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A Comparative Clinical Trial of the TensorTip, a Novel Non Invasive Device for Measurement Blood Parameters

Primary Purpose

Anemia, Diabetes, Heart Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Non invasive peripheral blood monitoring
Sponsored by
Cnoga Medical Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Anemia

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or female, age > 18
  2. Patients with cardiovascular disease and/or with diabetes mellitus type I or II and/or with COPD.
  3. Patients receiving coronary artery bypass with or without valve repair.
  4. Able to sign an informed consent.

Exclusion Criteria:

  1. Refusal to sign an informed consent and to participate in the study.
  2. Participant plans to enroll in another other clinical trial of an investigational agent while participating in this study.
  3. Below the age of 18.

Sites / Locations

  • Atlantic Health - Morristown Memorial Hospital- Cardiovascular Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Non Invasive Monitoring

Arm Description

Intervention: Device: Non invasive peripheral blood monitoring

Outcomes

Primary Outcome Measures

Comparison of the TensorTip Accuracy Against Hospital Periodical Readings.
To validate the parameters with similar measures obtained with standard invasive techniques in hospitalized patients. Methodology: Eligible real time color signal obtained by the TensorTip shall be recorded simultaneously during the monitoring performed. An algorithm shall be designed according to the blood color distribution to each parameter and a final test shall be recorded signals. Statistical analysis for each parameter shall perform on the entire eligible recorded signals. Determination of Accuracy: Err = √(1/N ∑N (Ref(k)-NewDevice(k)) ^2 ) (k=1) For each parameter a satisfactory result is considered when Err satisfies the industry requirement. Results viewing Each parameter comparative study shall be presented on a (X,Y) plan versus a regression line where X - represents the results measured by TensorTip and Y - the reference results.

Secondary Outcome Measures

Full Information

First Posted
August 29, 2010
Last Updated
January 30, 2019
Sponsor
Cnoga Medical Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT01196533
Brief Title
A Comparative Clinical Trial of the TensorTip, a Novel Non Invasive Device for Measurement Blood Parameters
Official Title
A Comparative Clinical Trial to Assess the Accuracy of the TensorTip, a Novel Non Invasive Device for the Measurement of Physiological and Blood Chemistry Parameters
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cnoga Medical Ltd.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Aim: The aim of the clinical trial is to study the accuracy of the TensorTip device compared with registered (FDA-approved) invasive and non-invasive devices. Hypothesis: Human physiological biomarkers may be measured from the color distribution of the internal or external (skin) tissue. The technology of the TensorTip finger-mounted device is based on the color distribution of the peripheral blood tissue, which enables the measurement of certain biomarkers and vital signs under consideration.
Detailed Description
The TensorTip (previously named Soft Touch) is a novel non invasive Finger tip device that. The Tensor Tip is a non-invasive device which was designed and aimed to measure a wide range of physiological and bio-parameters such as blood glucose, hemoglobin and hematocrit, blood PH, oxygen saturation SpO2, blood carbon dioxide, blood pressure, peripheral pulse and more based on the temporarily color distribution of the tissue under consideration. The Tensor Tip is based on real time color image sensor, real time photographing the fingertip tissue. A color image sensor of the type used in the Tensor Tip enables a wide range of information in the spectral, resolution, dynamic range and time domains enabling further investigation of the blood chromatic changes as a function body physiology. The concept behind this investigation reflects the idea that a change in human physiology condition would temporarily change the blood pigmentation. The present study is aimed to assess the accuracy of the novel device in measuring all the above mentioned parameters by recording AS IS the change of the fingertip color tissue while simultaneous recording the standard invasive measured parameters on daily or periodic routine in the hospitalized patients. This vast data recordings (tissue and references) enable the Tensor tip to analyze a particular bio parameter. The tensor tip is calibrated to a certain bio parameter based on the vast data set collected. The bio parameter under consideration are: Arterial Systolic and Diastolic, MAP, PA systolic, PA Diastolic, CO, Heart rate, Stroke volume, WBC, RBC, Hgb, HCT ,Iron, PLT, PH, PCO2, PO2, HCO3, SaO2 , Na, K, Cl, CO2, Bun, Cr, Gluc, HGB (A1C),TBiLi, LDL, HDL. This study hopes to demonstrate the connection between blood color pigmentation and certain bio parameters for simplifying monitoring procedure and particular home monitoring.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Diabetes, Heart Disease, High Blood Pressure, Hypotension, Metabolic Diseases, Respiratory Diseases

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
94 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Non Invasive Monitoring
Arm Type
Experimental
Arm Description
Intervention: Device: Non invasive peripheral blood monitoring
Intervention Type
Device
Intervention Name(s)
Non invasive peripheral blood monitoring
Intervention Description
non invasive monitoring
Primary Outcome Measure Information:
Title
Comparison of the TensorTip Accuracy Against Hospital Periodical Readings.
Description
To validate the parameters with similar measures obtained with standard invasive techniques in hospitalized patients. Methodology: Eligible real time color signal obtained by the TensorTip shall be recorded simultaneously during the monitoring performed. An algorithm shall be designed according to the blood color distribution to each parameter and a final test shall be recorded signals. Statistical analysis for each parameter shall perform on the entire eligible recorded signals. Determination of Accuracy: Err = √(1/N ∑N (Ref(k)-NewDevice(k)) ^2 ) (k=1) For each parameter a satisfactory result is considered when Err satisfies the industry requirement. Results viewing Each parameter comparative study shall be presented on a (X,Y) plan versus a regression line where X - represents the results measured by TensorTip and Y - the reference results.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female, age > 18 Patients with cardiovascular disease and/or with diabetes mellitus type I or II and/or with COPD. Patients receiving coronary artery bypass with or without valve repair. Able to sign an informed consent. Exclusion Criteria: Refusal to sign an informed consent and to participate in the study. Participant plans to enroll in another other clinical trial of an investigational agent while participating in this study. Below the age of 18.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank Smart, M.D
Organizational Affiliation
Chairman of the Cardiovascular Medicine Department at Morritwon Memorial Hospital and Atlantic Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yosef Segman, PhD
Organizational Affiliation
Cnoga Medical Ltd.
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Donna Hesari, BSN
Organizational Affiliation
Atlantic Health System, Department of Cardiovascular Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Atlantic Health - Morristown Memorial Hospital- Cardiovascular Medicine
City
Morristown
State/Province
New Jersey
ZIP/Postal Code
07962-1905
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Links:
URL
http://www.cnoga.com
Description
Sponsor website.

Learn more about this trial

A Comparative Clinical Trial of the TensorTip, a Novel Non Invasive Device for Measurement Blood Parameters

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