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Clinical Study of Wrist Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10 Standard (WristBPM01)

Primary Purpose

Efficacy of Wrist BPM Measurement, Hypertension

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Blood pressure Transtek Wrist Blood Pressure Monitor, TMB-1117
Blood pressure Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-2
Sponsored by
Leo Wang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Efficacy of Wrist BPM Measurement focused on measuring blood pressure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • male,female,

Exclusion Criteria:

  • below 18 years old

Sites / Locations

  • Zhongshan City People's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

DUT Arm

Reference Arm

Arm Description

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

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

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

First Posted
August 1, 2012
Last Updated
August 8, 2012
Sponsor
Leo Wang
Collaborators
BTS International
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1. Study Identification

Unique Protocol Identification Number
NCT01662947
Brief Title
Clinical Study of Wrist Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10 Standard
Acronym
WristBPM01
Official Title
Verify Wrist BPM TMB-1117 to Comply With ANSI/AAMI SP10
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2012 (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 efficiency of device. Test methods and procedures: Clinical test in two positions: Seated and Supine. DUT: Transtek Wrist Blood Pressure Monitor, Model: TMB-1117. Cuff size: 13.5 - 21.5 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 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%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Efficacy of Wrist BPM Measurement, Hypertension
Keywords
blood pressure

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
85 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DUT Arm
Arm Type
Experimental
Arm Description
DUT: Transtek Wrist Blood Pressure Monitor TMB-1117 Measurement: Blood Pressure Groups/Cohorts: DUT
Arm Title
Reference Arm
Arm Type
Experimental
Arm Description
Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-212, accuracy: ±1mmHg and range: 0-300mmHg. Measurement: Blood Pressure Groups/Cohorts: Reference
Intervention Type
Device
Intervention Name(s)
Blood pressure Transtek Wrist Blood Pressure Monitor, TMB-1117
Other Intervention Name(s)
DUT TMB-1117 measurement
Intervention Description
Systolic, Diastolic pressure.
Intervention Type
Device
Intervention Name(s)
Blood pressure Reference Device: Yuyue Medical Blood Pressure Meter, YYBP-2
Other Intervention Name(s)
Reference mercury sphygmomanometer measurement
Intervention Description
Systolic, Diastolic pressure
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
Leo Wang, Leader
Organizational Affiliation
BTS International
Official's Role
Study Chair
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
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Clinical Study of Wrist Blood Pressure Monitor in Conformance With the ANSI/AAMI SP10 Standard

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