ACTRN12615001151527
Terminated
Phase 3
Double blind randomised controlled study to compare the usual practice of additional opiates with iv ketamine in unselected emergency patients complaining of moderate to severe pain despite already receiving opiate analgesia.
Bundaberg Base Hospital0 sites23 target enrollmentOctober 29, 2015
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Bundaberg Base Hospital
- Enrollment
- 23
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients reporting acute onset of pain of any cause except cardiac origin but including cases where the cause is unknown. A verbal numeric rating scale pain score of greater than or equal to 5 after having received a total intravenous dose of 7\.5mg morphine, 100mcg fentanyl or other equipotent opiate.
Exclusion Criteria
- •Patients whose primary language is other than English
- •Women who are pregnant
- •Patients aged \<18 years
- •Patients with intellectual or mental impairment
- •A patient in whom we are unable to gain venous access
- •Patients with known chronic kidney disease stage 4 or above
- •Acute severe respiratory distress
- •Presenting with presumed cardiac diagnosis
- •A documented allergy to morphine or ketamine
Outcomes
Primary Outcomes
Not specified
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