A study on the effect of bitter gourd (Momordica charantia) containing food on blood glucose level in human.

Phase 1

• Conditions: high normal blood glucose and borderline hyperglycemia

• Registration Number: JPRN-UMIN000015207
• Lead Sponsor: Suntory Global Innovation Center Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-10-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

Not provided

Exclusion Criteria

(1)Subjects who take continuous medical treatment. (2)Subjects who constantly use supplements and/or functional foods (including Food for Specified Health Uses) affecting the test results. (3)Subjects who have contracted or are contracting heart disease, liver disease, kidney disease and digestive disease. (4)Subjects who are pregnant or have possibility to bocome pregnant or planning to become pregnant during the study or breast-feeding woman. (5)Subjects who drink alcohol a lot (6)Subjects who have an extremely irregular diet habit or alternative work schedule or work on midnight shift (7)Subjects who have allergic reaction to drug medicine and food. (8)Subjects who have systolic blood pressure less than 90 mmHg. (9)Subjects who donated 200 mL of blood and/or blood components within the last one month prior to the current study. (10)Male subjects who donated 400 mL of blood within the last three months prior to the current study. (11)Female subjects who donated 400 mL of blood within the last four months prior to the current study. (12)Male subjects whose blood was collected more than 1200 mL within the last twelve months when the amount of blood sampling in the current study is added. (13)Female subjects whose blood was collected more than 800 mL within the last twelve months when the amount of blood sampling in the current study is added. (14)Subjects who are participating in other clinical studies for drug medicine or food, or who finished clinical study within four weeks, or who are planning to participate in other clinical study. (15)Subjects who are judged as unsuitable for the study by the principal investigator for other reasons.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Area under the curve of blood glucose level after ingestion of rice

Secondary Outcome Measures

Name	Time	Method
Blood glucose level at each blood sampling time after ingestion of rice