An open-label, single Center, observational Clinical evaluation stUdy to assess the accuracy of a WearAble device for viTal sign monitoring as Compared to tHe conventIonal digItal devices - ACCUWATCH-II

GOQii Technologies Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新: 2022年10月17日

试验速览

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•1. Participants willing to sign an Informed Consent Form indicating that they understand the purpose of and the procedures required for the study and are willing to participate in it.
•2. Male and female patients visiting the out-patient department of the hospital who are of age 18 years and above.
•3. Patient having cardiac comorbidity will be considered for enrolment.

•1. Patients who are on ventilator or other life support systems.
•2. Patients who have taken any food, drug or other exposed other factors which will influence the blood pressure levels
•3. Patients who are allergic to the wearable wrist band materials.
•4. Participation in another clinical study concurrently.
•5. Any other specific reason which inhibits active participation of the patient in the study as determined by the Investigator.

发起方

GOQii Technologies Pvt Ltd