Tocotrienols for Obesity of Postmenopausal Women

Running, not enrolling · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Obesity, Postmenopausal Women

In brief

Postmenopausal women are at a risk of excessive weight gain, bone loss, hypertension, and metabolic syndrome. Obesity-induced chronic low-grade inflammation is initiated by excess nutrients in metabolic cells. Recent studies have indicated tocotrienols (one kind of vitamin E, a potent antioxidant) supplement may be good for mitigating negative impacts of obesity in postmenopausal women. The purpose of the study is to examine the effect of 24-week tocotrienols on obesity-associated outcome measurements in postmenopausal women. The investigators will enroll 60 qualified women at the start of the study and randomly assigned to no tocotrienols (placebo) or tocotrienols group for 24 weeks. Obesity-associated measurements will be recorded using blood, urine, adipose tissue, and fecal samples. All data will be analyzed statistically.

Key facts

Study ID
NCT03705845
Run by
Texas Tech University Health Sciences Center
People needed
60
Starts
2019-03-15
Expected to finish
2025-12-30
Last updated by the study team
2025-03-28

Who can join

Age: any. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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