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NCT06989177Toboroz

Probiotic Intervention on Body Weight

An Interventional Study Investigating the Effects of Probiotics on Body Weight and Metabolic Homeostasis

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. márc. 17.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

This study is a randomized controlled trial with 120 overweight or obese (body-mass index, BMI, ≥ 24 kg/m²) participants and 20 normal-weight participants. Twelve weeks of energy-restricted nutritional and lifestyle intervention with placebo, Lactobacillus paracasei LC-19 (LC-19), or semaglutide (a glucagon-like peptide-1 receptor agonist, GLP-1RA) will be randomly conducted in the overweight or obese participants. The primary goal is to clarify the roles of LC-19 and semaglutide in weight reduction and in improving energy, glucose, and lipid metabolism, while also comparing side effects, adverse events, and long-term outcomes such as weight regain between these two interventions. In addition, the study will explore key factors affecting intervention response to provide evidence for optimizing individualized intervention strategies.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
140 (tervezett)
Első benyújtás
2025. máj. 6.
Kezdés
2025. jún. 10.
Elsődleges befejezés
2026. dec. 30.
Fő szponzor
Chinese Academy of Sciences
Betegségek
Elhízás
NCT-szám
NCT06989177

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 140
  • 2025. jún. 10. és az elsődleges befejezés (2026. dec. 30.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Self-reported weight change of more than 5 kg within the 90 days prior to screening.
  • Use of antibiotics, antimicrobials, or anti-inflammatory/analgesic salicylates (e.g., aspirin) within the 3 months prior to screening for 3 days or more.
  • Use of estrogen therapy or other hormonal medications within the past 6 months.
  • Underwent surgery within the past year (excluding appendectomy or hernia repair).
  • Severe cardiovascular or cerebrovascular diseases (e.g., heart failure, myocardial infarction, stroke, acute myocarditis, severe arrhythmia, or receiving interventional therapy).
  • Cancer or having received radiation or chemotherapy within the past 5 years.

Más betegség

  • Gastrointestinal diseases affecting digestion and absorption (e.g., severe diarrhea, severe constipation, severe inflammatory bowel disease, peptic ulcer, gallstones, cholecystitis).
  • Presence of metallic implants such as a cardiac stent or pacemaker.
  • Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia, or a personal history of hyperthyroidism or hypothyroidism.
  • Positive hepatitis B surface antigen (HBsAg), active tuberculosis, HIV, or other infectious diseases.
  • Any psychiatric disorder such as attention-deficit/hyperactivity disorder (ADHD), bipolar disorder, or epilepsy (including current use of antiepileptic medications), or use of antidepressant medications.

Laborértékek

  • Abnormal metabolic indicators (meeting any one of the following criteria is grounds for exclusion):
    • Normal weight (18.5 kg/m² ≤ BMI < 24 kg/m²):
    • Waist circumference ≥ 90 cm for men or ≥ 85 cm for women.
    • Fasting glucose ≥ 6.1 mmol/L or 2-hour postprandial glucose ≥ 7.8 mmol/L, or a confirmed diagnosis of diabetes.
    • Systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85 mmHg, or currently under antihypertensive treatment.
    • Fasting triglycerides (TG) ≥ 1.7 mmol/L; high-density lipoprotein cholesterol (HDL-C) < 0.9 mmol/L in men or < 1.0 mmol/L in women.
    • Overweight or obese (BMI ≥ 24 kg/m²):
    • Fasting plasma glucose > 11.1 mmol/L or HbA1c > 9%, or previously diagnosed diabetes, or currently using insulin or any antidiabetic medication.
    • Blood pressure ≥ 160/100 mmHg, or clinically diagnosed stage 2 or stage 3 (moderate or severe) hypertension, or currently under antihypertensive treatment.
    • Use of lipid-lowering drugs (e.g., fibrates, bile acid sequestrants, statins, PCSK9 inhibitors) within the past 3 months, or TG ≥ 5.7 mmol/L, or LDL ≥ 4.9 mmol/L.
  • Severe liver or kidney dysfunction (ALT, AST, or serum creatinine exceeding 3 times the upper limit of normal, UACR ≥ 30 mg/g, or eGFR < 60 mL/min).

Egyéb

  • Pregnancy or lactation.
  • Use of GLP-1 receptor agonists or probiotics within the past 3 months.
  • Heavy alcohol consumption (females > 40 g/day, approximately 250 mL of huangjiu [yellow rice wine], or 1000 mL of beer, or 100 mL of liquor per day; males > 80 g/day).
  • Chronic or acute pancreatitis.
  • Currently participating in another clinical study or having done so within the past 3 months.
  • Claustrophobia.
  • Inability to read, write, operate a smartphone, or perform daily activities independently.

Kiket keres a vizsgálat

  • Aged 20 to 50 years.
  • Normal-weight participants: 18.5 kg/m² ≤ Body Mass Index (BMI) < 24 kg/m².
  • Overweight or obese participants:
    • BMI ≥ 28 kg/m², or 24 kg/m² ≤ BMI < 28 kg/m² and a clinical diagnosis meeting semaglutide treatment indications (e.g., hyperglycemia, hypertension, dyslipidemia, fatty liver, obstructive sleep apnea, cardiovascular disease, etc.).
  • Willingness to participate in this study and provide signed informed consent.

Életkor a regiszterben: 20 év – 50 év · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Hangzhou Institute for Advanced Study, University of Chinese Academy of SciencesHangzhouKínaToboroz

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