Treatment of Parkinson Disease With Transplantation of SVF Cells of Adipose Origin: Safety and Exploratory Efficacy Study
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Incidence of treatment related adverse events
研究概览
简要总结
This is an interventional study to treat 10 patients with a diagnosis of Parkinson's disease with neurological assessment from the Oxford Parkinson's Disease Quotient-39 (PDQ-39) and Movement Disorders Society Universal Parkinson's Disease Rating Scale (MDS-UPDRS), with autologous adipose tissue-derived stromal vascular fraction (SVF) cells by subdermal plane injection into the submuscular aponeurotic fascia of the face.
This study assesses: 1) safety and 2) feasibility and 3) exploratory evidence of efficacy.
详细描述
Pre-procedure/intervention evaluation
Patients had a medical history, physical exam, and medication review. Neurological examination used two instruments: PDQ-39 and the MDS-UPDRS, the latter including videorecording of a standardized motor examination. Subjects also completed the general health questionnaire SF-36 and have blood drawn for subsequent biomarker analysis (immune markers L-1beta, IL-2, IL-6, IL-10, and TNF-alpha). Patients had pre-operative laboratory studies (hemogram, coagulation profile, electrolytes, BUN, creatinine, and urinalysis) and anesthesia evaluation carried out 48 hours prior to procedures.
Surgical and biochemical technique
The autologous fat tissue was harvested via liposuction by a plastic surgeon. The fat was washed and processed with collagenase for 60 minutes at a temperature of 39-41ºC, in an incubator and by constant shaking with a rotary shaker. The digested adipose tissue was then centrifuged for 14 minutes in 3 steps and the cell fraction (SVF) contained in the fat was removed with a syringe. The cell count was performed using a Luna Stem cell counter (Logos Bio). SVF was injected the same day as the liposuction and adipose processing.
A standardized total dose of 30x10e6 SVF cells was administered [Carstens 2017]. Injections of SVF cells bilateral (into the subdermal plane along the submuscular aponeurotic fascia) 1 cc per site for a final dose of 0.3 million cells per site
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects with UK brain bank criteria for idiopathic Parkinson's disease for a period of not less than one year
- •Age 18 - 80; male or female
- •Stable PD medication for at least 30 days prior to study enrollment
- •A MDS-UPDRS total score > 20 and < 50
- •Ability to understand the study and sign consent forms
- •Intent to comply with all postoperative appointments
- •Social support to be able to comply with all follow-up visits
排除标准
- •Previous neurological disease or previous brain trauma as a confounding factor
- •Cardiovascular disease or any condition that prohibits general anesthesia
- •Inability to understand and / or cooperate with investigators
- •Subjects that have a history of injury, infection, or deformity of at or near the anatomical site for planned product injection which may increase their risk for infection, injury, or complication related to the product (e.g., prior injury to blood vessels, lymphatics, history of orbital injury/fracture).
- •Rash or possible skin infection over surgical sites or face.
- •Subjects that use any form of tobacco, including e-cigarettes, more than once a week over the past year.
- •Current substance abuse (drugs or alcohol) within the 6 months prior to study enrollment
结局指标
主要结局
Incidence of treatment related adverse events
时间窗: 12-months follow-up post intervention.
Documentation of adverse events
L-dopa medication
时间窗: Up to month 12 post intervention.
Changes in L-dopa medication measured as levodopa-equivalent dose.
Minimal clinically important differences (MCIDs)-1
时间窗: Up to 12-months post SVF treatment
Estimation of MCIDs scores (0-199) based on the UPDRS scale: : MCID 4.3 points low, MCID 8.1 points medium, and MCID 17.1 points high.
Minimal clinically important differences (MCIDs)-2
时间窗: Up to 12-months post SVF treatment
Estimation of MCIDs scores (0-100) based on the PDQ-39 scale: : MCID 4.7 minimal, MCID 7.7 moderate, and MCID 10.1 significant.
次要结局
未报告次要终点
研究者
Samuel Vilchez, PhD
Professor
National Autonomous University of Nicaragua