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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
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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Boston Children's Hospital
Coordinator of this site? Confirm its status
BrooklineUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.