Text Size

uPHI: Wireless Body Area Network Core Technology

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2010 by Taipei Medical University WanFang Hospital.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Taipei Medical University WanFang Hospital
ClinicalTrials.gov Identifier:
NCT01200667
First received: September 10, 2010
Last updated: September 14, 2010
Last verified: September 2010
History of Changes
  Purpose

The application scenario is shown in the figure below: the user utilizes an ECG-based wireless sensor (WiBoC Chipset), and transmit those signals to a mobile-phone device that has an embedded expert system integrated. With the aid of 3G system, a remote healthcare monitoring center receives those uploaded signals and stores into the application server. According to the events from this server, the people on service responses to the emergency and takes the corresponding process.


Condition
Asystole
Sinus Bradycardia
Sinus Tachycardia
Sinus Arrhythmia
Atril Fibrillation

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: uPHI: Wireless Body Area Network Core Technology

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Taipei Medical University WanFang Hospital:

Estimated Enrollment: 380
Study Start Date: July 2010
Estimated Study Completion Date: September 2010
Estimated Primary Completion Date: September 2010 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   20 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
  • Emergency patient with chest pain.
  • Emergency patients were implementation of 12-lead EKG during observation.
  • Out-patient services of Cardiology with arrhythmia.
  • Adults over 20 years old.
Criteria

Inclusion Criteria:

  • Emergency patient with chest pain.
  • Emergency patients were implementation of 12-lead EKG during observation.
  • Out-patient services of Cardiology with arrhythmia history.
  • Adults over 20 years old.

Exclusion Criteria:

  • The patient required the intervention of resuscitation and cardiac massage.
  • Chest trauma
  • On pacemaker
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01200667

Locations
Taiwan
Taipei Medical University Wan Fang Hospital
Taipei, Taiwan
Sponsors and Collaborators
Taipei Medical University WanFang Hospital
Investigators
Principal Investigator: Ray-Jade Chen Taipei Medical University WanFang Hospital
  More Information

No publications provided

Responsible Party: Ray-Jade Chen/ Deputy Superintendent, Taipei Medical University Wan Fang Hospital
ClinicalTrials.gov Identifier: NCT01200667     History of Changes
Other Study ID Numbers: 0990004864
Study First Received: September 10, 2010
Last Updated: September 14, 2010
Health Authority: Taiwan: Department of Health

Additional relevant MeSH terms:
Arrhythmias, Cardiac
Arrhythmia, Sinus
Heart Arrest
Tachycardia
Tachycardia, Sinus
Sick Sinus Syndrome
 Bradycardia
Heart Diseases
Cardiovascular Diseases
Pathologic Processes
Tachycardia, Supraventricular
Heart Block

ClinicalTrials.gov processed this record on May 23, 2013