search
Back to results

Breath Analysis as an Additional Test for Colorectal Cancer Screening to Reduce the Number of Unnecessary Colonoscopies (SCREENER)

Primary Purpose

Colorectal Cancer, Polyp of Colon, Colorectal Neoplasms

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
AeonoseTM
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colorectal Cancer focused on measuring Volatile organic compounds, VOC, Colorectal cancer, Advanced adenoma, Breath test, Electronic nose, eNose, Aeonose

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients between the ages of 55 and 75 years referred for a colonoscopy procedure after a positive FIT test, according to the population based CRC screening program in the Netherlands

Exclusion Criteria:

  • Prior surgical resection of any portion of the colon
  • History of any type of malignancy, not including squamous cell carcinoma (SCC) and basal cell carcinoma (BCC)
  • Current active colitis or history of polyposis syndrome

Sites / Locations

  • Radboud university medical center

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients referred for colonoscopy

Arm Description

Outcomes

Primary Outcome Measures

Diagnostic accuracy in distinguishing colorectal carcinoma from healthy controls
The diagnostic accuracy, in terms of sensitivity and specificity, of the AeonoseTM in distinguishing between patients with and without CRC.

Secondary Outcome Measures

Diagnostic accuracy in distinguishing advanced adenoma from healthy controls
Sensitivity and specificity
Reproducibility
The variation in VOC analysis results between two separate time points. The binary results from the eNose analysis will be presented in a scatterplot and a receiver operating characteristics curve (ROC-curve). Cohen's kappa statistic will be applied to determine interobserver agreement between the eNose results of 2 different timepoints (>2 weeks apart)
Acceptance rate
The acceptance rate of using the AeonoseTM in participating patients.

Full Information

First Posted
April 20, 2020
Last Updated
January 3, 2023
Sponsor
Radboud University Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT04357158
Brief Title
Breath Analysis as an Additional Test for Colorectal Cancer Screening to Reduce the Number of Unnecessary Colonoscopies
Acronym
SCREENER
Official Title
Breath analysiS as an Additional Test for ColoREctal cancEr screeNing to rEduce the Number of unnecessaRy Colonoscopies
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
May 25, 2020 (Actual)
Primary Completion Date
January 5, 2022 (Actual)
Study Completion Date
July 5, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In the past decade, the demand for colonoscopy procedures has increased significantly since the introduction of population-based colorectal cancer (CRC) screening in many western countries. Post-polypectomy surveillance will increase the number of colonoscopy procedures conducted each year even further. The invasive nature of colonoscopy and the associated health-care costs warrant the development of a new non-invasive test to reduce the number of unnecessary colonoscopies. These days, many countries use a non-invasive fecal test for CRC screening which is easy to perform at home, but test characteristics such as sensitivity and specificity are suboptimal. Multiple studies have already shown that volatile organic compound (VOC) analysis has a high diagnostic accuracy for CRC and Advanced Adenomas. An additional VOC analysis, for example through breath testing, in patients with a positive fecal immunochemical test (FIT) may reduce the number of unnecessary colonoscopies. The aim of this study is to validate the diagnostic accuracy of the AeonoseTM to distinguish patients with CRC from healthy controls, and to assess reproducibility of test results.
Detailed Description
Rationale: An electronic nose (eNose) is an artificial olfactory system that analyses volate organic compounds (VOCs) in exhaled breath. Exhaled human breath is mainly composed of inorganic compounds, inert gases and VOCs. VOCs are exhaled in very low concentrations and reflect pathological processes such as inflammation, oxidation, infection and neoplasms. The perspective is that metabolic and biochemical processes in several pathological situations cause different endogenous VOCs to arise, were they can serve as non-invasive biomarkers for certain diseases. Primary objective: To evaluate if the use of an additional breath test (AeonoseTM) for patients with a positive FIT-test can reduce the number of unnecessary colonoscopies. Secondary objectives: External validation of results for CRC and (advanced) adenoma detection established in a previous studies (second study not yet published). (15) To evaluate if VOC profiles in breath are similar at two different time points. Acceptance rate of using the AeonoseTM device for VOC analysis in participating patients. Study population: Patients between the ages of 55 and 75 years old with a positive FIT-test referred for a colonoscopy procedure. Estimated sample size: 750 participants Intervention: Participants will be asked to breath through the AeonoseTM for 5 minutes during pre-colonoscopy intake and just prior to the procedure to assess reproducibility (with >2 weeks in between). There are no risks, nor benefits for the participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Polyp of Colon, Colorectal Neoplasms
Keywords
Volatile organic compounds, VOC, Colorectal cancer, Advanced adenoma, Breath test, Electronic nose, eNose, Aeonose

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This is a multicenter prospective cohort study in participants eligible for colonoscopy with suspicion for (pre)malignant lesions of the colon
Masking
None (Open Label)
Allocation
N/A
Enrollment
750 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients referred for colonoscopy
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
AeonoseTM
Intervention Description
All participants will be asked to breathe into an electronic nose (eNose, the AeonoseTM, The eNose Company, Zutphen, the Netherlands) for 5 minutes during the pre-colonoscopy intake and just prior to the procedure to assess reproducibility (with >2 weeks in between).
Primary Outcome Measure Information:
Title
Diagnostic accuracy in distinguishing colorectal carcinoma from healthy controls
Description
The diagnostic accuracy, in terms of sensitivity and specificity, of the AeonoseTM in distinguishing between patients with and without CRC.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Diagnostic accuracy in distinguishing advanced adenoma from healthy controls
Description
Sensitivity and specificity
Time Frame
12 months
Title
Reproducibility
Description
The variation in VOC analysis results between two separate time points. The binary results from the eNose analysis will be presented in a scatterplot and a receiver operating characteristics curve (ROC-curve). Cohen's kappa statistic will be applied to determine interobserver agreement between the eNose results of 2 different timepoints (>2 weeks apart)
Time Frame
12 months
Title
Acceptance rate
Description
The acceptance rate of using the AeonoseTM in participating patients.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients between the ages of 55 and 75 years referred for a colonoscopy procedure after a positive FIT test, according to the population based CRC screening program in the Netherlands Exclusion Criteria: Prior surgical resection of any portion of the colon History of any type of malignancy, not including squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) Current active colitis or history of polyposis syndrome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter D Siersema, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud university medical center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands

12. IPD Sharing Statement

Learn more about this trial

Breath Analysis as an Additional Test for Colorectal Cancer Screening to Reduce the Number of Unnecessary Colonoscopies

We'll reach out to this number within 24 hrs