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RCT for Intermittent Versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies

NCT00515359 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 276

Last updated 2024-01-19

No results posted yet for this study

Summary

RCT for Intermittent versus Continuous Propofol Sedation for Pediatric Brain and Spine MRI Studies

Conditions

  • Encephalopathy
  • Developmental Delay and Behavioral Changes
  • Cord Tumor Compression or Instability
  • Cord Tethering or Malformation

Interventions

PROCEDURE

Intermittent Propofol Sedation

Intermittent versus continuous dosage

PROCEDURE

Continuous Propofol Sedation

intermittent vs continuous dosage

Sponsors & Collaborators

  • Helen DeVos Children's Hospital

    collaborator OTHER

  • Spectrum Health Hospitals

    lead OTHER

Principal Investigators

  • Nabil Hassan, MD · Helen DeVos Children's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Month
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2009-02-28
Completion
2009-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00515359 on ClinicalTrials.gov