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Effect of using sweetener sucralose for 12 weeks on body weight, glycemic and lipid parameters among adults with diabetes in India

Effect of low- calorie sweetener - Sucralose (Sugar Free Natura) on cardio metabolic risk factors and Gut Microbiome among obese and adults with diabetes in India- A randomized trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032686
Enrollment
210
Registered
2021-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: LCS- sucralose (pellet/powder/liquid form): Participants will be advised to use LCS-Sucralose (in either pellet or powder or liquid form) in place of sugars in tea/coffee/ beverages for

Sponsors

Madras Diabetes Research Foundation
Lead Sponsor

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

MeasureTime frame
Assessing the change in HbA1c with LCS- sucralose (pellet/powder/liquid form)Timepoint: 12 weeks

Secondary

MeasureTime 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

Public ContactMrs Sudha Vasudevan

Madras Diabetes Research Foundation

s2r_7@mdrf.in04443968487

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 9, 2026