Clinical trial registry record

Impact of Regular Consumption of Grapes on Eye Health in Singapore Older Adults

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Unknown.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated November 9, 2023.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05064865
Last registry update
November 9, 2023
Status
Unknown
Phase
Phase not reported
Sponsor
National University of Singapore
Enrollment
34
Countries
Singapore
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Unknown. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · PREVENTION · DOUBLE
Evidence population
Human clinical study registration
Participants
34
Population
ALL · 60 Years to 85 Years
Duration
2022-01-28 to 2024-10-01
Intervention
Freeze-dried table grape powder; Placebo of the table grape powder
Comparator
Placebo grape powder
Outcomes measured
Change in macular pigment optical density — Every four weeks (week 0, week 4, week 8, week 12, week 16); Change in skin carotenoid status — Every four weeks (week 0, week 4, week 8, week 12, week 16); Change in blood carotenoid concentration — Every eight weeks (week 0, week 8, week 16); Change in flow mediate dilation — week 0 and week 16; Change in endothelial function — week 0 and week 16; Change in the concentration if Endothelin-1 in plasma — week 0 and week 16; Change in the concentration if Nitric Oxide in plasma — week 0 and week 16; Change in body weight — Every four weeks (week 0, week 4, week 8, week 12, week 16); Change in BMI — Every four weeks (week 0, week 4, week 8, week 12, week 16); Change in blood pressure — Every four weeks (week 0, week 4, week 8, week 12, week 16); change in waist circumference — Every four weeks (week 0, week 4, week 8, week 12, week 16); Change in the concentration of malondialdehyde in plasma — Every eight weeks (week 0, week 8, week 16); Change in the concentration of 8-iso-prostaglandin F2α in plasma — Every eight weeks (week 0, week 8, week 16); Change in blood glucose concentration — Every eight weeks (week 0, week 8, week 16); Change in total cholesterol — Every eight weeks (week 0, week 8, week 16); Change in high-density lipoprotein cholesterol — Every eight weeks (week 0, week 8, week 16); Change in low-density lipoprotein cholesterol — Every eight weeks (week 0, week 8, week 16); Change in total triglyceride — Every eight weeks (week 0, week 8, week 16)
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Vision ageing · 100%Abstract contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Title supplies longevity context: older adult. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.