CompletedPhase 4ketamine

Ketamine-propofol Versus Ketamine Alone for Procedural Sedation in Adults

Sponsored by Centre Hospitalier Universitaire de Nice

NCT ID
NCT01544725
Target Enrollment
150 participants
Start Date
2012-04
Est. Completion
2016-01

About This Study

Using Ketamine for procedural sedation in adults is often uncomfortable for emergency physicians because of the significant proportion of patients experimenting recovery agitation. The investigators believe that combining propofol to ketamine, the proportion of recovery agitation will be significantly lowered. The objectives of this double-blinded, randomized controlled trial are to compare the proportion of recovery agitation in adults receiving procedural sedation with ketamine-propofol versus ketamine alone, and to compare the proportion of other classical procedural sedation side-effects and parameters such as respiratory depression, hypotension, sedation duration, time of recovery, procedural failures, and levels of satisfaction.

Conditions Studied

FractureDislocation

Interventions

  • Procedural sedation with ketamine-propofol combination
  • Procedural sedation with ketamine alone

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* 18 years and older
* indication of procedural sedation

Exclusion Criteria:

* allergy to propofol or ketamine
* alcohol or drug intoxication
* altered mental status
* ASA physical status score \> 2
* hemodynamic unstability

Study Locations (1)

Hôpital St Roch
Nice, France

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source