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Comparison between Serratus Posterior Superior Intercostal plane block and Epidural for the treatment of pain in young patient in chest operation

Comparative study of Continuous Serratus Posterior Superior Intercostal plane block With Thoracic Epidural in adult patients for postoperative analgesia in thoracotomy: A randomised control trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/078970
Enrollment
44
Registered
2025-01-20
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: J65- Pneumoconiosis associated with tuberculosis

Interventions

Intervention1: Continuous Serratus Posterior Superior Plane Block: continuous serratus posterior superior plane block given with 0.125%bupivacaine according to the dermatomal coverage Postoperative pe

Sponsors

All India institute of Medical SciencesPatna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I/II Scheduled for thoracotomy surgery

Exclusion criteria

Exclusion criteria: Mental disorder Communication failure Inability to understand the functionality of patient-controlled analgesia pump

Design outcomes

Primary

MeasureTime frame
To compare 24 hour Postoperative Local anaesthestic consumptionTimepoint: 24 hour—

Secondary

MeasureTime frame
1.Time of first rescue analgesic required 2.Intra operative opioid (fentanyl) consumption 3.Total opioid (fentanyl) consumption in 24-hour postoperative period 4.NRS score: postoperative period at 30 min, 2 hour, 4 hour, 8 hour, 12 hour, 24 hour at rest & movement 5.Adverse effect : Hypotension, Bradycardia, Pneumothorax, Nausea vomiting Timepoint: 30 min, 2 hour, 4 hour, 8 hour, 12 hour, 24 hour—

Countries

India

Contacts

Public ContactPoonam Kumari

All India Institute of Medical Sciences,Patna

drpoonam1981@gmail.com9473199126

Outcome results

None listed

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