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Taking people in United StatesPhase 2

Ketamine added to usual pain medicine for sickle cell pain crises in young people

Tests low-dose ketamine with usual opioid pain medicine in young people with sickle cell disease.

Plain-language title generated from the registry record
Registry title: Sub-dissociative Dose Ketamine in Treatment of Vaso-occlusive Pain Event in Children and Young Adults

Key facts

Where
Torrance, United StatesSee the site
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 5 and 20 years old?

Source: NCT07369024, who can take part

Where in United States

  • Harbor-UCLA Medical CenterTorrance, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Mohsen Saidinejad
Trial code
NCT07369024
Record updated
2 September 2026
Original description
The purpose of this research is to see if ketamine is effective and safe in treating children and young adults with sickle cell disease experiencing sickle cell related pain. In this study, we will compare the outcomes (such as pain scores) in persons who receive standard of care pain medicine (an opioid such as morphine) plus a low dose (amount) of ketamine to those who receive only standard of care pain medicine.Read full original descriptionShow less

Sub-dissociative Dose Ketamine in Treatment of Vaso-occlusive Pain Event in Children and Young Adults: A Randomized Control Trial

The purpose of this research is to see if ketamine is effective and safe in treating children and young adults with sickle cell disease experiencing sickle cell related pain. In this study, we will compare the outcomes (such as pain scores) in persons who receive standard of care pain medicine (an opioid such as morphine) plus a low dose (amount) of ketamine to those who receive only standard of care pain medicine.

Inclusion: Between the ages 5-20 years; Diagnosed sickle cell disease. Homozygous (HbSS) or heterozygous (HbSC, HbSBetaThal Plus or Zero) will be included; Presenting with VOE pain, requiring IV pain medication; First dose of analgesic medication is given before patient approached for participation in the study; Primary language is English or Spanish; Adult individual or parent/legal guardian is able and willing to provide informed consent. For individuals 7 to 17 years of age, assent must also be provided when cognitively possible.

Exclusion: History of prior adverse reaction to ketamine; Patients with acute mania or history of bipolar disorder with manic episodes, history of hallucinations or paranoia secondary to previously diagnosed psychiatric condition; Pregnant or potentially pregnant patients per patient report. All patients of childbearing potential will undergo pregnancy testing prior to enrollment (as part of clinical care), and if positive, will be excluded; History of hypertension - Patients with active/uncontrolled hypertension defined as systolic 140 mmHg over diastolic of 90 mmHg will be excluded from participation in the study. If hypertension is controlled and at the time of enrollment, systolic and diastolic thresholds of 140 mmHg and 90 mmHg respectively are not exceeded, patient may be included in the study; History of significant or uncontrolled cardiovascular disease, liver disease, kidney disease, and thyroid disease; Elevated liver enzymes (alkaline phosphatase, ALT, AST, bilirubin) as sign of hepatic disfunction if the laboratory results are available prior to study participation; Sickle cell trait only; Patients whose primary language is other than English or Spanish; Pain attributed to causes other than VOE; Not requiring IV for pain treatment; No analgesic (e.g. opiate) is given before approach for study participation due to any reason, including problem with IV access; Oxygen saturation < 90% on room air; Patients with evidence of increased intracranial pressure; Patients with elevated intraocular pressure; Patients who appear intoxicated on any substance; Patients who are wards of the state or prisoners as defined by DHS; Patients who are not deemed to be competent to provide consent or assent.

ClinicalTrials.gov NCT07369024