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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04146519
Other study ID # 20171292
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date July 1, 2017
Est. completion date December 31, 2021

Study information

Verified date February 2021
Source Belarusian Medical Academy of Post-Graduate Education
Contact Vladimir Ponomarev, PhD
Phone 80172959016
Email professor.ponomarev@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Treatment of patients with Parkinson's disease using mesenchymal stem cells is a perspective method to influence on the pathogenesis of the disease. At the same time, this is a complex and still insufficiently explored process. Autologous mesenchymal stem cells will be transplanted to 30 patients with Parkinson's disease. The results of the effectiveness of the combined and intravenous routes of mesenchymal stem cells administration on the motor and non-motor symptoms in these patients will be evaluated and compared with the results of control group that received placebo therapy


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 31, 2021
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 69 Years
Eligibility Inclusion Criteria: 1. A reliable diagnosis of Parkinson's disease, according to the diagnostic criteria developed by the Brain Bank of the Society for Parkinson's disease of Great Britain (UK Brain Bank Criteria, 1992). 2. Stage of the disease according to Hen-Yar: 1.5 - 3.0 stage. 3. Rapidly progressive type with a change in the stages of Parkinson's disease in no more than 4 years. 4. A good response to levodopa treatment: a positive dopamine test for assessing motor functions by a total score of section 3 of the UPDRS scale in the on- and off-period (not less than 30%). 5. The duration of the disease is not more than 8 years with the absence of motor fluctuations and dyskinesias. 6. The age of patients is up to 65 years Exclusion Criteria: e and parkinsonism-plus. 2. Severe concomitant diseases (congestive heart failure, myocardial infarction, pneumonia, decompensated diabetes mellitus, cachexia, etc.). 3. Autoimmune diseases, a tendency to bleeding, a history of sepsis. 4. Oncological diseases. 5. The presence of acute or exacerbation of the chronic inflammatory process of the sinuses or oral cavity. 6. A positive result for HIV, hepatitis B (HBV), hepatitis C (HCV), syphilis (RW). 7. Cognitive deficit. 8. Mental disorders - hallucinations, behavior disorders. 9. Depression of a pronounced degree (not more than 19 points on the Hamilton scale). 10. Alcoholism, drug addiction, criminal liability in the patient's history. 11. Pregnancy, lactation.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Autologous mesenchymal stem cells
Autologous mesenchymal stem cells
Other:
Placebo
Saline solution

Locations

Country Name City State
Belarus the Belarusian Medical Academy of Postgraduate Education Minsk

Sponsors (1)

Lead Sponsor Collaborator
Belarusian Medical Academy of Post-Graduate Education

Country where clinical trial is conducted

Belarus, 

References & Publications (1)

Boika A, Aleinikava N, Chyzhyk V, Zafranskaya M, Nizheharodava D, Ponomarev V. Mesenchymal stem cells in Parkinson's disease: Motor and nonmotor symptoms in the early posttransplant period. Surg Neurol Int. 2020 Nov 11;11:380. doi: 10.25259/SNI_233_2020. eCollection 2020. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary motor symptoms change Positive trend is going to be detected in the overall score of the third part of the UPDRS scale(Unified Parkinson Disease Rating Scale) in the off- and in the on-period:neurological examination of patients in the dynamics is carried out in the morning after a 12 (24) - hour break in taking anti-Parkinsonian drugs "off-state", then one hour after they were taken "on-state".
A score of 64 on the third part of the UPDRS scale represents the worst (total motor disability) with a score of zero representing (no disability).
3 month
Primary non-motor symptoms change Identification and assessment of the severity of non-motor symptoms is carried out using Non-motor Symptoms Questionnaire (PD NMS Questionnaire).A score of 30 represents the worst result with a score of zero representing (no disability). 3 month
Primary sleep quality change The Pittsburgh Sleep Quality Index (PSQI) is used to assess sleep quality over the last month.The sleep component scores are summed to yield a total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality. 3 month
Primary daytime sleepiness change The Epworth Sleepiness Scale (ESS) is used to measure daytime sleepiness.The ESS score can range from 0 to 24. The higher the ESS score, the higher that person's average sleep propensity in daily life (ASP), or their 'daytime sleepiness'. 3 month
Primary signs of depression change We use the Hamilton Depression Scale - Hamilton psychiatric rating scale for depression (HDRS) - to identify signs of depression. A score of 52 represents the worst result with a score of zero representing (no disability). 3 month