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Active Not RecruitingNCT04801589

Sedation approaches for ventilated infants and children

About this titleRead the official source — NCT04801589
Medication studyAges 44 weeks–11 yearsUnited StatesPTSD
The study in practice

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Who could participate?

Listed age limits: 44 weeks to 11 years.

Listed locations
NashvilleSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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What to know before participating

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This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

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Study start dateStarted: May 10, 2021
Recruitment status
Active Not Recruiting
Enrollment listed in the registry
372
Sponsor
Vanderbilt University Medical Center
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 44 Weeks to 11 Years
Official registry ID
NCT04801589
Official title
Show the full official title

Maximizing Efficacy of Goal-Directed Sedation to Reduce Neurological Dysfunction in Mechanically Ventilated Infants and Children Study

Recruitment & locations

Not recruiting

Nashville

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Vanderbilt University Medical Center, a hospital or academic medical center.

Does this study involve medication?

Yes. The study involves medication, including Dexmedetomidine and Midazolam.

Who can participate?

Listed age limits: 44 weeks to 11 years.

Is this study still recruiting?

The registry lists this study as active, but no longer recruiting.

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