Clinical Study of Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10 (BPM_S)
Primary Purpose
Hypertension
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Comparison Test to Yuyue Medical BP Meter, YYBP-212
Sponsored by

About this trial
This is an interventional diagnostic trial for Hypertension focused on measuring blood pressure, heart rate
Eligibility Criteria
Inclusion Criteria:
- male,female,
Exclusion Criteria:
- below 18 years old
Sites / Locations
- Zhongshan City People's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Blood Pressure, Heart Rate, Monitor
Arm Description
Device Comparison Test DUT: Transtek Blood Pressure Monitor, LS-802 Refrence Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1mmHg and range: 0-300mmHg. Groups/Cohorts: Blood Pressure & Heart Rate Monitor
Outcomes
Primary Outcome Measures
Verify the accuracy of measure functions of device
Verify the accuracy of device if meet the requirements of ANSI/AAMI SP10 when it measure Systolic & Diastolic blood pressure.
Secondary Outcome Measures
Full Information
NCT ID
NCT01502553
First Posted
December 21, 2011
Last Updated
December 29, 2011
Sponsor
Leo Wang
Collaborators
BTS International
1. Study Identification
Unique Protocol Identification Number
NCT01502553
Brief Title
Clinical Study of Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10
Acronym
BPM_S
Official Title
Verify the Functions of BPM LS-802 to Comply With ANSI/AAMI SP10
Study Type
Interventional
2. Study Status
Record Verification Date
December 2011
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
November 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Leo Wang
Collaborators
BTS International
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The clinical protocol of the clinical testing of this device:
Objective of the test: To verify the function of device.
Test methods and procedures: Performance test in two positions: Seated and Supine.
DUT: Transtek Blood Pressure Monitor, Model: LS-802. Cuff size: 22-32 cm and 22-42 cm.
Comparison device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1 mmHg and range: 0-300 mmHg.
Study endpoints: Comply with ANSI/AAMI SP10-2002 standard.
Statistical methodology used: Description of statistical methods.
Result: Meet the requirements of SP10.
Detailed Description
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 Blood Pressure Monitor, Model: LS-802. Cuff size: 22-32 cm and 22-42 cm.
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 95 subjects.
4. Test procedures (auscultatory method, same-limb sequential measurement was chosen)
Record the age, gender, and circumference of the left arm of the subject.
Let subject seated or supine calmly for two minutes before test.
Measure heart rate in one minute by palpation on radial artery, record it.
As shown in Fig. 0, 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 arm cuff will be take off, after 90 seconds rest, TMB-986 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:
1) No motion and speaking are allowed during the measurement. 2) DUT uses the 22-42 cm Cuff when the arm circumference of patients above 32 cm and the other patients use 22-32 cm Cuff.
3) The reference device's cuff release at the rate about 3 mmHg/s so to ensure an accurate reading of observer.
4) The arm of the same height and heart when measurement. 5) Test environment: Temperature: 20±1 ℃; Relative humidity: 40~50%.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
blood pressure, heart rate
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
95 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Blood Pressure, Heart Rate, Monitor
Arm Type
Experimental
Arm Description
Device Comparison Test DUT: Transtek Blood Pressure Monitor, LS-802 Refrence Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1mmHg and range: 0-300mmHg.
Groups/Cohorts: Blood Pressure & Heart Rate Monitor
Intervention Type
Device
Intervention Name(s)
Comparison Test to Yuyue Medical BP Meter, YYBP-212
Other Intervention Name(s)
Brand names: Yuyue, Serial numbers: YYBP20100013437, Code name: YYBP-212
Intervention Description
DUT: Transtek Blood Pressure Monitor, LS-802. Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1mmHg and range: 0-300mmHg.
Primary Outcome Measure Information:
Title
Verify the accuracy of measure functions of device
Description
Verify the accuracy of device if meet the requirements of ANSI/AAMI SP10 when it measure Systolic & Diastolic blood pressure.
Time Frame
10 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
male,female,
Exclusion Criteria:
below 18 years old
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuedong Cao, Doctor
Organizational Affiliation
Zhongshan People's Hospital, Guangdong, China
Official's Role
Study Director
Facility Information:
Facility Name
Zhongshan City People's Hospital
City
Zhongshan
State/Province
Guangdong
ZIP/Postal Code
528403
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
20559140
Citation
Alpert BS. Validation of the Tiba Medical Ambulo 2400 ambulatory blood pressure monitor to the ISO Standard and BHS protocol. Blood Press Monit. 2010 Oct;15(5):275-7. doi: 10.1097/MBP.0b013e32833c8b39.
Results Reference
background
Links:
URL
http://www.zsph.com
Description
Related Info
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Clinical Study of Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10
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