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Physician's RoleNCT01267890

The Conflicts of Ethics and Law on Patient's Surrogate

An observational study of Physician's Role, run by China Medical University 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 The sponsor has not verified this record for over two years, so it may be out of date.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

This study is a prospective cross-sectional survey study. The investigators developed self-administrated questionnaire and recruit 120 physicians in two hospitals and 60 lawyers from some law firms to this study. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Physician's Role
How many people
120 participants
Where
1 siteTaiwan
Study dates
Dec 2010to Jul 2011
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 Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: 120 physicians in two hospitals

Who may be able to join

  • resident
  • visiting Staff
  • chief resident

Who cannot join

  • intern
  • clerk

Trial locations and contacts

1 site in 1 country.

Chih-Jaan Tai, Associate Professor contact

04-22053366 ext. 6321

cjtai@mail.cmu.edu.tw

Taiwan1 site, 1 recruiting
  • China Medical University Hospital

    Taichung, 40402

    Chih-Jaan Tai, Associate Professor, 04-22053366 ext. 6321, cjtai@mail.cmu.edu.tw

    Recruiting

Other trials in Taiwan

About this study

Official title: Health Service Administration China Medical University (Chih-Jaan Tai)

This study is a prospective cross-sectional survey study. The investigators developed self-administrated questionnaire and recruit 120 physicians in two hospitals and 60 lawyers from some law firms to this study.

To realize and compare the opinions of physicians and lawyers about controversial decision-making of surrogate.

Read the detailed description

This study provides three real scenarios regarding dilemma between ethics and law when patient's surrogate may not represent patient's best interest:1. Parents ask physician resect their mentally handicapped daughter's uterus. 2. A son refuse physician's suggestion of surgical treatment for his mother, instead, wishes donating his mother's kidney to his son. 3. A mother decides to give up treatment for her son's head injury because of his rebel behavior before.

T-test, ANOVA and Logistic Regression will be used to analyze in this study.

Keywords
ethics, law, surrogate, conflict

Timeline

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

  1. First posted29 Dec 2010 (estimated)
  2. Study startDec 2010
  3. Primary completionMay 2011 (estimated)
  4. Study completionJul 2011 (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
Case only
Time perspective
Cross-sectional
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01267890
Sponsor's protocol ID
CMU-DMR99-IRB-254
Status last verified
Dec 2010
First submitted
28 Dec 2010
Last updated
29 Dec 2010
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Physician's Role, run by China Medical University 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 3 inclusion and 2 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 29 Dec 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?

Contact Chih-Jaan Tai, Associate Professor (04-22053366 ext. 6321, cjtai@mail.cmu.edu.tw), or a site near the patient. 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 29 Dec 2010.

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