Parkinson's Trial NCT03523104
Link gene changes to symptoms
- Trial ID
- NCT03523104
- Official Title
- The Chinese Parkinson's Disease With LRRK2 Variants Registry
- Goal
- Link gene changes to symptoms
- Status
- RECRUITING
- Sponsor
- Xiangya Hospital of Central South University
- Study Type
- OBSERVATIONAL
- Enrollment
- 1000 participants
- Conditions
- Parkinson Disease
Summary For Families
The goal is to build a database of people in mainland China with Parkinson's disease who carry changes in a gene called LRRK2, since certain LRRK2 changes are a common known genetic cause or affect the risk of Parkinson's. Participants give a blood sample to confirm the LRRK2 change, then researchers record symptoms and function using many standard rating scales such as the Unified Parkinson's Disease Rating Scale and other neurological tests, and they will also test blood markers like uric acid and signs of inflammation. The study is open to people diagnosed with Parkinson's by standard clinical criteria who test positive for an LRRK2 variant, and it aims to enroll about 1,000 participants in mainland China.
Locations
- Xiangya Hospital of Central South University, Changsha, Hunan, China
Frequently Asked Questions
- What is this trial testing?
- This trial is studying an experimental treatment. The goal is to build a database of people in mainland China with Parkinson's disease who carry changes in a gene called LRRK2, since certain LRRK2 changes are a common known genetic cause or affect the risk of Parkinson's. Participants give a blood sample to confirm the LRRK2 change, then researchers record symptoms and function using many standard rating scales such as the Unified Parkinson's Disease Rating Scale and other neurological tests, and they will also test blood markers like uric acid and signs of inflammation. The study is open to people diagnosed with Parkinson's by standard clinical criteria who test positive for an LRRK2 variant, and it aims to enroll about 1,000 participants in mainland China.
- Who can participate?
- Eligibility criteria vary. Check the full listing on ClinicalTrials.gov for detailed inclusion and exclusion criteria.
- Where is this trial located?
- This trial is recruiting at 1 location.
- Does it cost anything to join?
- You are never charged a fee to join a legitimate clinical trial, and the study treatment and study-specific tests are provided by the trial sponsor at no charge. In the US, routine care you would receive anyway can still be billed to you or your insurance; coverage rules differ by country, and trials in the UK and Canada usually run through public health systems. Travel, parking, and time are real costs, and some trials reimburse them while others do not. Before enrolling, ask the study coordinator to explain in writing what is and is not covered.
- How long does the trial last?
- This trial is estimated to last approximately 10 years.
- Can I leave the trial if I change my mind?
- Yes. You can withdraw from any clinical trial at any time, for any reason, without affecting your standard medical care. Trials are voluntary by law. The team may ask if you are willing to do a brief exit visit so they can collect safety information, but you are not obligated.
- Can my spouse or care partner come with me to visits?
- In most cases yes, and it is often encouraged. Care partners can help with notes, questions, and getting home safely after a long visit. Some study assessments do need to happen one on one, but care partners are usually welcome for the rest of the appointment.
- Will I get a placebo in this trial?
- This is an observational study, so there is no placebo and no experimental treatment is assigned. Researchers observe and collect information while you continue your usual care.
- What procedures are involved in this trial?
- Based on the protocol, this trial involves: Questionnaires & surveys (non-invasive). Confirm the full schedule with the study coordinator.