Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to determine if any improvements in depressive symptoms are maintained in the medium and longer-term (up to 3 months)


Clinical Trial Description

The duration of the study is 3 months Participants enrolled in the Almond Therapy group will have up to 9 in person visits, including the baseline visits, participants will receive Esketamine on 8 of these visits. There are 12 remote therapy sessions conducted via telephone or video, participants will also receive supportive text messages. In addition, participants will have 4 telephone calls from an independent assessor to ask questions about their mental health (MADRS). Participants enrolled in the Treatment as Usual group will have up to 9 in person visits, including the baseline visits, participants will receive Esketamine on 8 of these visits. Participants will continue to receive the therapy their treating physician felt was appropriate at the time of enrolment in the study. In addition, participants will have 4 telephone calls from an independent assessor to ask questions about their mental health (MADRS). Participants will receive intranasal Esketamine 56mg or 84 mg once weekly for 4 weeks and 56 mg or 84 mg once every 2 weeks for 8 weeks as per Product Monograph ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05438758
Study type Interventional
Source Zylorion Health
Contact
Status Withdrawn
Phase Phase 2
Start date January 15, 2023
Completion date March 1, 2024

See also
  Status Clinical Trial Phase
Terminated NCT05323019 - Repeated Intranasal Esketamine Plus Almond Therapy in Patients With Treatment Resistant Depression Phase 2
Completed NCT02977299 - Comparative Effectiveness Research Trial for Antidepressant Incomplete and Non-responders With TRD Phase 4
Completed NCT02741791 - A Study to Assess the Efficacy and Safety of AXS-05 in Subjects With Treatment Resistant Major Depressive Disorder Phase 3
Terminated NCT03254017 - Remotely Programmed Deep Brain Stimulation of the Bilateral Habenula for Treatment- Resistant Major Depression: An Open Label Pilot Trial N/A
Active, not recruiting NCT01798407 - DBS of the Lateral Habenula in Treatment-Resistant Depression N/A
Completed NCT00986479 - This is a Study to Determine the Antidepressant Effects of AZD6765 Phase 2