None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: .Adults with type 2 diabetes and BMI greater than 18.5 .Hba1c 8-12% .Individuals on stable OHA/insulin dose .Willing to follow study protocol .Willing to give informed consent .Willing to use LCS-sucralose for 12 weeks
Exclusion criteria
Exclusion criteria: .Any acute infections like viral fever, typhoid, cold, diarrhea, constipation last 1 month .Individuals with any disorders of liver, kidney, thyroid, or other endocrine diseases or other complications such as respiratory disorders, diabetes, cancer or heart attack and stroke that hinders the intervention .Individuals with any eating disorder .Participants undergoing any treatment or medications including antibiotics .Pregnant and lactating Women .Plans to relocate in the next 3 years. .Planning longer duration of travel out of town
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessing the change in HbA1c with LCS- sucralose (pellet/powder/liquid form)Timepoint: 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessing the effect of LCS-sucralose on body weight Glycemic parameters ,Lipid profile,Inflammatory markers, Advanced glycation end products and Gut microbiome Timepoint: 12 weeks | — |
Countries
India
Contacts
Madras Diabetes Research Foundation