Clinical Trial for Liquid Food (Inslow)

Sponsor
Shanghai Meiji Health Science and Technology Co., Ltd. (Industry)
Overall Status
Completed
CT.gov ID
NCT02641743
Collaborator
(none)
36
2
13

Study Details

Study Description

Brief Summary

A carbohydrate adjusted liquid formula (Inslow) using palatinose as the major carbohydrate (>50%) was devised. Consumption Inslow for a long term (3-5 months) is reported to improve glycemic control by reducing the postprandial plasma glucose levels in diabetes and impaired glucose-tolerant subjects (IGT). The present study intends to understand the mechanism on postprandial glycemic responses.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Inslow
  • Dietary Supplement: standard balanced formula
N/A

Detailed Description

The test enteral nutrition formula (Inslow) and the standard balanced formula (Meibalance) were administered in a randomized crossover design to 11 healthy people, 13 IGT and 12 type-2 diabetes, judged by the postprandial state after in taking the two test meals in a random order with a washout period of one week. On the day prior to the test day, subjects were asked to stay at the same facility and to take the same supper with 450 kcal controlled, after 21:00 with only water allowed as ad libitum and not do any exercise. Each participant was taken a fasting blood sample, and then requested to consume one of is energetic test meals (200 kcal per serving) Inslow or standard balanced formula at 7:00 AM. Subsequent blood samples were collected at 30,60,90,and 120 min after meal consumption. The plasma concentrations of glucose, insulin, and free fatty acids were measured for each blood sample. Plasma glucose was measured by hexokinase method, plasma insulin by serum radioimmunoassay method and plasma free fatty acid by enzyme chemical method.Routine blood test and biochemical test were performed using the same blood sample only at fasting stage,including RBC, WBC, TP, ALP, T-Cho, etc., to confirm the status of each subject. Collected blood was applied to analyses at Shanghai Meizhong Clinical Measurement Centre. The enteral nutrition meal Inslow was designed by palatinose, dextrin and fiber as carbohydrate for 56%,23% and 15%, respectively. The standard balanced meal was included dextrin as the main carbohydrate for 85%, together with sugar and fiber.

Study Design

Study Type:
Interventional
Actual Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Increased Insulinogenic Indexes Following Liquid Food (Inslow) Intake in Impaired Glucose Tolerance and Type-2 Diabetic Subjects.
Study Start Date :
Jan 1, 2009
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Feb 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Inslow

Each participant was requested to consume one of is energetic test meals (200 kcal per serving 200ml) Inslow at 7:00 AM.

Dietary Supplement: Inslow
carbohydrate adjusted liquid food using palatinose as the major carbohydrate (>50%)

Placebo Comparator: standard balanced formula

Each participant was requested to consume one of is energetic test meals (200 kcal per serving 200ml) standard balanced formula at 7:00 AM.

Dietary Supplement: standard balanced formula

Outcome Measures

Primary Outcome Measures

  1. plasma glucose concentration [2 weeks]

Secondary Outcome Measures

  1. plasma insulin concentration [2 weeks]

  2. plasma free fatty acid concentration [2 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
52 Years to 61 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Type 2 diabetes (symptoms of diabetes plus fasting plasma glucose level higher than 7.0 mmol/L and glucose levels after 75g oral glucose tolerance test (OGTT) or casual blood glucose level higher than 11.1mmol/L) and IGT patients (glucose levels after 75g OGTT between 7.8 and 11.1mmol/L).
Exclusion Criteria:
  • These patients or subjects have no infectious diseases and were not using any drug.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Shanghai Meiji Health Science and Technology Co., Ltd.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shanghai Meiji Health Science and Technology Co., Ltd.
ClinicalTrials.gov Identifier:
NCT02641743
Other Study ID Numbers:
  • 0001
First Posted:
Dec 29, 2015
Last Update Posted:
Dec 29, 2015
Last Verified:
Dec 1, 2015
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No

Study Results

No Results Posted as of Dec 29, 2015