# Comparison of Propofol to Precedex With Propofol for Emergence and Recovery in Patients Having Craniotomy Surgery

> **NCT00848991** · PHASE3 · COMPLETED · sponsor: **The Cooper Health System** · enrollment: 15 (actual)

## Conditions studied

- Cranitomy Surgery

## Interventions

- **DRUG:** Precedex
- **DRUG:** Propofol

## Key facts

- **NCT ID:** NCT00848991
- **Lead sponsor:** The Cooper Health System
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2009-02
- **Primary completion:** 2010-02
- **Final completion:** 2010-02
- **Target enrollment:** 15 (ACTUAL)
- **Last updated:** 2012-02-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00848991

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00848991, "Comparison of Propofol to Precedex With Propofol for Emergence and Recovery in Patients Having Craniotomy Surgery". Retrieved via AI Analytics 2026-06-04 from https://api.ai-analytics.org/clinical/NCT00848991. Licensed CC0.

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