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Safety evaluation and effect of consumption of Mulberry Capsule on the alterations of clinical symptoms and ischemic stroke biomarkers in transient ischemic attack and ischemic stroke patients

Safety evaluation and effect of consumption of Mulberry Capsule on the alterations of clinical symptoms and ischemic stroke biomarkers in transient ischemic attack and ischemic stroke patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201222006
Enrollment
60
Registered
2020-12-22
Start date
2021-08-30
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

transient ischemic attack Ischemic stroke Brain Supplement Mulberry transient ischemic attack Ischemic stroke

Interventions

Subjects are received the placebo product which has same color and smell look like product of Mulberry capsule ,Subjects are received product of Mulberry capsule 1000 mg/day,Subjects are received prod
medication plus placebo,medication plus Mulberry capsule 1000 mg/day,medication plus Mulberry capsule 2000 mg/day

Sponsors

Health Systems Research Institute, Thailand (HSRI)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Acute ischaemic stroke within the past 5-10 days that caused hemiparesis or hemiplegia 2. Aged between 18 years and 70 years 3. Fugl-Meyer motor scale (FMMS) scores of 55 or less at baseline

Exclusion criteria

Exclusion criteria: 1. Post rt-PA 2. Severe post-stroke disability (NIHSS score >20) 3. Previous stroke with motor deficit, comprehension deficits (aphasia) 4. Previous depression or MADRS score of more than 19; taking antidepressant drugs, monoamine oxidase inhibitors, neuroleptic drugs, or benzodiazepines during the month before inclusion 5. Undergoing carotid endarterectomy 6. Pregnancy 7. Major diseases that would prevent follow-up. Enrolment, follow-up

Design outcomes

Primary

MeasureTime frame
The changes of hematological and clinical chemistry parameters 6 weeks laboratory

Secondary

MeasureTime frame
vascular cell adhesion molecule1(VCAM-1) 6 weeks ELISA Kit ,Matrix metalloproteinases 9 (MMP-9) 6 weeks ELISA Kit ,VonWillebrand Factor (VWF) 6 weeks ELISA Kit ,S100β 6 weeks ELISA Kit ,Safety evaluation and side effect 6 weeks Questionair,Electrocardiogram 6 weeks electrocardiography equipment,NIHSS score 6 weeks Questionair,Stool examination (PH, Lactobacillus spp., Bifidobacterium spp. and Short chain fatty acid) 6 weeks laboratory

Countries

Thailand

Contacts

Public ContactSupaporn Muchimapura

Khon Kaen University

supmuc@kku.ac.th6667925420

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026