Skip to content

An open randomized clinical study to evaluate the efficacy of Medhya gana vati in improving the cognition

An open randomized clinical study to evaluate the efficacy of Medhya gana vati in improving the cognition - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112604
Enrollment
80
Registered
2026-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

None listed

Interventions

None listed

Sponsors

Dr Vishnupriya Seetharam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Healthy volunteers aged between 18 years to 60 years with the symptoms of forgetfulness from either sex. 2)Healthy Volunteers with subjective complaints of memory loss confirmed by a cognitive assessment tool and signed the informed consent. 3)Healthy volunteers not under any other supplements for atleast 2 weeks prior to enrollment.

Exclusion criteria

Exclusion criteria: 1)Healthy volunteers below 18 years and above 60 years of age. 2)Healthy volunteers with diagnosed neurodegenerative disorders (Alzhiemers disease, parkinsons disease). 3)History of psychiatric illnesses, severe depression or any neuropsychiatric conditions. 4)Volunteers with epilepsy requiring anti convulsant therapy. 5)Volunteers with severe systemic illnesses (like uncontrolled diabetes, severe hypertension, hepatic/renal failure). 6)Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
to assess the change in values of the memory assessment scale scoresTimepoint: 30 days

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Vishnupriya Seetharam

The Glocal University

muralivaidyaka@yahoo.com9447141281

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026