NCT07450430Not yet recruitingPhase 3
Optimal Timing of Ketamine Initiation for SCD Pain
Double-blind, Randomized, Placebo Controlled Study to Evaluate Optimal Timing of Ketamine Initiation
Source: ClinicalTrials.gov · Last updated 9 Mar 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- First submitted
- 13 Jan 2026
- Start date
- Feb 2026
- Primary completion date
- Feb 2029
- Lead sponsor
- Boston Children's Hospital
- Diseases
- Sickle cell disease
- NCT number
- NCT07450430
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 90
- From Feb 2026 to the primary completion date, Feb 2029
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- allergy to ketamine
Other
- severe side effects associated with ketamine
- unable to consent
Who the study is looking for
- sickle cell disease diagnosis
- presenting with pain to ED or infusion clinic
- patient at study site
- 6 to 24 years old
Age in the registry: 6 years to 24 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Boston Children's Hospital Coordinator of this site? Confirm its status | Brookline | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.