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A clinical study to evaluate the efficacy of NEUROCAF in reducing the risk of developing Parkinsonâ??s disease.

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Study to Evaluate the Efficacy and Safety of NEUROCAF in healthy elderly subjects at risk of developing Parkinsonâ??s disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/09/027802
Enrollment
24
Registered
2020-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: NEUROCAF: Oral administration of single dose of NEUROCAF at the morning for 84 days Control Intervention1: Placebo: Oral administration of single dose of placebo at the morning for 84 d

Sponsors

Vidya Herbs Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Should not be an any medication for cognition and other neurological disorders 2. Post-menopausal women 3. Must be willing and able to give informed consent and comply with the study procedures.

Exclusion criteria

Exclusion criteria: 1. Subjects with history of Neurogenerative disorder, including Parkinsonâ??s disorder,Psychiatric disorders ,Uncontrolled / serious medical illness including diabetes, liver disease, hypertension,Cardiac Disease/Neurological Problems,Auto-immune disease (rheumatoid arthritis, lupus, type 1 diabetes),Gastrointestinal tract bleeding / peptic ulcer disease 2. Subjects having symptoms of viral infection, including COVID-19 infection 3. Subjects who may be allergic to any of the natural constituents of the Investigational Product. 4. Known HIV or Hepatitis B positive or any other immuno-compromised state 5. Subjects on any other medical or clinical investigation or on any nutrition supplements and dietary regime. 6. Subjects visually or mentally handicapped or having difficulty to communicate 7. History of clinically significant illness or any other medical disorder that may interfere with subject treatment, assessment or compliance with the protocol. 8. Currently participating or having participated in another clinical trial during the last 3 months prior to the beginning of this study. 9. Any additional condition(s) that in the Investigators opinion would warrant exclusion from the study or prevent the subject from completing the study.

Design outcomes

Primary

MeasureTime frame
Changes in Bio markers of Parkinsons DiseaseTimepoint: Day 0, Day 84

Secondary

MeasureTime frame
Changes in geriatric parameters Timepoint: Day 0, Day 42, Day 84;Safety of NEUROCAFTimepoint: Day 0, Day 42, Day 84

Countries

India

Contacts

Public ContactJestin V Thomas

Leads Clinical Research and Bio Services Pvt. Ltd

jestin.leadsclinbio@gmail.com9845125293

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026