The Third Survey of Prescription Pattern of Psychotropic Drugs in China

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT05045235` - Optimization of Drug Prescriptions in the Care Pathway for the Elderly, With the Final Objective of Reducing the Iatrogenic Risk
	Completed	`NCT04919889` - Implementation and Effectiveness of a Community-based Exercise on Prescription Program for Adults With Chronic Diseases
	Active, not recruiting	`NCT06212895` - Expectations of Patients Regarding Exercise in an Outpatient Clinic

See also

Status

Clinical Trial

Phase

Recruiting

NCT05045235 - Optimization of Drug Prescriptions in the Care Pathway for the Elderly, With the Final Objective of Reducing the Iatrogenic Risk

Completed

NCT04919889 - Implementation and Effectiveness of a Community-based Exercise on Prescription Program for Adults With Chronic Diseases

Active, not recruiting

NCT06212895 - Expectations of Patients Regarding Exercise in an Outpatient Clinic

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01668810
Study type	Observational
Source	Peking University
Contact	Yun-Ai Su, Phd.
Phone	8610-82801960
Email	suyunai@gmail.com
Status	Recruiting
Phase	N/A
Start date	July 2012
Completion date	July 2013

The Third Survey of Prescription Pattern of Psychotropic Drugs in China

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms