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Effect of Suprabrain , A Polyherbal Formulation on Memory

A Randomized Double-blind Placebo-Controlled Trial To Evaluate Efficacy And Safety Of Suprabrain , A Polyherbal Formulation On Cognitive Function - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106477
Enrollment
96
Registered
2026-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: G988- Other disorders of nervous system

Interventions

Intervention1: Suprabrain: [containing extracts of Jyotisha mati 100mg, Shankspuspi 100 mg, Ashwagandha 50 mg, Brahmi 100 mg, Ginkgo biloba 50 mg and Rhodiola Rosea 100 mg] 500 mg twice a day Control

Sponsors

M/s Enkel Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18- 70 years of either sex 2. Able and willing to provide informed consent 3. Subject experiencing subjective cognitive complaints (e.g., forgetfulness, reduced attention, mental fatigue), confirmed by clinician. 4. Subject diagnosed with Attention Deficit Hyperactivity Disorder (ADHD), Autism Spectrum Disorder (ASD), Dementia, Stroke, Parkinson Disease, Alzheimer s Disease. 5. Patient diagnosed with mild to moderate severity of the specified diagnosis. 6. Capable of completing study questionnaires with or without minimal assistance.

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to ingredients of Suprabrain 2. History of drug and alcohol abuse 3. Serious uncontrolled systemic illnesses (e.g., active infection, severe hepatic/renal impairment) 4. Participation in another clinical study within the last 30 days 5. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Changes in Mini Mental Scale ExaminationTimepoint: 0, 4, 8 and 12 weeks

Secondary

MeasureTime frame
Cognitive failure questionnaire, Pittsburgh sleep quality index, Depression Anxiety Stress Scales - 10 item version, WHOQOL-BREF, PSS-10, Anxiety self-rating scale, Serum BDNF, serum NGF.Timepoint: 0, 4, 8 and 12 weeks

Countries

India

Contacts

Public ContactDebasish Hota

AIIMS, Bhubaneswar

pharm_debasish@aiimsbhubaneswar.edu.in9438884190

Outcome results

None listed

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