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Development and feasibility of randomized trial to reduce urinary bisphenols in women with obesity.

Todd Alan HagobianZoe Delli-BoviAdrian MercadoAlyssa BirdMegan GuySuzanne Phelan
Published in: Pilot and feasibility studies (2021)
In women with obesity, the 3-week intervention was considered feasible with promising preliminary results of decreasing BPS concentrations. These data warrant future large-scale clinical trial interventions to reduce bisphenol exposure and determine whether reductions in bisphenols positively impact diabetes and cardiovascular disease risk markers. This study was retroactively registered at ClinicalTrial.gov Identifier NCT03440307.
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