Trials / Recruiting
RecruitingNCT06457568
Validation Study of CONTEC08C Electronic Sphygmomanometer
Validation of the CONTEC08C Oscillometric Blood Pressure Monitor in General Population According to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018)
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- Chinese Academy of Medical Sciences, Fuwai Hospital · Academic / Other
- Sex
- All
- Age
- 12 Years – 79 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to assess the accuracy of the CONTEC08C automated oscillometric upper-arm sphygmomanometer in the general population for clinical use 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).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Blood pressure measurement | The blood pressure measurement was taken simultaneously by two observers using mercury sphygmomanometer and by a supervisor using the tested device, CONTEC08C. |
Timeline
- Start date
- 2024-05-25
- Primary completion
- 2024-07-25
- Completion
- 2024-08-01
- First posted
- 2024-06-13
- Last updated
- 2024-06-24
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06457568. Inclusion in this directory is not an endorsement.