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Completed

NCT Number: NCT07713576

Clinical Trial of Wrist Ambulatory Blood Pressure Monitor in Conformance With the ISO 81060-2:2018+AMD1:2020+AMD2:2024.

The accuracy and safety of the Wrist Ambulatory Blood Pressure Monitor (Model: RIV-B10) were assessed according to the requirements of ISO 81060-2:2018+AMD1:2020+AMD2:2024.

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Key information

Conditions

Blood Pressure

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Chenzhou First People's Hospital

Chenzhou, Hunan, 423000, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Voluntarily participate in this clinical trial and sign informed consent;
  • Subjects must be willing and able to comply with the study steps;
  • Subjects aged 18 and above with wrist circumferences of 13.0-21.0 cm.

Exclusion criteria

  • Subjects whose ECG during the screening period showed severe arrhythmias (atrial fibrillation, atrial flutter, ventricular flutter, ventricular fibrillation, ventricular tachycardia, junctional tachycardia, sinus arrest, pathological sinoatrial node syndrome, pacemaker rhythm);
  • Subjects with sickle cell disease;
  • Subjects who have undergone previous mastectomy or arm lymph node resection;
  • Subjects allergic to nylon, fluor rubber, or hydrogenated nitrile rubber (HNBR);
  • Subjects with wounds on the limbs at the measurement site or inflammation in the wrist;
  • Subjects undergoing intravenous infusion, blood transfusion, or other catheter insertion at the measurement site of the limb;
  • Those who ate, drank alcohol, smoked, or exercised vigorously within 30 minutes prior to the study;
  • Subjects who have participated in other clinical investigations that may affect this trial within the past 30 days;
  • Investigator believe that subjects should not participate in this clinical trial.

Treatment and study plan

Wrist Ambulatory Blood Pressure Monitor/mercury sphygmomanometer

Device

Wrist Ambulatory Blood Pressure Monitor Comparing blood pressure measured by wrist blood pressure monitor with mercury sphygmomanometer .

Primary outcomes

  1. Blood pressure mean deviation and standard deviation- evaluation criterion 1

    Time frame: 30 minutes

    The mean deviation and standard deviation between the blood pressure values measured by the investigational deviceand those obtained using the auscultatory method with the reference device. This calculation is performed on valid data pairsof subjects (n≥255).

    Evaluation criterion 1: The blood pressure mean deviation should not exceed ±5mmHg, and the standard deviation should not exceed 8mmHg.

  2. Blood pressure mean deviation and standard deviation- evaluation criterion 2

    Time frame: 30 minutes

    The mean deviation and standard deviation between the blood pressure values measured by the investigational device and those obtained using the auscultatory method with the reference device. This calculation is performed on the valid data group of all subjects (m≥85).

    Evaluation criterion 2: The blood pressure standard deviation within the valid data group (m ≥ 85) should not exceedthe maximum allowable standard deviation corresponding to the mean deviation listed in Criterion 2 in section 5.2.4.1.2 b of ISO 81060-2:2018+AMD1:2020+AMD2:2024.

  3. The mean deviation and standard deviation of blood pressure measurements under ambulatory blood pressure monitoring

    Time frame: 30 minutes

    The mean deviation and standard deviation of the blood pressure within the valid data group are calculated to evaluate whether the clinical accuracy of the investigational device meets the requirements outlined in ISO 81060-2:2018+AMD1:2020+AMD2:2024 , specifically in section 5.2.4.1.2a).

    The blood pressure mean deviation should not exceed ±5mmHg, and the standard deviation should not exceed 8mmHg.

  4. The mean deviation and standard deviation of blood pressure measurements under exercise stress condition

    Time frame: 30 minutes

    The mean deviation and standard deviation of the blood pressure within the valid data group are calculated to evaluate whether the clinical accuracy of the investigational device meets the requirements outlined in ISO 81060-2:2018+AMD1:2020+AMD2:2024, specifically in section 5.2.4.1.2a).

    The blood pressure mean deviation should not exceed ±5mmHg, and the standard deviation should not exceed 8mmHg.

Sponsors and collaborators

Lead sponsor

Huawei Device Co., Ltd

Industry

Registry information

Official study title

Clinical Trial on the Effectiveness and Safety of Blood Pressure Function System of Wrist Ambulatory Blood Pressure Monitor

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 20, 2026
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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