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NCT06019117Befejeződött

Effectiveness of Probiotic K10 in Managing Health Outcomes in Parkinson and Alzheimer Disease

Effectiveness of a Probiotic K10 in Managing Health Outcomes in Parkinson's Disease and in Early Stage (Mild Cognitive Impairment to Mild Dementia) and Alzheimer's Disease

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. júl. 30.

Rövid összefoglaló (regiszter, angolul)

Evaluation of the effects of the K10 probiotic mix in patients with degenerative neurological diseases (Parkinson and Alzheimer's) with a focus on cognitive, motor and psychiatric neurological evaluation. Single-centre, double-blind, placebo-controlled randomized clinical trial (RCT), Interventional Model: Parallel Assignment, phase III study. Two groups will be composed, with two arms each, 1 group composed of patients with Parkinson's and 1 group with patients with Alzheimer's, 52 patients in each group. The first arm of each group will receive placebo and the other arm of each group will receive the mix K10. In this study, researchers will conduct a randomized, placebo-controlled, phase III trial of a probiotic preparation (Probiotic K10) to evaluate its use as a viable treatment option for neurodegenerative disorders, including Parkinson's disease (PD) and Alzheimer's disease. of Alzheimer (AD). This formulation has been previously demonstrated to improve cognitive function, systemic inflammation, systemic oxidative stress in Alzheimer's patients. The main objective of this study is to compare its effect with placebo on cognitive status in individuals with AD and PD, the UPDRS total score in people with early PD and quality of life, and the measurement of caregiver burden in AD and PD. Participants will be randomly assigned to receive a placebo (an inactive substance) and a K10 probiotic (dose 30.000.000 CFU/day). They will be evaluated at baseline, 45 days and 90 days.

Állapot (regiszter)
Befejeződött
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
104 (tényleges)
Első benyújtás
2023. aug. 17.
Kezdés
2023. aug. 10.
Elsődleges befejezés
2023. nov. 25.
Fő szponzor
Deivis de Oliveira guimaraes
NCT-szám
NCT06019117

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Bevont résztvevők: 104
  • 2023. aug. 10. és az elsődleges befejezés (2023. nov. 25.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

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Korábbi kezelés

  • Parkinsonism due to drugs including neuroleptics, alpha-methyldopa, reserpine, metoclopramide, valproic acid.
  • Sufficient deficiency to require changes in dopaminergic medication treatment during follow-up compared to baseline treatment schedule.
  • Unstable dose of active CNS therapies.
  • Participation in other drug studies or use of other investigational drugs within 30 days prior to the Screening Visit.
  • History of structural brain disease, such as previous trauma causing damage detected on a CT scan or MRI, hydrocephalus, or previous brain neoplasms.
    • Alzheimer's Exclusion Criteria:
  • Use of any investigational agents within 30 days prior to screening
  • Major surgery within 8 weeks prior to the Baseline Visit

Más betegség

  • Other parkinsonian disorders.
  • History of symptomatic stroke.
  • Other severe and uncompensated illnesses, including severe psychiatric illnesses.
  • Patients with active cardiovascular, restrictive peripheral vascular, or cerebrovascular disease in the past year.
  • History of active epilepsy within the past 5 years.
  • History of electroconvulsive therapy.
  • History of any brain surgery for Parkinson's disease.
  • Significant neurological disease such as Parkinson's disease, stroke, brain tumor, multiple sclerosis, or seizure disorder
  • Major depression treated in the past 12 months, major mental illness such as schizophrenia, or recent (in past 12 months) alcohol or substance abuse
  • History of invasive cancer within the past two years (excluding non-melanoma skin cancer)
  • Uncontrolled cardiac conditions or severe unstable medical illnesses
  • Antiretroviral therapy for human immunodeficiency virus (HIV)
  • Conditions that will contribute to oxidative stress: current cigarette or cigar smokers (within past month), diabetics on insulin or poorly controlled on oral hypoglycemics

Egyéb

  • Parkinson's Exclusion Criteria:
  • Use of antioxidants (such as selegiline, rasagiline, vitamins E and C), additional supplemental vitamins or minerals, regular use of neuroleptics, chloramphenicol, valproic acid, warfarin.
  • Modified Hoehn and Yahr score of 3 or more on Screening Visit or Baseline Visit.
  • UPDRS tremor score of 3 or greater at Screening Visit or Baseline Visit.
  • Use of appetite suppressants within 60 days of the Baseline Visit.
  • Blindness, deafness, language difficulties or any other disability which may prevent the participant from participating or cooperating in the protocol.

Kiket keres a vizsgálat

  • Eligibility criteria for individuals with Parkinson's. Ages eligible to participate in the study: 18 years or older Accept healthy volunteers: No. Gender Eligibility for Study: All genders
  • Presence of all 3 cardinal features of Parkinson's disease (tooth tremor, bradykinesia, and rigidity). Clinical signs must be asymmetrical.
  • Diagnosis of Parkinson's disease within 5 years of the Screening Visit.
  • Age 18 years or older.
  • Women must not be of childbearing potential or must use an approved form of contraception during the trial period.
    • Eligibility Criteria for Individuals with Alzheimer's. Eligible ages to participate in the study: 60 -85 years Accept healthy volunteers: No. Gender Eligibility for Study: All genders
  • Men or women between the ages of 60 and 85
  • Diagnosis of probable Alzheimer's disease
  • Portuguese-speaking, English-speaking; Spanish-speaking if the individual site allows
  • Study partner or caregiver to ensure compliance
  • Mini-Mental State Exam score at screening visit greater than 14
  • Stable medical condition for 3 months prior to screening, with no significant abnormal liver, kidney, or blood studies.
  • Able to take oral medications
  • Modified Hachinski Ischemic Index less than or equal to 4
  • CT or MRI from the onset of memory impairment, demonstrating the absence of a clinically significant focal lesion
  • Physically acceptable for this study, as confirmed by medical history, physical examination, neurological examination, and clinical testing

Életkor a regiszterben: 18 év – 85 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

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