Status:
TERMINATED
Techniques to Reduce the Severity and Frequency of Emergent Reactions
Lead Sponsor:
CHRISTUS Health
Conditions:
Analgesia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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 ...
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 seve...
Eligibility Criteria
Inclusion
- Be at least 18 years of age
- Required need for procedural sedation and analgesia
Exclusion
- Age\< 18
- Hypertension
- Raised Intracranial pressure
- Major psychological disorders
- Procedures involving laryngel manipulations
- History of Laryngeal sapsm History of adverse reactions to ketamine
Key Trial Info
Start Date :
November 21 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 21 2021
Estimated Enrollment :
38 Patients enrolled
Trial Details
Trial ID
NCT03832309
Start Date
November 21 2017
End Date
June 21 2021
Last Update
April 6 2022
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
CHRISTUS Health
Corpus Christi, Texas, United States, 78404