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RecruitingNCT07245979Updated May 22, 2026

Supplementation With Sirtuin Activators in Women With Increased Body Weight

An interventional study of Sirtuin activators and Placebo in Obesity & Overweight, sponsored by Poznan University of Life Sciences. Recruiting at 1 site in Poland. Open to female participants aged 40 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by Poznan University of Life Sciences · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
40 Years to 65 Years
Sex
Female
01

Study 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.

02

Conditions studied

  • Obesity & Overweight
03

In context

Obesity

11,522 studies on the registry are indexed under Obesity; 2,033 are open to participants now.

This study's planned enrollment of 120 is above the median of 67 across 9,006 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Poznan University of Life Sciences is the lead sponsor of 25 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • females
  • age: 40-65 years
  • overweight or obese: >25 kg/m2

Exclusion criteria

Exclusion Criteria:

  • males
  • \< 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 diseases
  • alcohol addiction
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Experimental: sirtuin activators

    Sirtuin activators supplementation for 6 months, daily dose of 1278 mg, taken twice a day in a capsulated form. Daily dose will contain: resveratrol - 500 mg, leucin - 467 mg, Epigallocatechin gallate - 100 mg, quercetin - 100 mg, curcuminoids - 100 mg, niacin 10.7 mg. Daily number of capsules will be 2 x 2 = 4.

    Dietary Supplement: Sirtuin activators

  • Placebo comparator
    Placebo comparator: placebo

    Placebo will be an inactive substance (maltodextrin) provided in the same-looking capsules as sirtuin activators. Placebo will be administered twice a day, daily number of capsules will be 2 x 2 = 4.

    Dietary Supplement: Placebo

Interventions

  • Dietary supplementSirtuin activators

    Sirtuin acitivators supplementation for 6 months

  • Dietary supplementPlacebo

    Placebo supplementation for 6 months

06

What researchers measure

Primary outcomes

  1. Concentrations of blood lipids

    Total cholesterol, Triacyglycerols, low density lipoprotein (LDL) cholesterol, high density lipoprotein (HDL) cholesteroll

    Time frame: 6 months, two measurements: at month 0 and 6

  2. Blood glucose concentrations

    Blood glucose concentration

    Time frame: 6 months, two measurements: at month 0 and 6

  3. Ageing biomarkers: transcription level of the p16INK4a gene in peripheral blood mononuclear cells

    transcription level of the p16INK4a gene in peripheral blood mononuclear cells

    Time frame: 6 months, two measurements: at month 0 and 6

  4. Ageing biomarkers: telomere lenght

    telomere lenght measured in DNA isolated from whole blood

    Time frame: 6 months, two measurements: at month 0 and 6

  5. Ageing biomarkers: SA beta galactosidase activity

    SA beta galactosidase activity

    Time frame: 6 months, two measurements: at month 0 and 6

  6. Oxidative stress

    activities of oxidative stress enzymes in blood

    Time frame: 6 months, two measurements: at month 0 and 6

Secondary outcomes

  1. Body mass

    Measured in kg

    Time frame: 6 months, two measurements: at month 0, 3 and 6

  2. Body composition

    Body composition will include percent body fat and lean body mass measured with air displacement plethysmography

    Time frame: 6 months, two measurements: at month 0, 3 and 6

  3. Waist and hips circumference

    Measured in cm

    Time frame: 6 months, two measurements: at month 0, 3 and 6

  4. Genotype analyisis of the Sirt1 gene

    Nucleotite variants at certain genomic position will be analysed

    Time frame: baseline

07

Study locations

1 of 1 sites recruiting
  • Poznan University of Life Sciences
    Poznan, Poland
    Recruiting
    • Agata Chmurzynska, Professor · Contactagata.chmurzynska@up.poznan.pl · +486184661
    • Emilia Zawieja · Sub investigator
    • Monika Mlodzik-Czyzewska · Sub investigator
    • Marcin Sadowski · Sub investigator
    • Agata Jankowska · Sub investigator
    • Agnieszka Seremak-Mrozikiewicz · Sub investigator
    • Grażyna Kurzawińska · Sub investigator
    • Agata Muzsik-Kazimierska · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07245979
Lead sponsor
Poznan University of Life Sciences
Collaborators
Poznan University of Medical Sciences, NutroPharma
Responsible party
Agata Chmurzyńska (Professor, Poznan University of Life Sciences) — Principal investigator
First posted
Nov 24, 2025
Start date
Oct 8, 2025
Primary completion
Nov 30, 2026 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
May 22, 2026

Study contacts

Agata Chmurzynska, Professor
Contact
agata.chmurzynska@up.poznan.pl
+486184661
Agata Chmurzynska, Professor
principal investigator · Poznan Univeristy of Life Sciences

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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