WHO ICTRP trial
Comparing the effectiveness of two different medication regimen for sedating…
CTRI/2024/06/068952 · Clinical Trials Registry India (CTRI) · Not Recruiting
Key facts
| Trial ID | CTRI/2024/06/068952 |
|---|---|
| Public title | Comparing the effectiveness of two different medication regimen for sedating patients with severe injury to the brain due to trauma who have been admitted in ICU |
| Scientific title | A prospective randomized blinded controlled trial on the efficacy of Propofol-Fentanyl versus Ketamine-Dexmedetomidine sedation in patients with severe traumatic brain injury admitted in trauma intensive care - NIL |
| Primary sponsor | Department of Anesthesia and Intensive Care |
| Registry | Clinical Trials Registry India (CTRI) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Phase | Phase 3 |
| Countries | India |
| Conditions | Health Condition 1: S069- Unspecified intracranial injury |
| Interventions | Intervention1: Group Ketamine/ Dexmedetomidine (KD): Agent: Intravenous infusion of Ketamine at 1-5mg/kg/hr and Dexmedetomidine at 0.3-0.75 mcg/kg/hr for 48 hours Control Intervention1: Group Propofol/Fentanyl (PO): Agent: Intravenous… |
| Registration date | Jun 14, 2024 |
| Target size | 52 |
| Secondary IDs | NIL |
| Registry page | ctri.nic.in |
At a glance
- No Results available
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: