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Comparison of pain relief and Safety of Continuous Epidural medication versus Local Infiltration and intravenous medicines in video assisted Decortication in children with Empyema

Comparison of Analgesic Efficacy and Safety of Continuous Epidural Infusion versus Local Infiltration and Systemic Opioids in VATS Decortication in Paediatric Empyema Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/07/008968
Enrollment
30
Registered
2017-07-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: null- PAEDIATRIC PATIENTS WITH EMPYEMA

Interventions

Intervention1: GROUP E i.e. EPIDURAL: In group E patients, a thoracic epidural catheter was inserted between T4 and T8.Test dose of 1% adrenalized lignocaine 0.1 ml/kg was given to rule out intravascu

Sponsors

Department of Anaesthesia Seth GS medical college KEM hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients in the age group one to twelve years posted for VATS decortication for empyema thoracis

Exclusion criteria

Exclusion criteria: Patients with contraindications for regional anaesthesia i.e., local sepsis at the site of insertion, coagulopathy, severe valvular heart disease, patient/parental refusal, and known allergy to local anesthetic agents

Design outcomes

Primary

MeasureTime frame
The analgesic efficacy will be assessed using the FLACC scale for preverbal childreni.e.1 – 3years and the Wong Baker Faces scale for more than 3 years of age.Timepoint: The pain scores will be assessed at interval of 4 hours on the first day and at interval of 6 hours on the second day

Secondary

MeasureTime frame
SAFETY. Side effects like motor blockade, nausea and vomiting, constipation, urinary retention, respiratory depression, toxicity of local anaesthetics, pruritus, infection at catheter site, etc will be looked for.Timepoint: The side effects will be assessed at interval of 4 hours on the first day and at interval of 6 hours on the second day

Countries

India

Contacts

Public ContactDr Nandini Dave

Department of Anaesthesia, Seth G.S. medical college, K.E.M. hospital,

nandinidave@gmail.com9819392094

Outcome results

None listed

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