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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02145169
Other study ID # HN4507FBD
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2013
Est. completion date April 2016

Study information

Verified date December 2016
Source Albert Einstein Healthcare Network
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To describe the safety and efficacy of nitrous oxide during ketamine administration for the prevention of emergence reaction during Emergency Department procedural sedation and analgesia in adults. Drugs such as fentanyl, midazolam, and propofol are widely used in emergency departments for procedural sedation and analgesia because they have a rapid onset and short duration of action. Unfortunately, all of these agents may cause respiratory depression, particularly when combined with other sedative agents, administered in large doses, or given to patients with underlying respiratory diseases. Nitrous oxide use during ketamine administration may be an ideal combination for the prevention of emergence reaction in adults sedated in the ED. Like ketamine, nitrous oxide has an excellent cardio-respiratory profile as well as some analgesic and anxiolytic qualities. The anxiety and pain surrounding procedural sedation is not limited to the procedure itself, but the elapsed time from the time the patient enters the ED to the time spent in preparation for the procedure can be significant and lead to increased anxiety, which may exacerbate emergence reactions in adults. Using nitrous oxide before ketamine administration may mitigate this. While midazolam has shown efficacy in reducing emergence reactions in adults sedated with ketamine, the investigators believe that inhaled nitrous oxide may be equivalent to midazolam, with a better cardio-respiratory profile.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Inhaled Nitrous Oxide
Patients undergoing procedural sedation with Ketamine will receive inhaled Nitrous Oxide

Locations

Country Name City State
United States Albert Einstein Healthcare Network Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Albert Einstein Healthcare Network

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Emergence Reaction Presence or absence of emergence reaction At primary ED visit when the patient is undergoing the intervention
Secondary Physiologic Measure ETCO2 measured q 5 seconds At primary ED visit when the patient is undergoing the intervention
Secondary Physiologic Measure SpO2 measured q 5 seconds At primary ED visit when the patient is undergoing the intervention
Secondary Vitals heart rate, respiratory rate, peripheral SaO2 At primary ED visit when the patient is undergoing the intervention
Secondary Physician Interventions verbal or physical stimulation, airway repositioning, additional oxygen, positive pressure ventilation, endotracheal intubation At primary ED visit when the patient is undergoing the intervention
Secondary Level of Sedation Ramsay sedation score At primary ED visit when the patient is undergoing the intervention
Secondary Patient Recall of Procedure Patient recall of procedure At primary ED visit when the patient is undergoing the intervention
Secondary Total Ketamine Dose Total Ketamine dose At primary ED visit when the patient is undergoing the intervention
Secondary Total Time of Nitrous Use Total elapsed time of nitrous use At primary ED visit when the patient is undergoing the intervention
Secondary Physician Procedure Satisfaction Score Physician procedure satisfaction survey responses At procedure completion
Secondary Patient Procedure Satisfaction Score Patient procedure satisfaction survey responses At procedure completion
Secondary Nurse Procedure Satisfaction Score Nurse procedure satisfaction survey responses At procedure completion
Secondary Length of ED Stay Length of ED stay At primary ED visit
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