Profile of genetic mutation and variation in early-onset Parkinsonâ€™s disease patient in Thailand

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

TCTR

Registry ID

TCTR20180316002

Enrollment

Registered

2018-03-16

Start date

2018-03-22

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Genetic mutation in early&#45

Interventions

The group consists of patients with a diagnosis of clinically&#45

established or clinically&#45

probable Parkinson&#39

s disease who have onset of motor symptom during 20&#45

50 years old

Basic Science

Early&#45

onset Parkinson&#39

s disease

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: early-onset Parkinson's disease patient in King Chulalongkorn Memorial Hospital

Exclusion criteria

Exclusion criteria: patient who has parkinsonism caused by one of the following conditions: - traumatic brain injury - vascular parkinsonism - brain tumor - encephalitis - drug-induced parkinsonism

Design outcomes

Primary

Measure	Time frame
Genetic mutation Cross-section within study period Next generation base sequencing	—

Secondary

Measure	Time frame
Clinical manifestation of genetic PD Cross-section within study period Questionaire	—

Countries

Thailand

Contacts

Public ContactSekh Thanprasertsuk

Chulalongkorn University

sekh_ac120@hotmail.com022564267

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026

Profile of genetic mutation and variation in early&#45;onset Parkinsonâ€™s disease patient in Thailand