At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 34 enrolled
Drug / intervention
Fluoxetine 20 MG Oral Tabletdrug
Likely dose
Fluoxetine 20 MG Oral Tabletfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
MAMBO: Measuring Ambulation, Motor, and Behavioral Outcomes With Post-Stroke Fluoxetine in Tanzania
In Brief
A Phase 2 clinical trial evaluating Fluoxetine 20 MG Oral Tablet for Acute Stroke and Stroke, Ischemic. Completed, enrolled 34 participants across 1 site.
Detailed Summary
This is a phase II, randomized study of 120 adults age 18 or above who will prescribed 20mg daily Fluoxetine for 90 days following acute, ischemic stroke.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAcute Stroke, Stroke, Ischemic
CountriesTanzania
CollaboratorsMuhimbili University of Health and Allied Sciences
Timeline
Phase 2CompletedFinished
20192020202120222023202420252026
First PostedNov 2018
Enrollment StartNov 2019
Primary CompletionJan 2021
TodayJul 2026
First PostedNov 1, 2018
Enrollment StartNov 26, 2019
Primary CompletionJan 6, 2021
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 7.7 years ago
Interventions
Fluoxetine 20 MG Oral Tabletdrug
Once-daily dosing for 90 days