Comparasion between Serratus Posterior Superior Intercostal block and Erector Spinae block in children for pain ttreatment

Comparative study of Continuous Serratus Posterior Superior Intercostal plane block with Continuous Erector Spinae Plane Block in Pediatric 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/2025/10/095763

Enrollment

Registered

2025-10-09

Start date

Unknown

Completion date

Unknown

Last updated

2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J708- Respiratory conditions due to other specified external agents

Interventions

Intervention1: continuous serratus posterior superior plane block: will receive continuous serratus superior plane block after general anaesthesia. Dose :.0.5 ml/kg of 0.125% bupivacaine will be given

Eligibility

Inclusion criteria

Inclusion criteria: ASA I/II Scheduled for the right or left thoracotomy surgery

Exclusion criteria

Exclusion criteria: Any coagulation abnormality Raised intracranial pressure Deformity of the thoracolumbar spine Local infection at the site of catheter placement

Design outcomes

Primary

Measure	Time frame
To compare 24 hour Post-operative Fentanyl consumptionsTimepoint: 24 hour	—

Secondary

Measure	Time frame
Time of first rescue analgesia required FLACC score postoperative period at 30 min, 2 hour, 4 hour, 8 hour, 12 hour, 24 hour Adverse effect like pneumothorax, nausea, vomiting Timepoint: 24 hour	—

Countries

India

Contacts

Public ContactDR POONAM KUMARI

All India Institute of Medical Sciences,Patna

drpoonam1981@gmail.com9473199126

Outcome results

None listed

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