Skip to main content
Clinical Trials/NCT06457984
NCT06457984Not yet recruitingNot Applicable

Effects of Selenium Nutritional Supplement of Glucose, Nutritional Status, and Clinical Outcome Among Type 2 Diabetes Patients

Peking Union Medical College Hospital1 site in 1 country300 target enrollmentStarted: June 15, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
300
Locations
1
Primary Endpoint
Drugs of reduce glucose or stop using the antidiabetics.

Study Overview

Brief Summary

According to the prevalence of non-communicable chronic diseases and aging population characteristics, this study is exploring the coexist effects combined with various dimensions: nutritional functions, metabolic homeostasis, inflammation and immunity by the selenium supplementation among type 2 diabetes, which based on insulin resistance, beta-cell function disorders, and body metabolic homeostasis disorders of the mechanism of type 2 diabetes by lifecycle so that could provide with a totally new and safe nutritional method for type 2 diabetes prevention and diagnosis.

Detailed Description

This study will last 16 weeks. There will be 300 subjects enrolled by random lottery methods in this randomized double-blind placebo-controlled clinical study by control group, low dose group and high dose group. During the study processing, follow-up visit by call, questionnaires, blood and stool collection, and functional testing will appear. Statistical analysis would be analysis according to the actual outcome of study.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Masking Description

Double(Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •.Range of age:18~75, both males and females are permitted.
  • •.As to the diagnosis criteria of type 2 diabetes:glucose higher than 13.9mmol/L, drastic fluctuation (upper that 2mmol/L) , severe complication, or coupled with other severe chronic diseases( including overweight, obesity, lipid disorders, hypertension, ASCVD,HF, CKD, never appears.
  • •.Treatments: exercise lifestyle intervention plus oral antidiabetic drugs, such as: single drug(metformin) plus exercise lifestyle intervention, coupled drugs(metformin+acarbose) plus exercise lifestyle intervention, both of them never use insulin.
  • •.Signed with the informed consent, and enrolled in this study in volunteer.

Exclusion Criteria

  • •.Physical fitness must attach to the goal of Par-Q questionnaire and 6 minutes running test. Besides, individuals whose glucose has drastic fluctuation should be excluded.
  • •.Coexist with severe complication and being in the urgent status during the progress of diseases, such as acute complication and infection, hyperplasia retinopathy, severe neuropathy, diabetic foot ulcer, coupled with cardiac insufficiency, diabetic massive proteinuria, recent myocardial infarction, cerebral infarction or cerebral hemorrhage, blood glucose higher than 13.9mmol/L or less than 3.9 mmol/L.
  • •Patients suffering various serious chronic diseases, including unstable angina, uncontrolled arrhythmia, severe valvular heart disease or cardiomyopathy;
  • •Uncontrolled hypertension or blood pressure over 180/110mmHg;
  • •.In the period of trying to conceive or pregnant or lactating.
  • •.Patients who have had cerebral infarction, stroke, history of major surgery, acute attack of infectious diseases or obvious sequelae of infection;
  • •.Sever psychology disorders and mental diseases.
  • •The mass of selenium in body is over the upper limitation, or selenium yeast tablets, as a nutrition supplemented, subjects should not allergic to yeast, and cannot be included. Besides, patients who have recently taken selenium-rich health food or medicine;
  • •Severe malnutrition and overnutrition;
  • •Significant mobility and cognitive impairment;
  • •.Sickle cell disease, hemodialysis, recent blood loss or blood transfusion, etc.

Arms & Interventions

Low dose selenium supplementation group+lifestyle intervention

Experimental

Low dose selenium supplementation:50μg/d +lifestyle intervention

Intervention: Selenium nutritional supplementation (Dietary Supplement)

High dose selenium supplementation group+lifestyle intervention

Experimental

High dose selenium supplementation :300μg/d+lifestyle intervention

Intervention: Selenium nutritional supplementation (Dietary Supplement)

Placebo control group+lifestyle intervention

Placebo Comparator

Placebo control group: sugar free chunk gum 1piles/d+lifestyle intervention

Intervention: Selenium nutritional supplementation (Dietary Supplement)

Outcomes

Primary Outcomes

Drugs of reduce glucose or stop using the antidiabetics.

Time Frame: 12 weeks

Dose or types of antidiabetics drugs would reduce.

Secondary Outcomes

  • GPX activity(12 weeks)
  • Situation of glucose(12 weeks)
  • Status of immunity(12 weeks)
  • Nutrition status of selenium(12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yu Kang, MD

Professor

Peking Union Medical College Hospital

Study Sites (1)

Loading locations...

Similar Trials