🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT06953518
Starting soon Not applicable

An Open-Label Pilot Study of Qualia Senolytic Supplementation for the Attenuation of Systemic Inflammatory Cytokines

NCT06953518 · tracked via the Priya Life Science USA tracker
Sponsor
Qualia Life Sciences
Phase
Not applicable
Started
2025-05-12
Last updated
2025-05-01

Condition(s) studied

Inflammation

Investigational drug(s) / intervention(s)

Qualia Senolytic

Qualia Senolytic: Qualia Senolytic manufactured by Qualia Life Science

Study summary

This open-label pilot study includes adults aged 45 to 79 residing in the United States. The study will last 7 days. Participants will provide blood samples via an at-home finger-prick kit at baseline and day 7 and complete electronic surveys on health indicators at baseline, and days 3 and 7. All procedures are conducted remotely, with no in-person visits, to collect real-world evidence.

Eligibility

Sex
ALL
Min age
45 Years
Max age
79 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Provide voluntary, written, informed consent to participate in the study * Agree to provide a valid cell phone number and are willing to receive communications through text. * Healthy adults 45 - 79 years of age Can read and write English * Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly. * Willing to self-administer the fingerstick test kit at home for both a baseline and post-intervention blood sample, and to complete a release form that gives NHC access to the results of these tests. * Willing to complete questionnaires, records, and diaries associated with the study. Exclusion Criteria: * Women who are pregnant, breastfeeding, or planning to become pregnant during the trial * Known food intolerances/allergy to any ingredients in the product * Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, cancer * Having had a significant cardiovascular event in the past 6 months * Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines * On immunosuppressive therapy * Individuals who were deemed incompatible with the test protocol * Adults lacking capacity to consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Qualia Life Sciences Carlsbad California

More Qualia Life Sciences trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06953518 on ClinicalTrials.gov ↗ ← All trials in the USA