Not Yet RecruitingPhase 3ketamine

Optimal Timing of Ketamine Initiation for SCD Pain

Sponsored by Boston Children's Hospital

NCT ID
NCT07450430
Target Enrollment
90 participants
Start Date
2026-02
Est. Completion
2030-02

About This Study

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.

Conditions Studied

Sickle Cell DiseaseSickle Cell Crisis

Interventions

  • Ketamine hydrochloride injection
  • Placebo

Eligibility

Age:6 Years - 24 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* sickle cell disease diagnosis
* presenting with pain to ED or infusion clinic
* patient at study site
* 6 to 24 years old

Exclusion Criteria:

* allergy to ketamine
* severe side effects associated with ketamine
* unable to consent

Study Locations (1)

Boston Children's Hospital
Brookline, Massachusetts, United States

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source