Optimal Timing of Ketamine Initiation for SCD Pain
Starting soon · Phase 3 · Has a placebo group
Conditions studied: Sickle Cell Disease, Sickle Cell Crisis
In brief
The goal of this clinical trial is to learn if the use of early ketamine decreases the chance of admission to the hospital in patients with sickle cell disease presenting with pain. The main questions this study aims to answer are: * Does ketamine given within 1 hour of acute care presentation decrease the chance of hospital admission? * If admitted, does continuing ketamine in the first few hours of admission decrease opioid use or length of stay compared to those who start it later in the admission? Researchers will compare the study arm to patients with sickle cell disease who receive placebo within 1 hour of presentation for the first aim. Participants will be given ketamine/placebo by mouth without 1 hour of presentation. If admitted, all participants will be able to start open label IV ketamine upon admission to the floor based on their clinical needs. Participants who end up starting ketamine will be reviewed to determine if early start to ketamine is helpful in reducing opioid use and length of stay.
Key facts
- Study ID
- NCT07450430
- Run by
- Boston Children's Hospital
- People needed
- 90
- Starts
- 2026-02-01
- Expected to finish
- 2030-02-01
- Last updated by the study team
- 2026-03-09
Who can join
Age: 6 and older, up to 24. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- sickle cell disease diagnosis
- presenting with pain to ED or infusion clinic
- patient at study site
- 6 to 24 years old
You may not qualify if…
- allergy to ketamine
- severe side effects associated with ketamine
- unable to consent
Where it is running
- Boston Children's Hospital — Brookline, Massachusetts, United States
Full record on ClinicalTrials.gov
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