WHO ICTRP trial
Comparison of safety and efficacy of propofol/fentanyl in pediatrics emergency…
IRCT20250525065887N1 · Iranian Registry of Clinical Trials (IRCT) · Recruiting
Key facts
| Trial ID | IRCT20250525065887N1 |
|---|---|
| Public title | Comparison of safety and efficacy of propofol/fentanyl in pediatrics emergency department |
| Scientific title | Comparison of safety and efficacy of propofol/fentanyl and midazolam/fentanyl for procedural sedation |
| Primary sponsor | Shahid Beheshti University of Medical Sciences |
| Registry | Iranian Registry of Clinical Trials (IRCT) |
| Recruitment status | Recruiting |
| Study type | interventional |
| Phase | 2 |
| Countries | Iran (Islamic Republic of) |
| Conditions | Condition 1: Patients requiring LP. Condition 2: Patients requiring intubation. Condition 3: Patients with limb dislocation or fracture. Other reaction to spinal and lumbar puncture Respiratory disorder, unspecified Dislocation, sprain and… |
| Interventions | Intervention 1: Intervention group: In the first intervention group, intravenous fentanyl (1–2 micrograms per kilogram) will be administered first, followed by slow intravenous administration of propofol (1–2 milligrams per kilogram). If… |
| Registration date | May 28, 2025 |
| Target size | 84 |
| Registry page | irct.behdasht.gov.ir |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: