This pilot study will assess the safety and feasibility of intravenous (IV) ketamine in older adults with Treatment-Resistant Depression (TRD).
In addition, this study will develop and utilize innovative methodological approaches to demonstrate the feasibility of precision medicine and mobile health approaches in depression treatment.
Compound Ketamine
Country United States of America
Visit trial
Status
Completed
Results Published
Start date
22 October 2020
End date
15 March 2022
Chance of happening
100%
Phase
Phase IV
Design
Open
Type
Interventional
Generation
First
Participants
30
Sex
All
Age
65- 99
Therapy
No
Trial Details
Participants in this study will receive ketamine infusions twice a week for 4 weeks (acute phase). Participants who respond or remit will continue with an additional 4 weeks of weekly ketamine infusions (continuation phase). Participants will be assessed at baseline, end of acute phase, and end of continuation phase for effectiveness, safety, and executive functioning. Participants will be asked to complete daily surveys of their depression symptoms during their participation.NCT Number NCT04504175
Sponsors & Collaborators
Washington University School of MedicineLocated in St. Louis Missouri, researchers at the Washington University School of Medicine have conducted a number of studies with psychedelics inlcuding ketamine, psilocybin and nitrous oxide.