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Triclofos Sodium VS Intravenous Dexmedetomidine-Ketamine For Sedation in Children For Magnetic Resonance Imaging

Comparison Of Efficacy Of Oral Triclofos Sodium VS Intravenous Dexmedetomidine -Keatamine For Sedation in Children undergoing Magnetic Resonance Imaging - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075137
Enrollment
140
Registered
2024-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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: Oral Triclofos Sodium: Dose - 100 mg/kg Route of administration - orally in syrup form Control Intervention1: Inj Dexmedetomidine-Ketamine: Dose - Inj. Dexmedetomidine 1 microgram/kg an

Sponsors

Khyati C Jethva
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2, Pediatric Patients age 6 months to 5 years, weight 5to18kg, Elective MRI

Exclusion criteria

Exclusion criteria: Congenital Heart Disease Liver/Kidney/Systemic/Metabolic Disease Anticipated Difficult Airway and Allergy to Study Drug

Design outcomes

Primary

MeasureTime frame
Ramsay Sedation score in Children undergoing MRITimepoint: Upto 6 hour from giving study drug

Secondary

MeasureTime frame
1. Hemodynamics parameters (HR,RR,Spo2) 2. Onset of sedation, duration of sedation & total recovery time from sedation 3. the need for supplementation of rescue dose 4. Quality of MRI 5. Adverse effect of study drugTimepoint: 1.Hemodynamics parameters(HR,RR,Spo2)-120 mins 2.Onset of sedation, Duration of sedation & total recovery time from sedation- 6 hours 3. Need for supplementation of rescue dose- 1st,2nd,3rd dose, total dose. 4.Quality of MRI- Grade 1,2,3 5.Adverse effects of drugs- 6 hours

Countries

India

Contacts

Public ContactMayurika J Patel

PDU Medical College, Rajkot

khyatijethva13@gmail.com9913732613

Outcome results

None listed

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