Clinical Trials Directory

Trials / Terminated

TerminatedNCT03832309

Techniques to Reduce the Severity and Frequency of Emergent Reactions

Non-Pharmacological Techniques to Reduce the Severity and Frequency of Emergency Reactions After Procedural Sedation and Analgesia in the Emergency Department

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
CHRISTUS Health · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

The proposed research will be single blinded (patient) randomized controlled trial with a retrospective component to test the hypothesis that the power of suggestion will reduce the frequency and severity of emergence reactions, even in the setting of the emergency department. The study will be conducted in the emergency department at CHRISTU Spohn Shoreline Hospital. CHRISTUS Spohn Shore hospital is the region's primary acute care center. It houses the Chest Pain, Stroke, and Cancer Centers of CHRISTUS Spohn, and the only level II trauma center in south Texas. It is a major teaching affiliate of Texas A\&M medical school, and serves an inner-city population.

Conditions

Interventions

TypeNameDescription
BEHAVIORALDo we speak to them in a way that convinces them to have the dreamDuring induction, and depending on what group they are randomized to, the physician will speak to them about having a dream while on the drug
BEHAVIORALSpeaking to them as a regualar personDuring induction, if the patient is in group 1, the resident performing procedural sedation will remind the patient about what the patient wanted to dream and ask them to focus on that as the ketamine is being administered. If the patient is in group 2, the resident performing procedural sedation will give no specific instruction to the patient at this point.

Timeline

Start date
2017-11-21
Primary completion
2021-06-21
Completion
2021-06-21
First posted
2019-02-06
Last updated
2022-04-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03832309. Inclusion in this directory is not an endorsement.