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Efficacy of a Brown Seaweed Extract Rich in Polyphenols on Glycemic Response to Sucrose in Human

I

innoVactiv

Status and phase

Completed
Phase 1

Conditions

Hyperglycemia

Treatments

Dietary Supplement: Reduction of glycemic index of ingested foods

Study type

Interventional

Funder types

Industry

Identifiers

NCT01384110
2010-RD-01-CLN

Details and patient eligibility

About

The primary endpoint of this trial will be to evaluate if a single administration in human of a lemon ice tea containing 500 mg of a polyphenol-rich algal powder is able to reduce postprandial glycemia and insulinemia.

Enrollment

43 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteer aged 18 to 60
  • BMI between 20 and 30
  • Non-smoking
  • Using valid contraceptive method (women of childbearing age)

Exclusion criteria

  • Iodine allergy, or allergy to components of the test product or placebo or standard meal
  • Diabetes
  • Use of dietary supplements for duration of study
  • History of gastro-intestinal affections, anemia, major surgeries or surgeries of the stomach or digestive tract

Trial design

43 participants in 2 patient groups, including a placebo group

Brown Seaweed Lemon Tea
Experimental group
Description:
Single administration of lemon tea containing 500 mg of brown seaweed powder and 50 g of sucrose
Treatment:
Dietary Supplement: Reduction of glycemic index of ingested foods
Placebo lemon tea
Placebo Comparator group
Description:
Single administration of placebo lemon tea containing 50 g of sucrose
Treatment:
Dietary Supplement: Reduction of glycemic index of ingested foods

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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