Completed

WristBPM01Verify Wrist BPM TMB-1117 to Comply With ANSI/AAMI SP10

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Blood pressure Transtek Wrist Blood Pressure Monitor, TMB-1117

+ Blood pressure Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-2

Device
Who is being recruted

Cardiovascular Diseases

+ Vascular Diseases

+ Hypertension

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Interventional
Study Start: May 2012
See protocol details

Summary

Principal SponsorLeo Wang
Last updated: August 13, 2012
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2012

Actual date on which the first participant was enrolled.

Hospital Information Hospital Information The data was collected by Zhongshan City People's Hospital Clinical Investigator Team at Zhongshan City People's Hospital, No.2 Sunwen Dong Road, Zhongshan, Guangdong 528403, P. R. China. Investigator: Dr. Cao Yuedong, Leader; Li Qidong, Nurse A; Chen Wenqian, Nurse B. Contact Dr. Cao Yuedong Tel: +86 760 88823818 Used Equipments DUT (Device Under Test): Transtek Wrist Blood Pressure Monitor, TMB-1117 Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1 mmHg and range: 0-300 mmHg. Test Protocol Test Purpose: The aim of clinical test is to determine, for the purpose of design qualification, the overall performance of the system meeting the following requirement: For systolic and diastolic pressures, treated separately, the mean difference of the paired measurement of the test system and the comparison system shall be ± 5 mmHg or less, with standard deviation of 8 mmHg or less. Target Subject: 1) The subject database shall contain at least 85 subjects. 2) The distribution of blood pressure of the subjects required to be: At least 10 percent below 100 mmHg systolic; at least 10 percent above 160 mmHg systolic; at least 10 percent below 60 mmHg diastolic; at least 10 percent above 100 mmHg diastolic; with the remainder distributed between these outer limits. 3. Identification and precision of equipment used According to ANSI/AAMI SP10, the maximum measurement error of the non-automatic sphygmomanometers used in the comparing test shall not exceed 1.0mmHg at the temperature of the test. The manometer was used to verify its accuracy before test. The clinical study was conducted according to the protocol described in the ANSI/AAMI SP10 with 85 subjects. 4. Test procedures (auscultatory method, same-limb sequential measurement was chosen) Record the age, gender, and circumference of the left wrist of the subject. Let subject seated or supine calmly for five minutes before test. Measure heart rate in one minute by palpation on radial artery, record it. Two observers shall make simultaneous, blinded, blood pressure determination on the subject's left arm. Each nurse will write down the reading on a small piece of paper, make a tick if there is an auscultatory gap and then submit to the recorder. The two readings separately from two observers will be recorded, and if two observers agree that they find an auscultatory gap this time, it will also be recorded. The wrist cuff will be take off, after 90 seconds rest, TMB-1117 cuff will be taken on and tested, and the readings (systolic, diastolic, mean BP and Heart rate) be recorded. For each subject, repeat 3) and 5) to get 3 measurements. Repeat step 1) to 6) for every subject. 5. Note: No motion and speaking are allowed during the measurement. The reference device's cuff release at the rate about 3 mmHg/s so to ensure an accurate reading of observer. The arm, wrist and the haear of subject to keep on the same height when measurement. Test environment: Temperature: 20±1 ℃; Relative humidity: 40~50%.

NCT01662947
Principal SponsorLeo Wang
Last updated: August 13, 2012
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

85 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular DiseasesVascular DiseasesHypertension

Criteria

1 inclusion criteria required to participate
male,female

1 exclusion criteria prevent from participating
below 18 years old

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
DUT: Transtek Wrist Blood Pressure Monitor TMB-1117 Measurement: Blood Pressure Groups/Cohorts: DUT

Group II

Experimental
Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1mmHg and range: 0-300mmHg. Measurement: Blood Pressure Groups/Cohorts: Reference

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Zhongshan City People's Hospital

Zhongshan, ChinaOpen Zhongshan City People's Hospital in Google Maps
CompletedOne Study Center