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Prehospital Study at the Universitair Ziekenhuis Brussel II

NCT02270541 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 140

Last updated 2016-03-02

No results posted yet for this study

Summary

Interventional prospective randomized open blinded end-point (PROBE) single-center clinical trial on the evaluation of the efficacy, safety, feasibility, reliability, and cost-effectiveness of in-ambulance telemedicine for patients with suspicion of acute stroke.

Conditions

Interventions

OTHER

Telemedicine

In-ambulance telemedicine

Sponsors & Collaborators

  • Research Foundation Flanders

    collaborator OTHER

  • Vrije Universiteit Brussel

    collaborator OTHER

  • Brussels Institute for Research and Innovation (INNOVIRIS)

    collaborator UNKNOWN

  • King Baudouin Foundation

    collaborator OTHER

  • Universitair Ziekenhuis Brussel

    lead OTHER

Principal Investigators

  • Jacques De Keyser, MD PhD · Universitair Ziekenhuis Brussel

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2016-02-29
Completion
2017-02-28

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Diseases

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 NCT02270541 on ClinicalTrials.gov