Clinical trial registry record

Elderberry Functional Gum and Cognitive & Oral Health in Older Adults

A registered study indexed because it matched monitored longevity research terms. Registry status: Not Yet Recruiting. 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 Not Yet Recruiting.
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 July 8, 2025.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT07054645
Last registry update
July 8, 2025
Status
Not Yet Recruiting
Phase
Phase not reported
Sponsor
Burdur Mehmet Akif Ersoy University
Enrollment
34
Countries
Turkey (Türkiye)
Match confidence
80%
Source feed
ClinicalTrials.gov
Automated source synopsis

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

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · SUPPORTIVE CARE · DOUBLE
Evidence population
Human clinical study registration
Participants
34
Population
ALL · 65 Years
Duration
2025-11-01 to 2026-11-01
Intervention
Elderberry Anthocyanin Chewing Gum; Placebo Chewing Gum
Comparator
Placebo Arm Title
Outcomes measured
Change in Cognitive Function Assessed by MoCA (Montreal Cognitive Assessment) Score — Baseline and Week 6; Change in Executive Function Assessed by Stroop Test — Baseline and Week 6; Change in Alpha Diversity Assessed by Shannon Index — Baseline and Week 6; Change in Beta Diversity Assessed by UniFrac and Bray-Curtis Distances — Baseline and Week 6; Change in Salivary Flow Rate — Baseline and Week 6; Change in Salivary pH — Baseline and Week 6; Change in Salivary Total Antioxidant Capacity (FRAP Method) — Baseline and Week 6; Change in Salivary Total Phenolic Content (Folin-Ciocalteu Method) — Baseline and Week 6; Change in Salivary Streptococcus mutans Count — Baseline and Week 6; Change in Salivary Lactobacillus spp. Count — Baseline and Week 6; Product Acceptability Score (Hedonic Scale) — Initial Exposure and Week 6
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 · 80% 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.

  • Oral health and ageing · 80%Title contains controlled term: oral health. 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.