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The ameliorative effects of probiotics on aging-related phenotypes

Clinical Randomized Controlled Trial Evaluating the Intervention Effects of Probiotics on Aging-Related Phenotypes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112293
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Aging

Interventions

Longer Telomere Group:None
Shorter Telomere Group:None
Placebo group:Oral placebo, once daily, for 3 months
Probiotics group:Oral probiotics, once daily, for 3 months
Postbiotic group:Oral postbiotic, once daily, for 3 months

Sponsors

Jingdezhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 55 and 79 years;2. Healthy adults with no diagnosis of severe chronic diseases;3. Non-smokers or former smokers, and non-heavy drinkers, to minimize the impact of other factors on the aging process;4. Participants must undergo a comprehensive health assessment prior to enrollment, including blood tests, electrocardiogram (ECG), etc., to ensure the absence of severe systemic diseases;5. Have not taken laxatives, oral antibiotics, probiotics, or other drugs that may alter the gut microbiota within one month;6. Understand the intervention process and sign the informed consent form (ICF).

Exclusion criteria

Exclusion criteria: 1. Patients with severe chronic diseases such as cardiovascular, renal, or hepatic diseases that may affect the aging process;2. Patients on long-term use of antibiotics, hormones, or other drugs that may disrupt the balance of the gut microbiota;3. Patients allergic to probiotic ingredients;4. Patients with severe unhealthy lifestyles, such as heavy drinking, drug abuse, and other related behaviors;5. Pregnant or lactating women;6. Patients diagnosed and evaluated by clinical physicians as unsuitable for probiotic adjuvant therapy.

Design outcomes

Primary

MeasureTime frame
Aging-related phenotypes;Gut microbiota composition;Gut metabolomic profile;

Countries

China

Contacts

Public ContactMinyan Chen

Jingdezhen Second People's Hospital

2507823306@qq.com+86 139 7986 8355

Outcome results

None listed

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