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Study on Effect of Warming the Kidney and Strengthening the Spleen Method on Intestinal Microbiota Imbalance and Cognitive Function in Parkinson's Patients

The Effects and Clinical Implications of Traditional Chinese Medicine Warming the Kidney and Strengthen the Spleen Method Combined with Conventional Treatment on Gut Microbiota Dysbiosis and Cognitive Function in Parkinson's Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000257
Enrollment
Unknown
Registered
2026-02-03
Start date
2023-10-18
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Parkinson's Disease

Interventions

study group: the study group treated with Domdesivir tablets on the basis of conventional treatment plus warming kidney and spleen strengthening formula
control group:treated with western medicine Domdesivir tablets

Sponsors

Jiangxi Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: (1) Meeting the above Western medicine diagnostic criteria for Parkinson's disease, and conforming to the traditional Chinese medicine diagnostic and pattern differentiation criteria for "tremor syndrome" (essential tremor) with spleen-kidney yang deficiency pattern; (2) Aged 50–80 years, regardless of gender; (3) All cases were assessed using the Hoehn–Yahr staging scale prior to inclusion, with stages 1–3 eligible; (4) All participants voluntarily joined the trial and provided signed informed consent forms prior to enrollment.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: (1) Patients who do not meet the above diagnostic and inclusion criteria; (2) Those with a Hoehn-Yahr stage = 4; (3) Patients whose traditional Chinese medicine pattern differentiation does not correspond to spleen-kidney yang deficiency pattern; (4) Patients with cognitive impairment or severe psychiatric disorders who are unable to cooperate with the completion of the clinical trial; (5) Patients accompanied by multiple organ failure; (6) Patients with allergic constitution; (7) Those who have participated in other clinical trials within the past 3 months or are currently participating in a similar trial.

Design outcomes

Primary

MeasureTime frame
UPDRS;

Secondary

MeasureTime frame
MoCA ;PDQ-39;gut microbiota;

Countries

China

Contacts

Public ContactYU Ting

Jiangxi Provincial People's Hospital

546617784@qq.com15083826658

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026