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NCT04931264

Clinical Trial of YuWell YE660D Blood Pressure Monitor in General Population According to the ISO 81060-2:2018

Completed NA Last updated 10 March 2022
What this trial tests

NA trial testing YuWell YE660D Electronic Sphygmomanometer in Blood Pressure in 92 participants. Completed in 8 March 2022.

Timeline
1 September 2021
Primary endpoint
1 March 2022
8 March 2022

Quick facts

Lead sponsorThe Second Hospital of Nanjing Medical University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment92
Start date1 September 2021
Primary completion1 March 2022
Estimated completion8 March 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

The Second Hospital of Nanjing Medical University

Who can join

12 and older, any sex, with Blood Pressure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the accuracy of the YuWell YE660D oscillometric upper-arm blood pressure monitor for clinic and home in general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Blood Pressure

Currently open trials in the same condition.

Other The Second Hospital of Nanjing Medical University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04931264.

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