Mitochondrial / energy
Urolithin A
Mitophagy / mitochondrial quality control · Metabolite
Evidence at a glance
Each record keeps its own evidence class. Counts are records in this public edition, not a quality score.
Evidence gap: Route-specific human PK and absolute bioavailability are not established in the imported material.
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Records (4)
H
Human clinical / research
Human clinical / research
Human supplement literature reported
The guide reports human oral supplement data.
Context: Specific trial and primary identifier are not provided in this entry.
Limitations: This summary is not a primary-source efficacy or PK audit.
Route: Oral · Absolute bioavailability and formulation comparison are not established in this entry.
- Peptide Protocol Field Guide · version 7
Open this exact record in the library →Suggest a correctionHuman clinical / research
Oral daily pattern in supplement literature
Distinct protocol, timing or sequence preserved from the saved research material. Unreported fields remain unknown.
Context: Human · Human supplement trials described in the field guide
Human study regimen: Frequency: Daily; Route: Oral; Species: Human; Population: Human supplement trials described in the field guide
Limitations: No trial identifier, study-specific amount, formulation or duration is supplied. The private supplement-history amount is excluded.
Route: Oral
- Peptide Protocol Field Guide · version 7
Open this exact record in the library →Suggest a correctionHuman clinical / research
Urolithin A in older adults
Administration reported for this specific study or labeled indication.
Context: 66 older adults
Human study regimen: Amount: 1,000 mg; Route: Oral softgels; Frequency: Daily; Duration: 4 months; Species: Human; Population: 66 older adults
Limitations: No significant between-group difference in six-minute walk distance or maximal ATP production. Muscle endurance was a separate endpoint.
Route: Oral softgels
Open this exact record in the library →Suggest a correctionHuman clinical / research
Urolithin A in middle-aged adults
Administration reported for this specific study or labeled indication.
Context: Middle-aged adults
Human study regimen: Amount: 500 or 1,000 mg; Route: Oral; Frequency: Daily; Duration: 4 months; Species: Human; Population: Middle-aged adults
Limitations: Randomized dose arms with a placebo comparator. Muscle strength findings and other exercise endpoints should be interpreted separately.
Route: Oral
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Educational research summary. Study amounts are research context, not a dose recommendation. Not medical advice.