Skip to content

Effect of resveratrol on aging among elderly adults

Safety and Effectiveness of Resveratrol in Promoting Sirtuin 1 Activation and Enhancing Health in Elderly Adults: A Prospective Interventional Approach - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084284
Enrollment
30
Registered
2025-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: E888- Other specified metabolic disorders

Interventions

Intervention1: Resveratrol: Resveratrol 500mg/day for 90 days(3months) Control Intervention1: NIL: NIL

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Men and women of age 60-75 years. If diabetic, should be on stable oral hypoglycemic medications for at least 3 months. If hypertensive, on stable anti-hypertensive medications for at least 3 months. Willing to give written informed consent.

Exclusion criteria

Exclusion criteria: Severe respiratory or cardiac dysfunction. Abnormally elevated liver enzymes ALT and or AST more than tree times ULN. eGFR less than thirty ml per min Elevated creatinine phosphokinase CPK more than three times ULN. Chronic alcoholic or drug abuse subjects. Known cases of malignancy and HIV infection. Use of antioxidant supplements. Use of Hormone replacement therapy. History of significant head injury or any major surgery. Previous use of resveratrol in the past three months. Severe cognitive impairment or dementia. Subject who participated in any other clinical investigation using an experimental drug in the past three months. Participants who are not willing to attend treatment schedule regularly

Design outcomes

Primary

MeasureTime frame
To assess then effect of resveratrol on sirtuin 1 during the study period Gradual recovery from symptomsTimepoint: Measurement of sirtuin 1 on day 0, day 45 and day 90

Secondary

MeasureTime frame
To find out the MoCa score improvement Six-minute Walk test (6MWT) Quality of life measurement (EuroQol-5D-5L Questionnaire) To evaluate adverse events during the study period To evaluate treatment adherenceTimepoint: Assessment of MoCa score, six-minute walk test, EuroQol 5D 5L Questionnaire on day 0, day 45, day 90

Countries

India

Contacts

Public ContactSubhiksha S

SRM hospital and research centre,SRM IST

melving@srmist.edu.in9080281508

Outcome results

None listed

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