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Breath Analysis Technique to Diagnose Pulmonary Embolism

Primary Purpose

Pulmonary Embolism

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
BreathScreen PE
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Pulmonary Embolism focused on measuring Capnography, Thromboembolism, Arthroplasty, D-dimer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Phase I Inclusion Criteria: Experienced or is scheduled for at least one of the following: Hip or knee replacement surgery Hip or acetabular fracture surgery Pelvic fracture Decompression for spinal stenosis surgery Scoliosis corrective surgery Craniotomy surgery for brain tumor Surgery for any of the following cancers: bladder, colon (including caecum and rectum), kidney, ovary, pancreas, or uterus Phase I Exclusion Criteria: Currently undergoing treatment for PE or has received treatment for PE in the 4 weeks prior to study entry Hospitalized for fewer than 2 days Anatomic abnormality that would prevent use of a mouthpiece Living situation that makes follow-up difficult (e.g., homeless, incarcerated) Phase II Inclusion Criteria: Clinical suspicion of PE with signs or symptom suggestive of PE within 24 hours of presentation and at least one risk factor for PE, as defined under the criteria as outlined in this protocol CTA of pulmonary arteries ordered by clinical care providers 18 years or older or an emancipated 17 year old Written informed consent Phase II Exclusion Criteria: Hemodynamic instability, including patients with a systolic blood pressure less than 90 mm Hg Severe respiratory distress or the inability to breathe room air without the sensation of severe dyspnea Pulse oximetry reading that declines more than 10% when exogenous oxygen is discontinued with accompanying worsening or new dyspnea Intubated Cannot breathe through the mouth owing to anatomic, physical or mental limitation No fixed address, no telephone number, are from out of town or have other reason to suspect difficulty with follow-up Incarceration Known active tuberculosis Prior PE or DVT with history of medical noncompliance with oral anticoagulation therapy based upon a history of unplanned subtherapeutic INR measurements (less than 1.5) Active PE within previous 6 months and currently under treatment with anticoagulation Pregnant Disallowed medications: treatment with any fibrinolytic agent within 48 hours prior to enrollment

Sites / Locations

  • Carolinas Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

BreathScreen PE + D-dimer

Arm Description

CO2/O2 ratio will be measured using the Breath Screen PE device. D-dimer levels will also be collected.

Outcomes

Primary Outcome Measures

Phase I: Percentage Change in the Postoperative End Tidal CO2/O2 Ratio and D-dimer Concentration Relative to the Preoperative Measurement
Median postoperative change in end tidal CO2/O2 ratio calculated as 100% * [(postoperative-preoperative)/(preoperative)]
Phase II: Probability of Pulmonary Embolism Diagnosis by D-dimer Alone vs. D-Dimer Plus CO2/O2 for Pulmonary Embolism Diagnosed by CT Scan.
D-dimer > 499 ng/ml, etCO2/O2 < 0.28, Pulmonary Embolism diagnosed by CT scan

Secondary Outcome Measures

Full Information

First Posted
August 24, 2006
Last Updated
April 19, 2022
Sponsor
Wake Forest University Health Sciences
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), WFD Ventures Incorporated
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1. Study Identification

Unique Protocol Identification Number
NCT00368836
Brief Title
Breath Analysis Technique to Diagnose Pulmonary Embolism
Official Title
Expired CO2/O2 Analysis to Diagnose Pulmonary Embolism
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), WFD Ventures Incorporated

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A pulmonary embolism (PE) is a blockage in one of the arteries of the lungs, and is usually caused by a traveling blood clot. The D-dimer blood test is currently used to diagnose PEs, but it is not always accurate for individuals who have recently undergone surgery or who have inflammatory-provoking diseases. The purpose of this study is to evaluate the effectiveness of the Carboximeter, a new PE diagnostic device that measures carbon dioxide (CO2) and oxygen (O2) output, in individuals at risk for developing PEs.
Detailed Description
PE is the second leading cause of sudden, unexpected death in the United States. In 90% of the cases, it is caused by deep vein thrombosis: a blood clot forms in a vein, travels through the bloodstream, and lodges in the lungs. PE symptoms vary, and can include cough, shortness of breath, chest pain, rapid breathing, or increased heart rate. Some medical procedures and diseases activate inflammation and blood coagulation, thereby making individuals more vulnerable to PE. Surgery, kidney dialysis, cancer, connective tissue diseases, infectious diseases, and being over 70 years old put individuals at increased risk for developing PEs. A common screening test for PE is the D-dimer blood test, which measures the level of a specific protein that is released following a PE. This test, however, has proven to be an unreliable diagnostic tool for individuals who are at high risk for PE. A more reliable diagnostic tool is needed. The Carboximeter is a new device that measures the ratio of CO2/O2 pressure in an individual's expired breath. By monitoring these components, researchers may be able to accurately diagnose PEs in high risk individuals. The purpose of this study is to evaluate the effectiveness of the Carboximeter at diagnosing PE in individuals at risk for developing PEs. This study will be conducted in two phases. In Phase I, CO2/O2 ratio and D-dimer levels will be measured prior to and following orthopedic or cancer-related surgery in 100 individuals at risk for developing PEs. In Phase II, the same measurements will be carried out on 350 high risk individuals who are experiencing PE symptoms. These individuals will also undergo computed tomography (CT) angiography and venography, in which blood flow will be visualized using x-rays. A follow-up evaluation will occur 30 days later. If any participant from Phase I or II experiences a PE or a medical condition that affects their lungs, such as asthma or chronic obstructive pulmonary disease (COPD), researchers may schedule a follow-up evaluation to obtain repeat measurements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Embolism
Keywords
Capnography, Thromboembolism, Arthroplasty, D-dimer

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
475 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BreathScreen PE + D-dimer
Arm Type
Experimental
Arm Description
CO2/O2 ratio will be measured using the Breath Screen PE device. D-dimer levels will also be collected.
Intervention Type
Device
Intervention Name(s)
BreathScreen PE
Intervention Description
One minute of breath collection by tidal breathing into the BreathScreen PE and blood draw for D-dimer level
Primary Outcome Measure Information:
Title
Phase I: Percentage Change in the Postoperative End Tidal CO2/O2 Ratio and D-dimer Concentration Relative to the Preoperative Measurement
Description
Median postoperative change in end tidal CO2/O2 ratio calculated as 100% * [(postoperative-preoperative)/(preoperative)]
Time Frame
Pre-op measurement: the morning of surgery. Post-op measurement: the latter of postoperative day 3 or hospital discharge
Title
Phase II: Probability of Pulmonary Embolism Diagnosis by D-dimer Alone vs. D-Dimer Plus CO2/O2 for Pulmonary Embolism Diagnosed by CT Scan.
Description
D-dimer > 499 ng/ml, etCO2/O2 < 0.28, Pulmonary Embolism diagnosed by CT scan
Time Frame
Measured at 45 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Phase I Inclusion Criteria: Experienced or is scheduled for at least one of the following: Hip or knee replacement surgery Hip or acetabular fracture surgery Pelvic fracture Decompression for spinal stenosis surgery Scoliosis corrective surgery Craniotomy surgery for brain tumor Surgery for any of the following cancers: bladder, colon (including caecum and rectum), kidney, ovary, pancreas, or uterus Phase I Exclusion Criteria: Currently undergoing treatment for PE or has received treatment for PE in the 4 weeks prior to study entry Hospitalized for fewer than 2 days Anatomic abnormality that would prevent use of a mouthpiece Living situation that makes follow-up difficult (e.g., homeless, incarcerated) Phase II Inclusion Criteria: Clinical suspicion of PE with signs or symptom suggestive of PE within 24 hours of presentation and at least one risk factor for PE, as defined under the criteria as outlined in this protocol CTA of pulmonary arteries ordered by clinical care providers 18 years or older or an emancipated 17 year old Written informed consent Phase II Exclusion Criteria: Hemodynamic instability, including patients with a systolic blood pressure less than 90 mm Hg Severe respiratory distress or the inability to breathe room air without the sensation of severe dyspnea Pulse oximetry reading that declines more than 10% when exogenous oxygen is discontinued with accompanying worsening or new dyspnea Intubated Cannot breathe through the mouth owing to anatomic, physical or mental limitation No fixed address, no telephone number, are from out of town or have other reason to suspect difficulty with follow-up Incarceration Known active tuberculosis Prior PE or DVT with history of medical noncompliance with oral anticoagulation therapy based upon a history of unplanned subtherapeutic INR measurements (less than 1.5) Active PE within previous 6 months and currently under treatment with anticoagulation Pregnant Disallowed medications: treatment with any fibrinolytic agent within 48 hours prior to enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jefferey A. Kline, MD
Organizational Affiliation
Indiana University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Carolinas Medical Center
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28203
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16836693
Citation
Kline JA, Hogg M. Measurement of expired carbon dioxide, oxygen and volume in conjunction with pretest probability estimation as a method to diagnose and exclude pulmonary venous thromboembolism. Clin Physiol Funct Imaging. 2006 Jul;26(4):212-9. doi: 10.1111/j.1475-097X.2006.00672.x.
Results Reference
background
PubMed Identifier
24232703
Citation
Kline JA, Watts J, Courtney D, Lee YY, Hwang S. Severe pulmonary embolism decreases plasma L-arginine. Eur Respir J. 2014 Mar;43(3):906-9. doi: 10.1183/09031936.00171913. Epub 2013 Nov 14. No abstract available.
Results Reference
derived
PubMed Identifier
22284935
Citation
Kline JA, Hogg MM, Courtney DM, Miller CD, Jones AE, Smithline HA. D-dimer threshold increase with pretest probability unlikely for pulmonary embolism to decrease unnecessary computerized tomographic pulmonary angiography. J Thromb Haemost. 2012 Apr;10(4):572-81. doi: 10.1111/j.1538-7836.2012.04647.x.
Results Reference
derived
PubMed Identifier
20448094
Citation
Kline JA, Hogg MM, Courtney DM, Miller CD, Jones AE, Smithline HA, Klekowski N, Lanier R. D-dimer and exhaled CO2/O2 to detect segmental pulmonary embolism in moderate-risk patients. Am J Respir Crit Care Med. 2010 Sep 1;182(5):669-75. doi: 10.1164/rccm.201001-0129OC. Epub 2010 May 6.
Results Reference
derived

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Breath Analysis Technique to Diagnose Pulmonary Embolism

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