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Clinical Trials/CTRI/2020/06/025988
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.

Registry
who.int
Start Date
TBD
End Date
July 6, 2020
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
Dr Reddys Laboratories

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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