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临床试验/NCT00629161
NCT00629161Unknown2 期

Clinical Trial on the Effectiveness of Traditional Chinese Medicinal Mixture in Parkinson Disease

Fudan University10 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2008年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
144
试验地点
10
主要终点
Unified Parkinson's Disease Rating Scale (UPDRS)

研究概览

简要总结

This study was designed to evaluate the symptomatic effects or potential disease progression slowing down effect of a kind of Traditional Chinese Medicinal Mixture in Parkinson's disease (PD) patients. The treatment phase includes 12 months period of Traditional Chinese Medicinal Mixture per day or placebo and 1 month wash-out period without herbal medicine and placebo.

详细描述

The design of the study was a prospective, randomized, multicenter, double-blind placebo-controlled protocol. The intervention includes Traditional Chinese Medicinal Mixture tid or matched placebo.

Participating study centers include Neurological University Outpatient Clinics and Neurological Departments of Community-based Hospitals experienced with PD patients.

The primary outcome measure was the combined Unified Parkinson's Disease Rating Scale (UPDRS).

The hypothesis of this study was that Traditional Chinese Medicinal Mixture improves the overall wellbeing of PD patients and thus may leads to an improvement of parkinsonian symptoms in PD patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Parkinson's disease according to the UK Brain Bank criteria
  • Hoehn & Yahr stadium Ⅰ~Ⅲ
  • Age over 50 years
  • Taking only levodopa and/or dopamine agonists when recruiting
  • Consistent with the liver kidney deficiency type by Traditional Chinese Medicine (TCM) standard
  • Patients voluntarily take part in this study and signed the informed consent

排除标准

  • Modified Hoehn-Yahr scale are higher than 4
  • Had other serious illness such as liver/kidney failure, serious infection etc
  • Allergic to the study drug
  • Had been participated in other clinical trials during the last 3 months prior to study inclusion.
  • Taking Coenzyme Q10, MAO-B inhibitors, or vitamin E, all of which might improve the symptom or slowdown the progression of PD.
  • Taking herbal medicine that can nourish the liver and kidney by TCM standard.
  • Had serious mental disorder and could not describe his/her symptom.

研究组 & 干预措施

B

Placebo Comparator

干预措施: placebo (Drug)

A

Experimental

干预措施: Traditional Chinese Medicinal Mixture (composed of Roucongrong and adjuvant) (Drug)

结局指标

主要结局

Unified Parkinson's Disease Rating Scale (UPDRS)

时间窗: 13 months

次要结局

  • Dose of dopamine Agonists per day(13 months)
  • Parkinson disease sleep scale (PDSS)(13 months)
  • Hoehn & Yahr scale(13 months)
  • Schwab & England score(13 months)
  • The liver kidney deficiency scale score by Traditional Chinese Medicine standard(13 months)
  • Dose of levodopa per day(13 months)
  • Assessment of autonomic dysfunction in Parkinson disease (SCOPA-AUT)(13 months)
  • Changes in laboratory indexes as safety assessment, including red blood cell(RBC), white blood cell(WBC), platelet(PLT), alanine transaminase(ALT), aspartate transaminase (AST), blood urea nitrogen (BUN), creatinine(Cr) in blood samples, ect.(12 months)

研究者

申办方类型
Other

研究点 (10)

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