Johns Hopkins University
Baltimore, Maryland, 21287, United States
NCT Number: NCT05378100
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.
This study is active but is not currently recruiting participants.
18 year–65 year
All sexes
Interventional
Phase 2
Baltimore, Maryland, 21287, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Infusion of ketamine 0.5 mg/kg over 40 minutes
Infusion of midazolam 0.05 mg/kg over 40 minutes
Time frame: Baseline (infusion visit) through four weeks after the infusion.
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.
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.
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.
The total score of the BDI-IIranges from 0 to 63. Higher scores denote more severe depression.
Johns Hopkins University
Other
Low-Dose Ketamine Infusion for the Treatment of Multiple Sclerosis Fatigue (INKLING-MS)
Acronym: INKLING-MS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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