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Use of Clonidine to Prevent Withdrawal Following Prolonged Dexmedetomidine Infusions

J

Joseph D. Tobias

Status

Completed

Conditions

Sedation

Treatments

Drug: Clonidine

Study type

Observational

Funder types

Other

Identifiers

NCT02404077
IRB15-00256

Details and patient eligibility

About

The investigators' clinical practice makes use of oral clonidine as a means of transitioning from intravenous dexmedetomidine following prolonged infusions (more than 3-5 days). Although this is common clinical practice, there is limited clinical data to demonstrate the efficacy of this technique and to provide clonidine dosing guidelines. The purpose of this study is to retrospectively review the investigators' experience with the use of oral clonidine to prevent withdrawal following the prolonged administration of dexmedetomidine.

Enrollment

712 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who received clonidine during the transition from dexmedetomidine.

Exclusion criteria

  • None

Trial design

712 participants in 1 patient group

Clonidine
Description:
Patients who received clonidine following prolonged dexmedetomidine infusions
Treatment:
Drug: Clonidine

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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