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Comparision of two commonly used drugs Injection Dexmedetomidine and Injection Fentanyl as adjuvant in Caudal Analgesia for pain relief in Paediatric Cardiac Surgery.

COMPARATIVE STUDY OF EFFECT OF CAUDAL DEXMEDETOMIDINE Vs CAUDAL FENTANYL ON HEMODYNAMIC RESPONSE AND POSTOPERATIVE PAIN IN PAEDIATRIC CARDIAC SURGERY PATIENTS ?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051255
Enrollment
60
Registered
2023-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: Q212- Atrioventricular septal defect Health Condition 2: - Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Injection Dexmedetomidine in Caudal Analgesia: Single shot Injection Dexmedetomidine 0.5 microgram/kg in Caudal route. Duration of intervention - 20 minutes Control Intervention1: Injec

Sponsors

Research cell JNMC Sawangi Wardha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Atrial septal defect or ventricular septal defect undergoing intracardiac repair on Cardiopulmonary bypass Weighing 5-15 kg

Exclusion criteria

Exclusion criteria: Patients with multiple cardiac defects, Coagulation abnormalities, Infection at caudal injection site, Any patient receiving sedation Within 24 hours of surgey.

Design outcomes

Primary

MeasureTime frame
Hemodynamic response and Postoperative painTimepoint: Hemodynamic Baseline and Intraoperative at specific events - After sternotomy, after bypass ,extubation and in ICU after shifting Pain Score - In ICU for First 8 hours—

Secondary

MeasureTime frame
ICU stay, Time to extubationTimepoint: Duration of stay in ICU - 48 hours, 72 hours ; Time of extubation 2 hours,4 hours, 6 hours after surgery—

Countries

India

Contacts

Public ContactDr Roshani Manwani

Jawaharlal Nehru Medical College, Sawangi , Wardha

dhawal104@gmail.com8779013650

Outcome results

None listed

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