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Table 2 Exclusion criteria

From: Postbariatric EArly discharge Controlled by Healthdot (PEACH) trial: study protocol for a preference-based randomized trial

Patients of psychiatric wards, inmates or prisons, or other state institutions

Investigator or any other team member involved directly or indirectly in the conduct of the clinical study

Any skin condition, for example, prior rash, discoloration, scars, or open wounds at the area where the Healthdot needs to be placed

Known allergy for the tissue adhesive used in the Healthdot (white band-aid)

Use of topical that is known to influence the skin at the test area (such as medical and non-medical creams or lotions)

Patient with active implantables such as Implantable Cardioverter Defibrillator (ICD) and pacemaker

Left lower rib (place where Healthdot will be applied) is involved in the area of surgery, area of disinfection, or area where bandages are needed.

Expected participation less than 8 days