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Efficacy and mechanisms of acupuncture for pain in Parkinson's disease

Efficacy and mechanisms of acupuncture for pain in Parkinson's disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000325
Enrollment
Unknown
Registered
2026-02-09
Start date
2026-04-01
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

Acupuncture Group:In addition to the baseline treatment, patients received acupuncture at the following acupoints: Sishenzhen (EX-HN1), Shenting (GV24), Yintang (EX-HN3), bilateral Shenmen (HT7), bila
Sham Acupuncture Group:In addition to the baseline treatment, patients received sham acupuncture at the same set of acupoints as the acupuncture group. Treatment was administered once per day on Monda

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged 45–80 years, both males and females are eligible. (2) Hoehn–Yahr stage 1–3. (3) Have been on anti-PD medication for at least six months, with a stable dose maintained for at least one month prior to enrollment. (4) Able to understand and voluntarily sign the informed consent form. (5) Meet the diagnostic criteria for PD with pain. (6) Visual Analog Scale (VAS) score between 1 and 6, indicating mild-to-moderate pain.

Exclusion criteria

Exclusion criteria: (1) Patients with severe cognitive impairment and hallucinations who are unable to cooperate with scale assessments. (2) Patients with severe comorbidities, including senile psychosis, epilepsy, malignant tumors, endocrine and metabolic diseases, or severe cardiac, pulmonary, hepatic, renal, or other organ-related diseases. (3) Participation in other clinical trials involving drugs, acupuncture, or other interventions within one month prior to enrollment in this study. (4) Inability to regularly take anti-PD medication due to adverse reactions or other reasons. (5) Patients who have previously undergone or plan to undergo deep brain stimulation therapy or rectal infusion of levodopa during the study period. (6) Female patients who are pregnant, breastfeeding, or planning to become pregnant in the near future. (7) Patients unable to cooperate with acupuncture treatment. (8) Patients requiring analgesic medications such as opioids or nonsteroidal anti-inflammatory drugs.

Design outcomes

Primary

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

Secondary

MeasureTime frame
PainDetect Questionnaire;Unified Parkinson's Disease Rating Scale;Parkinson's Disease Quality of Life Questionnaire - 39;Hamilton Depression Rating Scale;Somatosensory Evoked Potentials;Glial Fibrillary Acidic Protein;Tumor Necrosis Factor-a;S100 Calcium-Binding Protein B;

Countries

China

Contacts

Public ContactZhuanglixing

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

zhuanglixing@163.com13822287775

Outcome results

None listed

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