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Clinical Trial Details

Trial ID: L0765
Source ID: NCT02407821
Associated Drug: Escitalopram
Title: The Routine Use of SSRI's at the Initiation of End-stage Renal Disease Treatment (RoSIE)
Acronym: RoSIE
Status: TERMINATED
Study Results: NO
Results:
Conditions: End Stage Renal Disease
Interventions: DRUG: Escitalopram|DRUG: Placebo
Outcome Measures: Primary: Proportion of consecutive incident dialysis patients that are eligible, 12 months|Proportion of eligible patients that will consent to randomization, 12 months|Proportion of randomized patients that comply with their group assignment, Compliance defined as \>80% of doses taken, 12 months | Secondary: Serious adverse events, 12 months|Number of patients withdrawn from the study drug due to QTc prolongation, 12 months|Completion rate for all secondary outcome measures (KDQoL, HUI-III, PHQ-9, Handgrip and 2-Minute Walk Test), 3 months and 6 months|Death, 12 months|Hospital-free days, 12 months
Sponsor/Collaborators: Sponsor: University Health Network, Toronto | Collaborators: McMaster University|Unity Health Toronto|University of Toronto
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 25
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2015-03
Completion Date: 2017-01
Results First Posted:
Last Update Posted: 2018-10-11
Locations: St. Joseph's Healthcare Hamilton, Hamilton, Ontario, L8N 4A6, Canada|St. Michael's Hospital, Toronto, Ontario, M5B 1W8, Canada|University Health Network, Toronto, Ontario, M6G 2K8, Canada
URL: https://clinicaltrials.gov/show/NCT02407821