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NCT05378100Active, not recruitingPhase 2

Ketamine for Multiple Sclerosis Fatigue

Low-Dose Ketamine Infusion for the Treatment of Multiple Sclerosis Fatigue (INKLING-MS)

Source: ClinicalTrials.gov · Last updated 28 May 2026

Brief summary (registry, in English)

The proposed study is a single-center, phase II, randomized, double-blind, parallel-group, active-placebo-controlled trial of intravenous low-dose ketamine in patients with MS fatigue.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
110 (estimated)
First submitted
12 May 2022
Start date
Jan 2023
Primary completion date
May 2026
Lead sponsor
Johns Hopkins University
NCT number
NCT05378100

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 110
  • From Jan 2023 to the primary completion date, May 2026
  • 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.

Prior treatment

  • History of prior ischemic or hemorrhagic stroke and cerebral vascular aneurysms.
  • Taking any disallowed therapy(ies), as noted in the protocol.

Other illness

  • Neurodegenerative disorders other than relapsing or progressive MS
  • History of coronary artery disease or congestive heart failure
  • Uncontrolled hypertension at Screening (history of high blood pressure and screening systolic blood pressure \>160 or diastolic blood pressure\>100)
  • History of severe liver disease, including cirrhosis
  • Terminal medical conditions
  • Currently treated for active malignancy
  • A history of intolerance or allergic or anaphylactic reaction to ketamine or midazolam
  • Clinically unstable medical or psychiatric disorders that require acute treatment as determined by the PI
  • History of severe or untreated coronary artery disease or history of congestive heart failure
  • History of recurrent seizures or epilepsy

Lab values

  • Having a known clear cause for secondary fatigue, such as untreated sleep apnea, untreated hypothyroidism, chronic liver disease, history of moderate to severe anemia (hemoglobin concentration of less than 9 gr/dl in men or less than 8 gr/dl in women).

Other

  • BDI-II score of more than 29 (indicating severe depression)
  • Breastfeeding or pregnant
  • Alcohol or substance abuse in the past year (except marijuana or other cannabinoids)

Who the study is looking for

  • Subject must be a man or woman, 18 to 65 years of age, inclusive.
  • Subject must be medically stable based on physical examination, medical history, and vital signs
  • Subject must meet McDonald 2017 diagnostic criteria for multiple sclerosis based on the PI review of the medical records
  • Subject must complain from fatigue as one of their main symptoms and have a screening MFIS score equal or higher than the cutoff based on gender, age, and education displayed in Table-226
  • Subject must be ambulatory (able to walk at least 20 feet using bilateral assistance)
  • Subject must have internet and email access and ability to use a computer or tablet or smartphone
  • Subjects that are currently taking medication for alleviating fatigue (such as amantadine, modafinil and armodafinil, and amphetamine-like psychostimulants) at Screening are eligible to participate unless the medication is one of the disallowed therapies (Table 3). Subjects taking a fatigue medication at the Screening visit must have been receiving a stable dose for at least four weeks before the Screening visit and be willing to continue the medication at the same dose for the duration of the study.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status

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