast patients with metastasis Patients allergic to local anaesthetics Patients with h/o bleeding diathesis Patients on anticoagulants Patients with deranged liver function tests Â

Design outcomes

Primary

MeasureTime frame
Duration of analgesia ( time of first rescue analgesia after extubation) total cumulative dose of fentanyl (opoid) required for first 24 hours post operatively total cumulative dose of PCM (paracetamol ) required for first 24 hours post operativelyTimepoint: Duration of analgesia ( time of first rescue analgesia after extubation) total cumulative dose of fentanyl (opoid) required for first 24 hours post operatively total cumulative dose of PCM (paracetamol ) required for first 24 hours post operatively

Secondary

MeasureTime frame
any adverse effects such as local anaesthesia toxicity, hemodynamic instability, bradycardia, hypotension , nausea or vomitting , parasthesia, respiratory depression. Hematoma, pneumothorax Timepoint: During first 24 hours

Countries

India

Contacts

Public ContactDr Divya Kheskani

GCS Medical College, Hospital and Research Centre

divya.kheskani@gmail.com8980738209

Outcome results

None listed

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