Autopsy report · NCT03043430
Intranasal Ketamine for Anxiolysis in Pediatric Emergency Department Patients
Cause of deathDrug or device supply
“Research manpower shortage”
Life of this trial
- Registered 8 months after it had already started.
- Ran for about 6 years 11 months before it stopped.
- 10 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Brooke Army Medical Center
- Sponsor type
- US federal agency
- Conditions
- Anxiety; Pediatric ALL; Procedural Anxiety
- Interventions
- Ketamine 100 MG/ML; Midazolam 5 MG/ML
- Participants
- 10
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Does Ultrasound of the Spine Improve Labor Epidurals/Spinal Anesthesia in Obstetric Patients?
“Lack of personnel/research time” - The Role of Ursodeoxycholic Acid in Treatment of Gallstones in Hemolytic Disorders
“Study not feasible - very low recruitment rate” - Selective Attention in Alcohol Use Disorder
“study not funded / no manpower” - Early Integration of Palliative Care in Esophageal Cancer Patients
“Study futility with regards to recruitment” - Feasibility of Using Depth-of-sedation Measuring Equipment (BIS) to Guide Awake Fibreoptic Intubation
“Difficulty in Recruitment due to lack of investigators and suitable patients”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.