Lactobacillus Plantarum and Hormonal Regulation in Obese Women

Recruiting · NCT06987279 · Interventional (participants receive a specific treatment) · Lead sponsor: Wecare Probiotics Co., Ltd.

Interventions studied

To evaluate the regulatory effect of Lactobacillus plantans Lp90 formula on visceral fat metabolism and sex hormone balance in obese women.

Age range

18 Years to 40 Years

Sex

Female

Healthy volunteers

Yes - healthy volunteers may be accepted

Phase

Not applicable (e.g. observational or device study)

Study type

Interventional (participants receive a specific treatment)

Age: 18 to 40 years old, female, BMI ≥ 25 kg/m2.
Be willing to receive follow-up during the intervention period.
Be willing to provide two blood, urine and fecal samples during the intervention period.
Be willing to take the compound probiotics by oneself every day during the intervention period.
Have good hearing and be able to hear and understand all instructions during the intervention period.

Suffering from digestive system diseases, mainly gastrointestinal diseases (celiac disease, ulcerative colitis, Crohn's disease).
Suffering from severe neurological disorders (epilepsy, stroke, severe head trauma, meningitis within the past 10 years, brain surgery, brain tumor, long-term coma - excluding general anesthesia).
Have received/are currently receiving treatment for the following mental illnesses: alcohol/drug/substance abuse dependence, schizophrenia, psychosis, bipolar disorder.
Take medication for depression or low mood.
Suffering from internal organ failure (such as heart, liver or kidney failure, etc.).
Have received radiotherapy or chemotherapy in the past.
Have received general anesthesia surgery/procedures within the past three years, or plan to receive general anesthesia procedures/surgeries within the next three months during this trial.
Have suffered from hepatitis (hepatitis B, hepatitis C), HIV or syphilis in the past.

1 location listed.