A clinical study to determine the blood glucose response of a dietary fiber on high Glycemic index food and satiety response of a dietary fiber in healthy volunteers.

Mr Ajay Nilawar0 个研究点目标入组 32 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•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.

•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).

发起方

Mr Ajay Nilawar