Clinical Study to Evaluate the Efficacy of Collagen Peptide as an Add-on Nutritional Therapy in the Management of Diabetes Mellitus (Type II) in Adult Subjects.

Not Applicable

Completed

• Conditions: Health Condition 1: E119- Type 2 diabetes mellitus without complications

• Registration Number: CTRI/2015/02/005518
• Lead Sponsor: itta Gelatin India Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2016-01-25
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

1.Male and female adults between the ages of 21 and 50 years (both ages inclusive).

2.Subjects with known history of diabetes mellitus (type II).

3.Subjects who are on oral hypoglycaemic agents for control of diabetes mellitus (type II).

4.Subjects who have no known history or diagnosis of complications association with diabetes mellitus (type II).

5.Subjects who are non-alcoholic and non-smokers/non-users of tobacco.

6.Subjects with Body Mass Index between 18 to 32 kg/m2 , both values inclusive.

7.Subjects with clinically normal presentations during physical examination and laboratory investigations â?? complete blood count and serum biochemistry.

Exclusion Criteria

1.Subjects who are vegetarians or vegans or those who object to consumption of animal origin products.

2.Subjects on herbal, ayurvedic, homeopathic medications for the control of diabetes mellitus.

3.Subjects with known history of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, or genitourinary abnormalities or diseases.

4.Subjects who have undergone major surgical procedure 4 weeks prior to randomisation.

5.Subjects who are on steroids, hormone therapy, anti-depressants and anti-psychotics.

6.Subjects who have modified their dosage of primary therapy within one month prior to randomisation.

7.Subjects who are mentally unable to comprehend the responsibilities and adhere to the stipulations of the protocol.

8.Subjects who are known/reported to be pregnant, lactating, planning a pregnancy or unwilling to practice double barrier contraceptive method.

9.Subjects who in the opinion of the investigator are deemed unfit to participate in the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified