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A study on healthy people to see the effect on blood glucose levels after eating a high sugar food with fiber and to see the effect of fiber on hunger.

Not Applicable
Registration Number
CTRI/2015/07/006013
Lead Sponsor
Mr Ajay Nilawar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
32
Inclusion Criteria

1.Males or females in the age 18- 65 years (both inclusive).

2.Be of normal health as determined by the investigator from medical history, clinical and physical examination.

3.Random blood sugar level <= 200 mg/dl at screening.

4.BMI between 18.5 to 27 kg/m2 (both inclusive).

5.Must be willing to or likely to comply with all study requirements.

6.Must be able and willing to provide written informed consent.

7.Women of childbearing potential should have a negative pregnancy test at the time of screening and agree to use contraception during the study.

Exclusion Criteria

1.Previous history of any clinically significant medical condition e.g. cardiovascular, type 2 diabetes mellitus, eating disorder or serious gastrointestinal indications which in opinion of investigator may jeopardize subjectâ??s safety and preclude trial participation.

2.Suffering from any condition which may interfere with nutrient absorption, distribution, metabolism and excretion in opinion of the Investigator e.g. subacute obstruction.

3.Current use of medication which may interfere with the digestion and nutrient absorption or affect glucose tolerance and estimation in opinion of the Investigator.

4.Abuse of drugs or alcohol.

5.Known case of sensitivity to Gluten or Coeliac disease.

6.Pregnant or lactating women.

7.Currently participating or had participated in any other interventional study in last 1 month prior to screening.

8.Patients who are unlikely to comply with protocol requirements (e.g. non-cooperative behavior, illiterate, inability to attend study visits required by the protocol).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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