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NCT Number: NCT06813170

Diet With or Without Metarecod® in Obese Subjects With Type 2 Diabetes

Obesity is considered the largest chronic non-communicable disease (globesity) worldwide with a growing trend in the near future. Weight loss programs are strongly recommended in obese patients, especially with type 1 diabetes mellitus (T2DM), although the majority of subjects do not reach or maintain the recommended weight loss target with nutritional intervention alone and one-third of those who achieve a significant weight loss returns to original body weight within one year. Metarecod® (Neopolicaptil Gel Retard) is a substance based medical device consisting of a macromolecule complex derived from high-fiber raw materials, whose mode of action consists in creating an endoluminal gel in the gut that limits glucose and lipids absorption. The primary aim of the present study is to assess whether the combination of Metarecod® and standard diet as compared to diet alone can achieve a superior weight loss over 12 months of treatment. The present study will also compare the effects of the combination of Metarecod® and diet vs diet alone on:

1. the improvement of glycemic variability and metabolic indexes; 2. the oxidative status, the endothelial anti-thrombotic activity, the inflammatory status; 3. the induction of favorable changes in gut microbiota composition and intestinal permeability.

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Key information

Age range

30 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fondazione Policlinico Universitario A. Gemelli IRCCS; UOC Diabetologia

Rome, Lazio, 00168, Italy

Location contact

Dario Pitocco

PRINCIPAL_INVESTIGATOR

Dario Pitocco, Prof

CONTACT

[email protected]

+390630155701

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed Informed consent at study entry;
  • Age: 30-70 years;
  • T2DM diagnosis according to the American Diabetes Association criteria since ≥6 months;
  • Stable metabolic control as indicated by levels of glycated hemoglobin (HbA1c) <7.5% on two consecutive measurements before study enrollment;
  • Body mass index (BMI) level ≥30 Kg/m2 during the 3 months preceding randomization.

Exclusion criteria

  • Chronic treatment with corticosteroids and/or chronic treatment with non-steroidal inflammatory drugs, defined as ≥3 times/week with the rationale that these drugs independently impact on the whole inflammatory state;
  • Clear indication for dual antiplatelet therapy and/or anticoagulant therapy (full dose);
  • Active cancer or cancer in complete remission from less than one year, except for treated early-stage squamous or basal cell skin carcinomas;
  • For women with childbearing potential, pregnancy.

Treatment and study plan

Metarecod

Dietary Supplement

Policaptil Gel Retard: Metarecod®. The medical device will be given as 1 sachet twice daily

Diet

Other

Diet program will be planned to achieve a ≥8% body weight relative reduction over 12 months and tailored calculating a 20% caloric relative decrease from habitual energy intake, corresponding to an average energy deficit of approximately 500 kcal/daily (approximately a total of 1,200-1,500/daily Kcal for women and 1,500-1,800/daily Kcal for men), with <30% of total calories from fat (<10% from satured fats) and at least 15% of total calories from proteins. For carbohydrate intake, low glycemic index food will be preferred to high glycemic index food, to prevent higher post prandial glycemic excursions

Primary outcomes

  1. Body Weight

    Time frame: 12 months

    Difference in body weight expressed in kg after 12 months between randomized arms

Secondary outcomes

  1. Glycemic variability

    Time frame: 12 months

    Glycemic variability, as assessed by continuous glucose monitoring (CGM)

  2. 8-iso-Prostaglandin (PG) F2α

    Time frame: 12 months

    Change on the oxidative status in vivo, as assessed by the measurement of the urinary excretion of the F2-isoprostane

  3. 2,3-dinor-6-keto-PGF1α

    Time frame: 12 months

    Change of the endothelial anti-thrombotic activity in vivo as assessed by the production of the vasodilator and platelet inhibitor prostanoid, prostacyclin (PGI2), major urinary enzymatic metabolite 2,3-dinor-6-keto-PGF1α

  4. Interleukin (IL)-6

    Time frame: 12 months

    Change on inflammatory status assessed through the change of serum levels of interleukin (IL-6)

  5. C-reactive protein

    Time frame: 12 months

    Change on inflammatory status assessed through the change of serum levels of C-reactive protein (CRP)

  6. Waist circumference

    Time frame: 12 months

    Change in waist circumference after 12 months between arms

  7. Achieving the target weight loss

    Time frame: 12 months

    Percentage of subjects who will reach the target percentage weight loss of 8%

  8. Gut microbiota composition

    Time frame: 12 months

    Gut microbiota composition, assessed by 16S RNA sequencing

Study contacts

Contact information is provided by the study sponsor or research team.

Dario Pitocco

CONTACT

[email protected]

+39 0630154071

Sponsors and collaborators

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Other

Registry information

Official study title

Diet With or Without Metarecod® in Obese Subjects With Type 2 Diabetes: Effect on Body Weight, in Vivo Oxidative Stress, Endothelial Function, Low-grade Inflammation and Gut Microbiota

Acronym: MONDO

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Feb 6, 2025
Registry last updated
Feb 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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