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)

Dr Reddys Laboratories0 个研究点目标入组 50 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•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 age18 years and above.

•1) Patients who are on ventilator or other life support systems.
•2) Patients who are allergic to the wearable wrist band materials.
•3) Participation in another clinical study concurrently.
•4) Any other specific reason which inhibits active participation of the patient in the study as determined by the Investigator.

发起方

Dr Reddys Laboratories