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ENROLLING BY INVITATION
NCT07494253
NA

Effects of Reducose on Postprandial Glycemic Levels in Obese Children and Adolescents

Sponsor: University of Bari Aldo Moro

View on ClinicalTrials.gov

Summary

The study entitled "Effects of Reducose on Postprandial Glycemic Peak in Obese Children and Adolescents: A Pilot Study" aims to evaluate the improvement in glycemic and insulinemic levels produced by Reducose, a food supplement extracted from white mulberry (Morus alba), after 12 weeks of treatment in a cohort of obese children and adolescents. Clinical and anthropometric data (age, sex, weight, height, BMI, pubertal stage) will be collected, along with data from blood chemistry tests performed during routine follow-up visits, in accordance with Good Clinical Practice guidelines.

Official title: Effects of Reducose on Postprandial Glycemic Levels in Obese Children and Adolescents: A Pilot Study (PEDRED)

Key Details

Gender

All

Age Range

6 Years - 16 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-06-01

Completion Date

2026-06-30

Last Updated

2026-03-27

Healthy Volunteers

No

Conditions

Interventions

DIETARY_SUPPLEMENT

Reducose

Reducose 250 mg oral sticks, administered twice daily, 1 at lunch and 1 at dinner, for 12 weeks

OTHER

Placebo

Participants will receive 2 placebo sticks per day, 1 at lunch and 1 at dinner, for 12 weeks. The placebo sticks will be indistinguishable from the active product and will contain inert excipients.

Locations (1)

Ospedale Pediatrico Giovanni XXIII

Bari, Italy