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This hydrogel refers to the specific control arm treatment used in a Phase 2 randomized, double-blind clinical trial led by Carlos E. Salas for chronic neuropathic diabetic foot ulcers. The formulation is described as a moisture-retentive wound dressing containing water, carboxymethyl cellulose, and sodium alginate, or alternatively as a standard hydrogel containing collagen, panthenol, and allantoin. It is designed to maintain a moist wound environment and promote autolytic debridement, serving as the active comparator against the proteolytic fraction P1G10 derived from *Vasconcellea cundinamarcensis*.
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