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Comparison of two different methods for pain relief, namely Serratus Anterior Plane Block and Caudal Epidural, in pediatric patients undergoing heart surgery

Comparative effects of Serratus Anterior Plane Block and Caudal Epidural on Post Thoracotomy Pain in Pediatric patients : A Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042075
Enrollment
74
Registered
2022-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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: Serratus Anterior Plane Block: Serratus Anterior Plane Block will be performed in the operating room after induction of anesthesia using the USG machine. Patient will be placed in a lat

Sponsors

PGIMER Post Graduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pediatric patients aged between 6 months to 7 years 2. Pediatric patients undergoing surgery requiring thoracotomy e.g., PDA ligation, coarctation of aorta, lung resection surgery etc. 3. ASA I or II

Exclusion criteria

Exclusion criteria: 1. Patient on anticoagulation or bleeding disorder 2. Contraindications for Regional Anesthesia - Local site infection, allergy to local anesthetics, consent refusal 3. Preoperative lung consolidation, mechanical ventilation, severe LV dysfunction or, anticipated need for postoperative mechanical ventilation more than 6-8hrs 4. Pre-Existing severe renal or hepatic insufficiency 5. Patients requiring sternotomy for their surgery

Design outcomes

Primary

MeasureTime frame
Total analgesic requirement in 24hrs. Timepoint: 24hrs

Secondary

MeasureTime frame
1. To compare the amount of intraoperative analgesic and anesthetic requirement 2. To compare post-operative pain by using FLACC scale 3. To compare time to 1st rescue analgesia 4. To compare the safety of interventions by assessing critical events such as hypotension, bradycardia, and respiratory depression.Timepoint: 24hrs

Countries

India

Contacts

Public ContactDr Himanshu Punetha

PGIMER, Chandigarh

bhupeshkr@yahoo.com7087009511

Outcome results

None listed

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