Overview

SSRIs vs. TCAs for Depression in ALS Patients

Status:
Completed
Trial end date:
2019-05-30
Target enrollment:
Participant gender:
Summary
Depression is seen in 9-11% of ALS patients and adequate and proper treatment is needed. In this study, ALS patients will be screened for depression using self-reported multiple choice questionnaire. Patients who fulfill the criteria for depression based on this screening tool will be evaluated by psychiatrist before inclusion in the study. The investigators will also measure quality of life and functional status by simple questionnaires. The patients will be allocated into two treatment groups to receive either TCA or SSRI for 12 weeks. Patients will be evaluated every 4 weeks and phone calls will be made in between the visits if needed to assess about efficacy and any side effects. If any patient reports having suicidal thoughts on any of these phone calls or clinic visits, he/she will be immediately sent to the ER for appropriate management. The investigators will repeat the questionnaires in the clinic visits, and use them in the data analysis to look for any improvement and to compare the two medication classes used in this study. This data may be used later on to do larger studies and help to make standard recommendations in treating depression in ALS patients.
Phase:
Early Phase 1
Details
Lead Sponsor:
St. Louis University
Treatments:
Antidepressive Agents
Antidepressive Agents, Tricyclic
Serotonin
Serotonin Uptake Inhibitors