OsciPulse D-dimer Efficacy Trial

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of the OsciPulse System in reducing serum d-dimer levels in hospitalized ischemic stroke patients.

Clinical Trial Description

After being informed about the study and potential risks, all patients giving written informed consent will be screened for eligibility. Eligible and enrolled patients who have been admitted to the hospital for an ischemic stroke will be randomized in a non-blinded study to receive compression therapy from either standard-of-care intermittent compression garments, or the OsciPulse System. During the duration of the subject's hospital stay serum d-dimer levels will be monitored serially. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05389488
Study type	Interventional
Source	OsciFlex LLC
Contact
Status	Withdrawn
Phase	Phase 2
Start date	December 2022
Completion date	March 2023

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