Viewing Study NCT05932550


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Study NCT ID: NCT05932550
Status: COMPLETED
Last Update Posted: 2023-07-06
First Post: 2023-06-28
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Safety of Maraviroc for Post-stroke Depression
Sponsor: Tel-Aviv Sourasky Medical Center
Organization:

Study Overview

Official Title: Safety of Maraviroc for Post-stroke Depression (Proof-of-concept)
Status: COMPLETED
Status Verified Date: 2023-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MRV-PSD
Brief Summary: Post-stroke depression (PSD) is a barrier to effective rehabilitation and recovery after stroke. Current treatment options are limited and there is an unmet need for specific and effective therapeutic options.

Objective: To examine the safety and efficacy of Maraviroc, a CCR5 antagonist, as a possible add-on treatment option for PSD, in an open-labeled proof-of-concept clinical trial.

Design, Setting, and Participants: A 10-week trial of daily oral 300 mg Maraviroc in ten patients with subcortical stroke suffering from PSD. Follow-up: eight weeks after completing treatment.

Main Outcome Measure: A change in the Montgomery-Asberg Depression Rating Scale (MADRS).
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: