Trial reportNature communications2026
Totum-63, a plant-based polyphenol-rich extract, in prediabetes or early-stage type 2 diabetes: an international, multicenter, randomized controlled trial.
Trial report in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04423302 (Randomized Placebo-controlled Double-blinded Study of the Effect of TOTUM-63 on Glucose and Lipid Homeostasis in Subjects With Dysglycemia), which is not on this map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Randomized Placebo-controlled Double-blinded Study of the Effect of TOTUM-63 on Glucose and Lipid Homeostasis in Subjects With Dysglycemia
Who cites it
1 citing paper in PubMed.
- Trial
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
16 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This multicenter, parallel-arm, superiority, randomized, double-blind, placebo-controlled study evaluates the efficacy of Totum-63 (T63), a polyphenol-rich blend of plant extracts, in improving fasting plasma glucose (FPG) in individuals with prediabetes or early-stage type 2 diabetes (T2D). Individuals from seven European countries with FPG between 110-220 mg/dL were randomized to receive placebo (PBO, n = 210), T63 (5 g/d) distributed thrice daily (T63 TID, n = 212) or twice daily (T63 BID, open-label arm, n = 214) over six months. Individuals were randomly assigned using a dynamic randomization algorithm, stratified by their glycemic status at baseline (FPG < 126 mg/dL or FPG ≥ 126) and the investigational site country. The primary outcome was the FPG change in T63 TID compared to PBO in the intention-to-treat population. Secondary assessments included changes in diabetes biomarkers, lipid profile, anthropometric measurements and subpopulation analyses based on glycemic status. During the whole study, neither the investigators nor the subjects were aware of the product they tested, except in the open arm. After six months, FPG was significantly reduced in the T63 TID group (PBO-adjusted mixed model estimated difference, PBO-AD = -3.8 mg/dL, 95% CI: [-5.9; -1.7], p = 0.0149) and the T63 BID group (PBO-AD = -5.5 mg/dL, 95% CI: [-9.7; -1.3] p < 0.001). Hence, T63 may represent a non-pharmaceutical strategy for T2D prevention. ClinicalTrials.gov Identifier: NCT04423302. Funding: This trial was funded by Valbiotis®.
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