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Telemedicine's Utility for Augmenting Clinical Trials and Informed Consent TACTIC

Withdrawn
Conditions
Stroke
Registration Number
NCT00390286
Lead Sponsor
University of California, San Diego
Brief Summary

This is a 6 year, Phase I, Clinical Research Protocol to study the feasibility of using a telemedicine system for performing research in a remote hospital system.

Detailed Description

The UCSD Telemedicine system is a digital video camera system, which can transfer video and audio images from a clinic or emergency room to a remote place where a physician can review images in real time (as they happen). The system uses site independent software to access the camera system from multiple locations. This research study will determine if it is feasible to obtain informed consent for various types of research trials (hypothetical, non-invasive, invasive trails) via telemedicine. Inpatient assessments on participants to complete clinical research case report forms by telemedicine will also by performed.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Male/Female, age 18 years or older
  • Clinical neurological focal deficits consistent with stroke
  • Time of onset 3-24 hours and with stable neurological deficit
  • Signed Informed Consent
Exclusion Criteria
  • Deficits known to be due to non-stroke etiology
  • Time of onset less than 3 hours
  • Patients unable to give consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of trials participant is enrolled into5 years

Counting how many patients are enrolled into OTHER clinical trials using a telemedicine technique

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UCSD Stroke Center

🇺🇸

San Diego, California, United States

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