A Phase 2 interventional study of Ketamine and Midazolam in Multiple Sclerosis Fatigue, sponsored by Johns Hopkins University. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-05-28.
Sponsored by Johns Hopkins University · Phase 2, Interventional, and Treatment
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.
Johns Hopkins University is the lead sponsor of 1,783 studies on the registry; 313 are open to participants now.
Of its 203 completed or terminated interventional studies of FDA-regulated products, 140 (69%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Participants in this arm will receive two infusions of ketamine four weeks apart.
Drug: Ketamine
Participants in this arm will receive one infusion of ketamine followed four weeks later by an infusion of midazolam.
Drug: Ketamine · Drug: Midazolam
Participants in this arm will receive one infusion of midazolam followed four weeks later by an infusion of ketamine.
Drug: Ketamine · Drug: Midazolam
Infusion of ketamine 0.5 mg/kg over 40 minutes
Infusion of midazolam 0.05 mg/kg over 40 minutes
Modified Fatigue Impact Scale (MFIS) Score
The total score of the MFIS ranges from 0 to 84. Higher scores denote more severe fatigue.
Time frame: Baseline (infusion visit) through four weeks after the infusion.
Fatigue Severity Scale (FSS)
The total score of the FSS ranges from 1 to 7. Higher scores denote more severe fatigue.
Time frame: Baseline (infusion visit) through four weeks after the infusion.
Epworth Sleepiness Scale (ESS)
The total score of the ESS ranges from 0 to 24. Higher scores denote more severe sleepiness.
Time frame: Baseline (infusion visit) through four weeks after the infusion.
Beck Depression Inventory-II (BDI-II)
The total score of the BDI-IIranges from 0 to 63. Higher scores denote more severe depression.
Time frame: Baseline (infusion visit) through four weeks after the infusion.
Plan to share: Yes — After completion of the study and publication of key findings, the study investigators will make Final Research Data available to researchers upon written request. Researchers must adhere to a data sharing agreement. This agreement requires users to: (1) use the data only for research purposes; (2) not share the data with unauthorized users; (3) ensure that the data are protected from unauthorized persons; (4) require that the data be returned or destroyed at the end of the analysis; (5) provide certification of IRB review and approval.
Supporting information: Study protocol, Sap
No publications or documents are linked to this record.
This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.
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Johns Hopkins University