LA Improves the Prognosis of Patients With ICVD

Sponsor
Huaqiu Zhang (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05845983
Collaborator
(none)
236
2
67.9

Study Details

Study Description

Brief Summary

Ischemic cerebrovascular disease will cause serious harm to the life and safety of patients, and the treatment prognosis is poor. Numerous clinical trials have demonstrated that probiotics can improve cognitive function in people under multimodal. We have previously found that Lactobacillus acidophilus administration could improve cognitive impairment in MCAO and BCAS mice. Therefore, Based on the above research background and the basis of previous studies, we believe that the administration of Lactobacillus acidophilus solid drink (pure Lactobacillus acidophilus strain) can improve the cognitive function of patients with cerebral ischemia through the "brain-gut axis".

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Lactobacillus acidophilus
  • Dietary Supplement: Maltodextrin
N/A

Detailed Description

Ischemic cerebrovascular disease, as a common form of stroke, is one of the main causes of global morbidity and mortality. The mortality rate of this disease is relatively high, and the treatment prognosis is poor, which will cause serious harm to the life and safety of patients. The optimal treatment for ischemic cerebrovascular disease is still unclear, and the effects of different treatments are still controversial. Therefore, it is of great clinical significance to explore a safe and simple adjuvant treatment method to help patients recover their nervous system function faster and better.

At present, numerous clinical trials have demonstrated that probiotics can improve cognitive function in people under multimodal. Adding intestinal probiotics can improve the intestinal flora distribution, and significantly improve cognitive function in elderly patients with mild cognitive impairment and prevention of brain atrophy. Lactobacillus acidophilus is rich in short chain fatty acids (SCFA). Clinical studies have shown that SCFA levels are negatively correlated with the severity and prognosis of ischemic stroke. Numerous studies have demonstrated that the intestinal supply short chain fatty acids can improve cognitive function, in the middle cerebral artery occlusion (MCAO) induced by acute cerebral ischemia model, rich in the intestines of SCFA can cure acute cerebral ischemia in mice induced by nerve injury. More importantly, in mice with acute cerebral ischemia induced by middle cerebral artery occlusion (MCAO) and chronic cerebral ischemia caused by bilateral common carotid artery stenosis (BCAS), we have previously found that mice have cognitive impairment, accompanied by intestinal flora dysregulation.

Lactobacillus acidophilus administration has a significant effect on improving cognitive function. Based on the above research background and the basis of previous studies, the researchers believe that the administration of Lactobacillus acidophilus solid drink (pure Lactobacillus acidophilus strain) can improve the cognitive function of patients with cerebral ischemia through the "brain-gut axis", and increase the reliability and scope of revascularization, and ultimately improve the prognosis of patients with ischemic cerebrovascular disease.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
236 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Lactobacillus Acidophilus Improves the Prognosis (Cognitive Function) of Patients With Ischemic Cerebrovascular Disease After Surgery: a Multicenter, Prospective, Three-blind, Placebo-randomized Controlled Study
Anticipated Study Start Date :
May 4, 2023
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
Dec 31, 2028

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Control group

The patient received conventional treatment and Maltodextrin treatment (placebo) for three months after surgery.

Dietary Supplement: Maltodextrin
Maltodextrin solid drink (food grade, MD20, Shandong Zhongke Jia-yi Biological Engineering Co., LTD.), 3g, twice a day, once in the morning and once in the evening, 1 bag each time, by drinking water, direct oral intake, 1 month/course, continuous use for three courses.

Experimental: LA treatment group

The patient received conventional treatment and Lactobacillus acidophilus treatment for three months after surgery.

Dietary Supplement: Lactobacillus acidophilus
Lactobacillus acidophilus solid drink (pure bacteria, food grade, JYLA-191, Shandong Zhongke Jia-yi Biological Engineering Co., LTD.), 3g (containing 2*10^10CFU), twice a day, once in the morning and once in the evening, 1 bag each time, by drinking water, direct oral intake, 1 month/course, continuous use for three courses.

Outcome Measures

Primary Outcome Measures

  1. Mini-mental State Examination (MMSE, 0-30) scale [Three months.]

    Higher scale scores mean better cognitive function.

  2. Montreal Cognitive Assessment (MoCA, 0-30) scale [Three months.]

    Higher scale scores mean better cognitive function.

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Between 35 and 65 years old;

  2. Han nationality;

  3. Diagnosed as ischemic cerebrovascular disease with mild to moderate symptoms;

  4. Can communicate normally, complete neuropsychological tests independently, and sign informed consent;

  5. No previous surgical history;

  6. No contraindications such as PET, MRI and DSA;

  7. No history of stroke identified by imaging;

  8. No family history of other chronic diseases, cancer, mental illness or dementia;

  9. Improved Rankin scale score ≤2;

  10. Ischemic symptoms appeared in the carotid area ≤3 months before the visit;

  11. In line with the surgical treatment of ischemic cerebrovascular disease;

Exclusion Criteria:
  1. previous dementia;

  2. hearing or visual impairment;

  3. Drugs that may or are known to influence cognitive abuse;

  4. alcohol addiction;

  5. Diagnosis of depression, schizophrenia and other psychiatric diseases;

  6. MRI showed severe cerebral infarction;

  7. Those allergic to Lactobacillus acidophilus;

  8. Baseline CT showed intracranial hemorrhage;

  9. ischemic onset accompanied by epilepsy;

  10. illiteracy;

  11. pregnancy or breastfeeding;

  12. any serious medical condition that may interact with treatment;

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Huaqiu Zhang

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Huaqiu Zhang, Professor, Tongji Hospital
ClinicalTrials.gov Identifier:
NCT05845983
Other Study ID Numbers:
  • TJ-IRB20230304
First Posted:
May 6, 2023
Last Update Posted:
May 6, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2023