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OsciPulse D-dimer Pilot Trial

NCT06477016 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-03-30

No results posted yet for this study

Summary

Pilot, randomized, non-blinded clinical trial to generate preliminary data to evaluate the impact of the OsciPulse system on serum d-dimer levels compared to standard of care intermittent compression therapy for DVT prophylaxis in patients admitted in the neuro ICU or intermediate neurological care unit with acute ischemic stroke.

Conditions

Interventions

DEVICE

OsciPulse

Non-invasive device that provides rapid pulses of compression of the calves to modify venous blood flow patterns in immobilized persons.

DEVICE

Intermittent Pneumatic Compression

Non-invasive device that provides rapid pulses of compression of the calves to modify venous blood flow patterns in immobilized persons.

Sponsors & Collaborators

Principal Investigators

  • Steven Messe, MD · University of Pennsylvania

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-12
Primary Completion
2027-02-28
Completion
2027-02-28
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06477016 on ClinicalTrials.gov