Ice Plant (Mesembryanthemum Crystallinum) Extract in Patients With Impaired Fasting Glucose

Impaired Fasting Glucose Clinical Trial

Official title:

Evaluation of Efficacy and Safety of Ice Plant (Mesembryanthemum Crystallinum) Extract in Patients With Impaired Fasting Glucose: a Double-blind, Randomized, Placebo-controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05544825
• Other study ID #: 02-2022-016
• Status: Completed
• Phase: N/A
• Start date: July 1, 2022
• Est. completion date: October 31, 2023

Study information

• Verified date: January 2024
• Source: Pusan National University Yangsan Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators will conduct a randomized, double-blind, placebo-controlled study to investigate the effects and tolerability of ice plant (Mesembryanthemum crystallinum) extract in patients with impaired fasting glucose for 12 weeks.

Description:

A previous animal study has indicated that ice plant (Mesembryanthemum crystallinum) extract (IPE) has a substantial effect on attenuating hyperglycemia and modulating gut microbiota composition in diabetic rats. Therefore, IPE might be a promising functional food for the prevention of diabetes. Therefore, the investigators will conduct a randomized, double-blind, placebo-controlled study to investigate the effects of IPE in patients with impaired fasting glucose for 12 weeks; the safety of the compound is also evaluated. The Investigators examine 75-g oral glucose tolerance test (OGTT) (120 minute glucose), 75-g OGTT incremental Area Under the Curve 0-120min, 75-g OGTT (0, 30, 60, 90 minute glucose), fasting insulin, Homeostasis Model Assessment for Insulin Resistance, Quantitative Insulin Sensitivity Check Index, HbA1c, lipid profile (total cholesterol, triglyceride, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol) at baseline and after 12 weeks of intervention. One hundred adults were administered either 2,000 mg of IPE or a placebo each day for 12 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: October 31, 2023
• Est. primary completion date: October 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years to 85 Years

Eligibility

Inclusion Criteria:

• Those with fasting blood glucose of 100 mg/dL or more and less than 140 mg/dL

Exclusion Criteria:

• Those who have been diagnosed with type 1 or type 2 diabetes
• Those who have continuously taken drugs that may affect blood glucose, such as blood glucose-lowering drugs or anti-obesity drugs, within 3 months
• A person who has continuously taken health functional food that can affect blood glucose within 1 month or health functional food can affect the interpretation of the results of this study
• Those who took systemic steroids within 1 month
• Those who lost 0% or more in weight within the last 3 months
• Severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.) within the last 6 months), heart disease (angina pectoris, myocardial infarction, heart failure, arrhythmia that needs to be treated), or a malignant tumor (however, subjects with a history of cerebrovascular disease or heart disease but clinically stable are not eligible for the study at the discretion of the investigator.
• Persons with local or systemic inflammatory diseases
• Persons with renal disease such as hereditary hyperlipidemia, acute/chronic renal failure, nephrotic syndrome
• Persons with systolic blood pressure (BP) 160mmHg or diastolic BP 100mmHg or higher (provided that, those who are stably controlling their BP through drug treatment can participate)
• Those with HbAc1 of 7.0% or higher
• Abnormal liver or renal function (more than twice the normal upper limit of the research institute)
• Those who are currently being treated for thyroid disease
• Those who have a history of gastrointestinal disease (eg, Crohn's disease) or gastrointestinal surgery (except simple appendectomy or hernia surgery) that may affect the absorption of the test food
• Those who have participated or plan to participate in other drug clinical trials within the last 1 month
• Persons taking drugs for psychiatric disorders (except for cases of intermittent medication due to sleep disturbance)
• Persons with alcoholism, drug abuse, or dependence
• Pregnant or lactating or during this human application test period Women who plan to become pregnant during pregnancy
• Those who have a clinically significant history or allergic reaction to drugs or food for human application
• Appropriate methods of contraception among women of childbearing age (condoms, diaphragms, intrauterine contraceptives, male partner Women who do not accept the procedure (if they have undergone resection) (however, women who have undergone sterilization are excluded)

Related Conditions & MeSH terms

• Impaired Fasting Glucose
• Prediabetic State

Intervention

Dietary Supplement:
• Ice plant group
Ice plant extract 2,000 mg/day for 12 weeks
• Placebo group
Placebo 2,000 mg/day for 12 weeks

Locations

Country	Name	City	State
Korea, Republic of	Pusan National University Yangsan Hospital	Yangsan	Gyeungsangnam-do

Sponsors (1)

Lead Sponsor	Collaborator
Pusan National University Yangsan Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	75-g Oral Glucose Tolerance Test (120 minute glucose)	mg/dL	12 weeks
Secondary	Incremental Area Under the Curve 0-120 minutes	mg/dL	12 weeks
Secondary	75-g Oral Glucose Tolerance Test (0, 30, 60, 90 minute glucose)	mg/dL	12 weeks
Secondary	Fasting Insulin	µU/ml	12 weeks
Secondary	Homeostasis Model Assessment for Insulin Resistance	fasting insulin (µU/ml) + fasting glucose (mg/dl)/405	12 weeks
Secondary	Quantitative Insulin Sensitivity Check Index	1/(log(fasting insulin µU/ml) + log(fasting glucose mg/dl))	12 weeks
Secondary	HbA1c	percentage	12 weeks
Secondary	Total cholesterol	mg/dL	12 weeks
Secondary	Triglyceride	mg/dL	12 weeks
Secondary	Low-density lipoprotein cholesterol	mg/dL	12 weeks
Secondary	High-density lipoprotein cholesterol	mg/dL	12 weeks