Browse through all publications from the Institute of Global Health Innovation, which our Patient Safety Research Collaboration is part of. This feed includes reports and research papers from our Centre. 

Citation

BibTex format

@article{Byrne:2026:10.1002/oby.70066,
author = {Byrne, JP and Hinton, EC and Humayun, AM and Pournaras, DJ and Elsworth, RL and Brunstrom, JM and Hamilton-Shield, JP and Sumeray, M and Easter, C and Ashrafian, H},
doi = {10.1002/oby.70066},
journal = {Obesity (Silver Spring)},
pages = {88--100},
title = {A Randomized, Double-Blind, Placebo-Controlled Pilot Trial With Open-Label Extension of Sirona, a Hydrogel for Weight Loss.},
url = {http://dx.doi.org/10.1002/oby.70066},
volume = {34},
year = {2026}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - OBJECTIVE: This study investigated the safety, tolerability, and preliminary efficacy of Sirona, a novel gastro-retentive, dual-network polymer for weight management. METHODS: This pilot trial comprised a randomized, parallel-group, double-blind, placebo-controlled (3:1 ratio), 12-week period, with a 12-week open-label extension (OLE), in participants with BMI of 30-40 kg/m2. Primary endpoints were feasibility, tolerability, and safety; secondary endpoints included weight loss and dietary intake, tested using Hedge's g [95% CI] as a measure of effect size. RESULTS: Participants received Sirona (n = 29/38) or Placebo (n = 9/38) (mean [SD] age = 40.9 [8.4]; weight = 101.7 [12.9] kg; BMI = 35.6 [3.0]; 29/38 female and 23/38 White British). Dosing was well tolerated (RCT Sirona: 95.2 [11.0]%; RCT Placebo: 97.8 [3.5]%; RCT + OLE Sirona: 93.1 [13.0]%). No serious adverse events occurred. Of the adverse events, nausea was most prominent (74.8%), mostly graded mild (79.3%) and requiring no intervention (84.4%). Percentage total body weight loss was greater for Sirona compared to Placebo after 12 weeks (3.9 [3.0]% versus 1.0 [2.1]%, g = 0.96 [-1.81, -0.10]). Weight loss continued in the OLE (change from baseline = 4.4 [3.8]%). Dietary intake reduced from baseline after 12 weeks of treatment (-382.5 [519.3] kcal; Placebo = 93.5 [670.3] kcal, g = -0.8 [-1.7, 0.0]) and after 24 weeks (-338.2 [486.7] kcal, g = 0.7 [0.2, 1.1]). CONCLUSIONS: Sirona was well tolerated, with mild, primarily gastrointestinal side effects. Reduced weight and dietary intake suggest Sirona is suitable as a nonpharmacological treatment for weight management. TRIAL REGISTRATION: ISRCTN14083641 (https://doi.org/10.1186/ISRCTN14083641).
AU - Byrne,JP
AU - Hinton,EC
AU - Humayun,AM
AU - Pournaras,DJ
AU - Elsworth,RL
AU - Brunstrom,JM
AU - Hamilton-Shield,JP
AU - Sumeray,M
AU - Easter,C
AU - Ashrafian,H
DO - 10.1002/oby.70066
EP - 100
PY - 2026///
SP - 88
TI - A Randomized, Double-Blind, Placebo-Controlled Pilot Trial With Open-Label Extension of Sirona, a Hydrogel for Weight Loss.
T2 - Obesity (Silver Spring)
UR - http://dx.doi.org/10.1002/oby.70066
UR - https://www.ncbi.nlm.nih.gov/pubmed/41090617
VL - 34
ER -

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