# Ketofol Versus Fentofol for Procedural Sedation in the Pediatric Emergency Department

> **NCT02079090** · PHASE3 · COMPLETED · sponsor: **University of British Columbia** · enrollment: 30 (actual)

## Conditions studied

- Emergency Department Procedural Sedation
- Fracture Reduction

## Interventions

- **DRUG:** Ketofol
- **DRUG:** Fentofol

## Key facts

- **NCT ID:** NCT02079090
- **Lead sponsor:** University of British Columbia
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2014-07
- **Primary completion:** 2017-06
- **Final completion:** 2017-06
- **Target enrollment:** 30 (ACTUAL)
- **Last updated:** 2017-10-27

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02079090

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02079090, "Ketofol Versus Fentofol for Procedural Sedation in the Pediatric Emergency Department". Retrieved via AI Analytics 2026-05-29 from https://api.ai-analytics.org/clinical/NCT02079090. Licensed CC0.

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