CTRI/2020/06/025988
Completed
未知
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 sites50 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: R688- Other general symptoms and signs
- Sponsor
- Dr Reddys Laboratories
- Enrollment
- 50
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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