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Clinical study of fire acupuncture therapy in patients with pain in Parkinson's disease

Clinical study of fire acupuncture therapy in patients with pain in Parkinson's disease

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084951
Enrollment
Unknown
Registered
2024-05-28
Start date
2022-01-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

parkinson disease

Interventions

Control group:Taking levodopa
Taking levodopa:fire acupuncture at DU16, GB20, BL10, GB12, Ashi point.

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The age ranged from 50 to 80 years; 2. The patients met the diagnostic criteria of Western and Chinese medicine for Parkinson's disease, as well as pain diagnostic criteria; 3. The patients met the characteristics consistent with chronic pain (the pain duration greater than 3 months); 4. The occurrence of pain was associated with the course of Parkinson's disease. The patients with a VAS score of 3 or more ;5.H-Y>4; 6. Currently effective dopaminergic drug therapy for Parkinson's disease in patients with no other treatment available ;7. No language and mental retardation (mini-mental State examination (MMSE)=22), can successfully complete the assessment related scales ;8. Patients who are willing and able to cooperate with treatment.

Exclusion criteria

Exclusion criteria: 1.The pain from other causes (e.g., inflammation, definite trauma, tumors, and other related conditions); Or those patients who with primary or secondary chronic pain unrelated to Parkinson's disease, and the pain is non-persistent; 2. The patients has had surgery related to bone and joints; 3.Patients who take more than 1.5g of levodopa per day are not effective in treatment or experience a significant decrease in effect and serious adverse effects due to drug reduction; 4.Patients with secondary Parkinson's syndrome or Parkinsonism-Plus syndrome; 5.H-Y=4; 6.The patient's Cranial MRI suggested a recent intracranial lesion; Patients with serious medical diseases such as heart, liver, kidney, hematopoietic system disorders or malignant tumors, and mental disorders; Patient's inability to take medication on time and cooperate with tests;7. Patients who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
King's Parkinson's Disease Pain Scale;

Secondary

MeasureTime frame
Visual analogue scale;Unified-Parkinson Disease Rating Scale;Parkinson’s Disease Questionnaire - 39;

Countries

China

Contacts

Public ContactChen Peng

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University

Chenpenger@126.com+86 138 1083 0776

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026