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PrescriptionNCT01668810

The Third Survey of Prescription Pattern of Psychotropic Drugs in China

An observational study of Prescription, run by Peking University at 1 site in China.

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 The sponsor has not verified this record for over two years, so it may be out of date.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 investigators aimed to examine the psychotropic prescription pattern in China. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Prescription
How many people
7,000 participants
Where
1 siteChina
Study dates
Jul 2012to Jul 2013
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 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: schizophrenia, depression and bipolar disorder patients

Who may be able to join

None listed.

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Yun-Ai Su, Phd. contact

8610-82801960

suyunai@gmail.com

China1 site, 1 recruiting
  • Institute of mental health, Peking University

    Beijing, Beijing Municipality, 100191

    Tianmei Si, PhD., 8610-82801960, si.tian-mei@163.com

    Tianmei Si, PhD.

    Recruiting

Other trials in China

About this study

Official title: The Third Survey on China Psychotropic Prescription for Schizophrenia, Depression and Bipolar Disorder

The investigators aimed to examine the psychotropic prescription pattern in China.

Conditions
Prescription
Keywords
prescription, schizophrenia, depression, bipolar disorder
Medical subject headings
Schizophrenia, Depression, Bipolar Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01668810
Study groupRoleWhat they receive
Beijing regioninclude six hospitals
Guangdong Provinceinclude 3 hospitals
Jiangsu provinceinclude 3 hospitals
Hebei provinceinclude 6 hospitals
Hubei Provinceinclude 7 hospitals
Shanxi provinceinclude 3 hospitals
Jiangxi provinceinclude 3 hospitals
Jilin provinceinclude 6 hospitals
Sichuan provinceinclude 3 hospitals
Shaanxi provinceinclude 3 hospitals

Timeline

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

  1. First posted20 Aug 2012 (estimated)
  2. Study startJul 2012
  3. Primary completionSep 2012 (estimated)
  4. Study completionJul 2013 (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
Ecologic or community
Time perspective
Prospective
Enrolment
7,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01668810
Sponsor's protocol ID
RISSCH4255
Status last verified
Jul 2012
First submitted
16 Aug 2012
Last updated
20 Aug 2012
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Prescription, run by Peking University at 1 site in China.

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 0 inclusion and 1 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 20 Aug 2012. 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 China. 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 Yun-Ai Su, Phd. (8610-82801960, suyunai@gmail.com), 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 20 Aug 2012.

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