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A clinical study to evaluate the advanatges and safety of long term CurQfen consumption in dementia patients

A clinical study to evaluate the efficacy and safety of Curcumin supplementation (CurQfen - The enhanced bio available formulation of curcumin) on Dementia patients having Mild to Moderate decline in Locomotor activities and impairment in Learning/Memory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012410
Enrollment
48
Registered
2018-03-07
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

Health Condition 1: null- Dementia

Interventions

Intervention1: CurQfen: Bioavailable form of curcumin - The CurQfen, 500mg 2 times in a day for 180 days Control Intervention1: Curcumin: Normal Curcumin 500mg ,2 times in a day for 180 days Control I

Sponsors

Akay Flavours and Aromatics Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 55-75 Years ( Both Inclusive) 2.Male and Female Subjects 3.Patients with a MMSE Score Less than 26 and More than 14 (Both are Inclusive) 4.Must have a caregiver to attend the study visit. 5.Informed consent from Subject and Legally acceptable Representative-LAR( LAR can be Spouse/Parent/Son/Daughter/Guardian/Person Having charge or any other legally acceptable Representative)

Exclusion criteria

Exclusion criteria: 1.Severe Memory Loss 2.Stroke 3.Psychiatric illness 4.Subjects who are under the treatment with anti Inflammatory Drugs 5.Objection from family members or any other close relatives or Legally acceptable representatives 6.If the participation in the study cause any harm to possible benefits to the patients, including Insurance benefits. 7.Objection from the Physician, under whom, current treatment is going on. 8.Patients, who are in the Clinicians judgment, are like to be placed in a nursing home, within next 6 months 9.Any condition that in Opinion of the Investigator, does not justify the Subjectsâ?? participation in the study.

Design outcomes

Primary

MeasureTime frame
Comparative changes in the MMSE, ACE-R, QOL,Beta Amyloid scores from baseline to Day 180.Timepoint: Day 0,Day 90,Day 180

Secondary

MeasureTime frame
Comparative changes in the anti oxidant, anti inflammatory and safety parameters from Day 0 To day 180Timepoint: Day 0. Day 90, Day 180

Countries

India

Contacts

Public ContactJestin V Thomas

Akay Flavours and Aromatics Private Limited

Krishnakumar.IM@akay-group.com04842686111

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 8, 2026