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Recruiting NCT07245979

NCT07245979 Supplementation With Sirtuin Activators in Women With Increased Body Weight

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Clinical Trial Summary
NCT ID NCT07245979
Status Recruiting
Phase —
Sponsor Poznan University of Life Sciences
Condition Obesity & Overweight
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-10-08
Primary Completion 2026-11-30

Eligibility & Interventions

Sex Female only
Min Age 40 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Sirtuin activatorsPlacebo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-10-08 with a primary completion date of 2026-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this clinical trial is to learn if the six-month supplementation with sirtuin activators can affect metabolism in 40-to-65-year old women with increased body weight. The main questions it aims to answer are: Does sirtuin activators affect lipid and carbohydrate metabolism? Does sirtuin activators affect oxydative stress, immune functions and cell ageing? Researchers will compare sirtuin activators to a placebo (a look-alike substance that contains no drug) to see if drug sirtuin activators works to improve metabolic status. Participants will: Take sirtuin activators or a placebo every day for 6 months. Visit the university once every 3 months for checkups and tests.

Eligibility Criteria

Inclusion Criteria: * females * age: 40-65 years * overweight or obese: BMI \>25 kg/m2 Exclusion Criteria: * males * BMI \< 25 kg/m2 * sirtuin activators administration for 3 months prior to study * pregnancy or breastfeeding * recent dieting or being on calorie restricted diet * receiving pharmacotherapy to treat obesity, diabetes or hyperlipidemia * post-bariatric surgery * diabetes * cancer * chronic kidney, liver or autoimmune diseases * alcohol addiction

Contact & Investigator

Central Contact

Agata Chmurzynska, Professor

✉ agata.chmurzynska@up.poznan.pl

📞 +486184661

Principal Investigator

Agata Chmurzynska, Professor

PRINCIPAL INVESTIGATOR

Poznan Univeristy of Life Sciences

Frequently Asked Questions

Who can join the NCT07245979 clinical trial?

This trial is open to female participants only, aged 40 Years or older, up to 65 Years, studying Obesity & Overweight. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07245979 currently recruiting?

Yes, NCT07245979 is actively recruiting participants. Contact the research team at agata.chmurzynska@up.poznan.pl for enrollment information.

Where is the NCT07245979 trial being conducted?

This trial is being conducted at Poznan, Poland.

Who is sponsoring the NCT07245979 clinical trial?

NCT07245979 is sponsored by Poznan University of Life Sciences. The principal investigator is Agata Chmurzynska, Professor at Poznan Univeristy of Life Sciences. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology