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临床试验/NCT05779475
NCT05779475Enrolling By Invitation不适用

An Observational Study of Patients With Moderate Parkinson's Disease

Novo Nordisk A/S8 个研究点 分布在 4 个国家目标入组 96 人开始时间: 2023年4月5日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
96
试验地点
8
主要终点
Change in Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III (motor score) in OFF state

研究概览

简要总结

The main purpose of this study is to follow and observe a group of people living with Parkinson's disease to see how study participation affects their signs and symptoms in the months after starting in the study. While taking part in this study participants will take their usual medication as prescribed. However, the study doctor may recommend adjustments to their medication to provide a better treatment of their Parkinson's disease. Participation will last from 3 up to 24 months. During visits to the clinic, the study doctor or study nurse will evaluate signs and symptoms of Parkinson's disease using several different assessments. At a minimum of 2 visits participants will be asked to undergo 'off'-assessments.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
50 Years 至 68 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female, aged 50-68 years (both inclusive) at the time of signing informed consent.
  • Diagnosed with Parkinson's disease using the Movement Disorder Society (MDS) criteria (fulfilling the definition of clinically probable Parkinson's disease).
  • Moderate Parkinson's disease, e.g. as defined by i) modified Hoehn and Yahr stage 2-3 in OFF state and ii) MDS-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III total score greater than or equal to (≥) 30 in OFF state, both as judged by the investigator.
  • Patient has symptoms that are not adequately controlled by existing oral anti-Parkinson's disease medications, i.e., having both ON and OFF periods, as judged by the investigator.
  • Parkinson's disease duration greater than (>) 5 years and lesser than or equal to (≤) 12 years from diagnosis at the time of signing informed consent.
  • Potential candidate for a future cell therapy transplantation, as judged by the investigator.
  • Life expectancy >7 years as judged by the investigator.

排除标准

  • Any atypical or secondary Parkinson's disease, or non-Parkinson's disease-suspected cause(s) of, or contributors to, parkinsonism, as judged by the investigator.
  • Significant drug-induced dyskinesias as judged by the investigator, e.g., as defined by a score of > 2 in the Abnormal Involuntary Movement Scale (AIMS), in any body part in the ON state.
  • Tremor-dominant Parkinson's disease, as judged by the investigator.
  • Cognitive impairment predictive of dementia (including Parkinson's disease dementia) or other cognitive dysfunction as judged by the investigator, e.g., as defined by Montreal Cognitive Assessment (MoCA) score ≤ 24, or evidence of major neurocognitive disorder according to the Diagnostic and Statistical Manual of Mental Disorders V (DSM-V) criteria.
  • Major medical or psychiatric disorder (e.g., depression (Montgomery-Asberg Depression Rating Scale (MADRS) >20) or psychosis), or other disease making the patient unsuited for participation in the study, as judged by the investigator.
  • Treatment for dystonia or spasticity within 3 months of screening (Botox for a focal dystonia is allowed).
  • Substantial neurological symptoms not accounted for by Parkinson's disease, including active seizure disorder, as judged by the investigator.

结局指标

主要结局

Change in Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III (motor score) in OFF state

时间窗: From baseline (week 0) to end of study (13 to 104 weeks from baseline)

Measured as score. MDS-UPDRS consists of 4 parts - has 65 items/questions in total. Part III assesses the motor function of the patient at the time of the visit conducted in both the OFF and ON state. Each item will receive a score ranging from 0 to 4, where 0 represents the absence of impairment and 4 represents the highest degree of impairment.

次要结局

  • Is the patient interested in being considered for participation in a cell therapy transplantation study (yes/no)(At end of study (13 to 104 weeks from baseline))
  • Change in MDS-UPDRS Part III (motor score) in OFF state(From last medication adjustment (between week 0 and week 104) to end of study (13 to 104 weeks from baseline))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (8)

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