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Cohort Study of Tardive Dyskinesia in China

Cohort Study of Tardive Dyskinesia in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084119
Enrollment
Unknown
Registered
2024-05-10
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tardive dyskinesia

Interventions

none TD group:none

Sponsors

Peking University Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) At least 3 months of use of antidepressants, antipsychotics, calcium channel blockers and other drugs that may cause TD; 2) Moderate involuntary movement in at least one site (AIMS= 3 points) or mild involuntary movement in at least two sites (AIMS=2 points) ; 3) Sign the consent form voluntarily and be willing to cooperate with the study.

Exclusion criteria

Exclusion criteria: 1) Exclude other diseases that may cause involuntary movement, such as hereditary dystonia, Huntington's disease, chorea minor, etc.; 2) Those who are unable to complete genetic testing, imaging examination and scale assessment due to intellectual disability or serious physical disease.

Design outcomes

Primary

MeasureTime frame
Abnormal Involuntary Movement Scale, AIMS;

Countries

China

Contacts

Public ContactYuan Li

Peking University Sixth Hospital

ly141121@126.com+86 131 6750 7248

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026