Skip to content

Exploring the molecular mechanism of DKK1-induced Parkinson's disease through inhibition of the Wnt/ß-catenin signalling pathway based on arginine methylation modification

Exploring the molecular mechanism of DKK1-induced Parkinson's disease through inhibition of the Wnt/ß-catenin signalling pathway based on arginine methylation modification

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127386
Enrollment
Unknown
Registered
2026-06-30
Start date
2025-02-02
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Parkinson's disease

Interventions

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 75 years old, gender not limited; 2. Diagnosed with primary Parkinson's disease; 3. The efficacy of the drug has significantly declined, or obvious motor complications have occurred, affecting the patient's quality of life. Or intolerable adverse drug reactions occur, affecting the efficacy of the drug; 4. There is stiffness or tremor that cannot be fully controlled by medication; 5. The Hoehn-Yahr stage was at least 2.5 stages; 6. Voluntarily participate in clinical trials and be able to sign informed consent forms;

Exclusion criteria

Exclusion criteria: 1. I have received surgical damage treatment before; 2. Pregnant women, lactating women, women of childbearing age who plan to conceive or have no safe contraceptive measures; 3. Drug users and alcoholics; 4. Obvious cognitive impairment (MMSE <= 17 points for primary school students and <= 24 points for middle school students and above); 5. There is severe depression or other serious mental illness that cannot be treated; 6. Those with a history of craniocerebral injury, tumors, or severe cerebrovascular diseases; 7. Severe brain atrophy (confirmed by CT or MRI); 8. The implanted site needs to undergo hyperthermia therapy; 9. Abnormal blood routine and blood biochemical tests, coagulation dysfunction, and severe abnormalities in liver and kidney functions; 10. Uncontrollable hypertension, severe heart disease or serious internal or respiratory diseases; 11. Long-term use of immunosuppressants or hormone therapy is required; 12. There are other concomitant diseases, and a pacemaker, defibrillator, cochlear implant or other nerve stimulator needs to be implanted or has been implanted; 13. Due to other types of diseases, repeated MRI examinations are required; 14. Those who have participated in any other clinical trials within three months before the operation; 15. Unwilling or unable to cooperate with the human implantation surgery of deep brain stimulation system components; 16. Unwilling or unable to cooperate with postoperative follow-up; 17. Those that researchers consider unsuitable;

Design outcomes

Primary

MeasureTime frame
Dopamine, TNF-a, IL-6, a -synuclein;Inflammation level;Inflammation level;

Countries

China

Contacts

Public ContactGeng Xin

First Affiliated Hospital of Kunming Medical University

gengxin@ydyy.cn+86 871 65324888

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026