Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT07103382

Efficacy and Safety of Attapulgite in Patients With Obesity: An Exploratory Clinical Trial

Led by Second Xiangya Hospital of Central South University · Updated on 2025-09-05

40

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To explore the safety and efficacy of attapulgite in the treatment of obese individuals or overweight/obese individuals with type 2 diabetes.

CONDITIONS

Official Title

Efficacy and Safety of Attapulgite in Patients With Obesity: An Exploratory Clinical Trial

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 60 years, any sex or gender
  • For obese individuals: BMI of 28.0 kg/m2 or higher
  • For overweight or obese individuals with type 2 diabetes: BMI of 24.0 kg/m2 or higher
  • For type 2 diabetes patients: HbA1c between 7.0% and 10.0% or fasting blood glucose between 7.0 mmol/l and 13.3 mmol/l at screening
  • Stable diabetes treatment for 6 months or longer
Not Eligible

You will not qualify if you...

  • Type 1 diabetes, monogenic diabetes, or diabetes caused by pancreatic injury or other secondary causes
  • Severe diabetic complications in the 3 months before the study, such as severe hypoglycemia, diabetic ketoacidosis, or infections
  • Use of products affecting weight in the past 3 months or planned during the study
  • Weight fluctuation greater than 5 kg or 10% in the past 3 months
  • Obesity or overweight caused by endocrine disorders like thyroid problems or Cushing's syndrome
  • Uncontrolled high blood pressure or severe heart, liver, or kidney problems
  • History of gastrointestinal surgery in the past year or other surgeries in the past 6 months, including bariatric surgery
  • Chronic digestive disorders or conditions affecting digestion or absorption
  • Cancer history in the past 5 years or serious immune system disorders
  • Use of probiotics, prebiotics, or antibiotics in the 3 months before enrollment
  • Alcohol abuse or yogurt consumption within 2 weeks before or during the study
  • History of psychiatric or infectious diseases
  • Pregnancy, breastfeeding, or plans for pregnancy during the study
  • Participation in other clinical trials in the past 3 months
  • Any other condition that the investigator feels prevents participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Institute of Metabolism and Endocrinology, Second Xiangya Hospital, Central South University

Changsha, Hunan, China, 410011

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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