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AsystoleuPHINCT01200667

uPHI: Wireless Body Area Network Core Technology

An observational study of Asystole and Sinus Bradycardia, run by Taipei Medical University WanFang Hospital at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 20 years and olderHealthy volunteers can take part
Conditions the study is for
Asystole, Sinus Bradycardia, Sinus Tachycardia
How many people
380 participants
Where
1 siteTaiwan
Study dates
Jul 2010to Sep 2010
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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.

Who may be able to join

  • 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.

Who cannot join

  • The patient required the intervention of resuscitation and cardiac massage.
  • Chest trauma
  • On pacemaker

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Taipei Medical University Wan Fang Hospital

    Taipei

Other trials in Taiwan

About this study

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.

Medical subject headings
Heart Arrest, Tachycardia, Sinus, Arrhythmia, Sinus

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Sep 2010 (estimated)
  2. Study startJul 2010
  3. Primary completionSep 2010 (estimated)
  4. Study completionSep 2010 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
380 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01200667
Sponsor's protocol ID
0990004864
Acronym
uPHI
Status last verified
Sep 2010
First submitted
10 Sep 2010
Last updated
15 Sep 2010
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Asystole and Sinus Bradycardia, run by Taipei Medical University WanFang Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 15 Sep 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2010; AzTrials last refreshed its copy on 27 Oct 2026.

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