Skip to content

A Follow-up of the Influencing Factors of Dyskinesia in Patients With Parkinson's Disease

A Follow-up of the Influencing Factors of Dyskinesia in Patients With Parkinson's Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04453995
Acronym
PDDIFFU
Enrollment
300
Registered
2020-07-01
Start date
2019-01-05
Completion date
2022-06-01
Last updated
2020-07-01

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

Conditions

Dyskinesias, Parkinson Disease

Keywords

Parkinson disease, Dyskinesia, follow up

Brief summary

Parkinson' patients who have not had dyskinesia would be observed for 2 years in a multicenter prospective study with the purposes to clarify the predicting factors of dyskinesia.

Detailed description

Parkinson' patients with daily levodopa dosage above 200mg and no dyskinesia would be recruited into the study. They would be observed for two years for analyzed the predicting factors of dyskinesia. At the baseline, demographic information, Clinical information, blood sample, picture of tongure coating would be collected at the baseline. All participants were evaluated every three months for two years. The severity of motor symptoms were evaluated every 6 months.

Interventions

None listed

Sponsors

Shanghai Municipal Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University
CollaboratorOTHER
Second Affiliated Hospital of Soochow University
CollaboratorOTHER
The Affiliated BenQ Hospital of Nanjing Medical University
CollaboratorUNKNOWN
The Affiliated Hospital of Qingdao University
CollaboratorOTHER
The First Affiliated Hospital with Nanjing Medical University
CollaboratorOTHER
Zhejiang Provincial Tongde Hospital
CollaboratorOTHER
Shaoxing Hospital of Traditional Chinese medicine
CollaboratorUNKNOWN
The First People Hospital of Hangzhou Lin An District
CollaboratorUNKNOWN
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

\- 1) Patients have been clinically diagnosed with Parkinson disease at the recruitment. 2\) Patients have received Levodopa treatment with the daily dosage above 200mg.

Exclusion criteria

* 1\) be suspicious of atypical Parkinson or other Parkinson syndrome. 2) have experienced dyskinesia. 3) incorporation to the investigation

Design outcomes

Primary

MeasureTime frameDescription
the occurrence of dyskinesia and its related predicting factorsThe data would be analyzed within 9 months of the study completion. The outcome would be reported within 1 year of the the study completion.to evaluate the occurrence of dyskinesia during the 2 years of follow-up and identify its predicting factors of dyskinesia

Secondary

MeasureTime frameDescription
to evaluate patients ' living quality and the severity of non motor symptoms during the 2 years of follow-upThe data would be analyzed within 9 months of the study completion. The outcome would be reported within 1 year of the the study completion.to evaluate patients ' living quality and the severity of non motor symptoms during the 2 years of follow-up

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026