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
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Do we speak to them in a way that convinces them to have the dream | During induction, and depending on what group they are randomized to, the physician will speak to them about having a dream while on the drug |
| BEHAVIORAL | Speaking to them as a regualar person | During 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.