Status:

COMPLETED

Patient Satisfaction With Subdissociative Dose Ketamine Versus Morphine for Emergency Department Pain Control

Lead Sponsor:

CHRISTUS Health

Conditions:

Abdominal Pain

Eligibility:

All Genders

18+ years

Brief Summary

The proposed research will be a single blinded (patient) randomized controlled prospective trial of adult patients receiving treatment for moderate to severe abdominal pain to test the hypothesis that...

Detailed Description

Informed consent will be obtained from patients presenting with chief complaint of moderate to severe abdominal pain in the emergency department who do not meet any exclusion criteria and who willingl...

Eligibility Criteria

Inclusion

  • Be at least 18 years of age
  • Initial presenting complaint of moderate to severe abdominal pain (five or higher on numerical rating scale \[NRS\]).
  • Subjects will be enrolled into the project one (1) time only.

Exclusion

  • Under 18 years of age
  • Pregnant patients
  • Inability to provide written consent
  • Evidence of traumatic brain injury
  • Hemodynamic instability
  • Procedures involving laryngeal manipulation
  • History of laryngeal spasm
  • History of adverse reaction to Ketamine or morphine
  • Patients will not be excluded if they had received pain medications prior to enrollment (ie. Received pain medication from triage, non-physician provider (NPP), or emergency medical services (EMS) prior to being seen by physician
  • History of opioid use in the last week, prescription opioid use, recreational opioid use

Key Trial Info

Start Date :

December 19 2019

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 16 2020

Estimated Enrollment :

32 Patients enrolled

Trial Details

Trial ID

NCT04698772

Start Date

December 19 2019

End Date

November 16 2020

Last Update

January 7 2021

Active Locations (1)

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CHRISTUS

Corpus Christi, Texas, United States, 78404