TerminatedN/AOther

Techniques to Reduce the Severity and Frequency of Emergent Reactions

Sponsored by CHRISTUS Health

NCT ID
NCT03832309
Target Enrollment
38 participants
Start Date
2017-11-21
Est. Completion
2021-06-21

About This Study

The objectives of this study are first to determine if the power of suggestion will decrease the frequency and severity of emergence reactions after procedural sedation and analgesia with ketamine in the setting of the emergency department. Second, to determine if people dream about what they were thinking about when they were induced with ketamine.

Conditions Studied

Analgesia

Interventions

  • Do we speak to them in a way that convinces them to have the dream
  • Speaking to them as a regualar person

Eligibility

Age:18 Years - N/A
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Be at least 18 years of age
* Required need for procedural sedation and analgesia

Exclusion Criteria:

* Age\< 18
* Hypertension
* Raised Intracranial pressure
* Major psychological disorders
* Procedures involving laryngel manipulations
* History of Laryngeal sapsm History of adverse reactions to ketamine

Study Locations (1)

CHRISTUS Health
Corpus Christi, Texas, United States

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source