A Dual Tandem Study - SC vs. CAD-EYE vs. CAD-EYE With G-EYE

Sponsor
Dr. Horst Schmidt Klinik GmbH (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05318495
Collaborator
(none)
372
1
4
9
41.2

Study Details

Study Description

Brief Summary

Single-center, four-arm dual-tandem, randomized, open-label study involving the following devices:

  1. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

  2. CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

  3. The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Condition or Disease Intervention/Treatment Phase
  • Device: Standard Colonoscopy
  • Device: CAD-EYE
  • Device: G-EYE
N/A

Detailed Description

Single-center, four-arm dual-tandem, randomized, open-label study involving the following devices:

  1. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

  2. CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

  3. The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Total of up to 372 patients will be randomized,186 to each of the two tandems

Study Design

Study Type:
Interventional
Anticipated Enrollment :
372 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
A Dual Tandem Study Comparing the Adenoma Detection and Miss-rate of SC to That of Artificial Intelligence (CAD-EYE) Aided Colonoscopy and to That of Artificial Intelligence (CAD-EYE) and G-EYE® Aided Colonoscopy.
Actual Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Standard Colonoscopy+CAD-EYE followed by Standard Colonoscopy

CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: Standard Colonoscopy
The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: CAD-EYE
CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

Active Comparator: Standard Colonoscopy followed by Standard Colonoscopy+CAD-EYE

CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: Standard Colonoscopy
The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: CAD-EYE
CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

Experimental: Standard Colonoscopy+CAD-EYE+G-EYE followed by Standard Colonoscopy

CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI). The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Device: Standard Colonoscopy
The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: CAD-EYE
CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

Device: G-EYE
The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Active Comparator: Standard Colonoscopy followed by Standard Colonoscopy+CAD-EYE+G-EYE

CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas. The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI). The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Device: Standard Colonoscopy
The Standard Colonoscope is a high-definition colonoscope employing advanced optical filtering and enhancement techniques - blue light imaging (BLI) and linked color imaging (LCI).

Device: CAD-EYE
CAD-EYE is an artificial intelligence software, used in real-time during the colonoscopy procedure for aiding the identification and characterization of polyps and adenomas.

Device: G-EYE
The G-EYE® balloon is a reusable (reprocessable) balloon permanently installed on the distal tip of a standard colonoscope, and is also intended to assist in flattening colonic folds and control the colonoscope's field of view and tip positioning.

Outcome Measures

Primary Outcome Measures

  1. Additional adenoma detection yield [6 weeks]

    additional adenoma detection yield (represented by the miss rate) of CAD-EYE and G-EYE® colonoscopy over standard coloscopy compared to the additional adenoma detection yield of CAD-EYE aided colonoscopy over standard colonoscopy

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Screening and surveillance population for Adenoma and CRC.

  2. The patient must understand and sign a written informed consent for the procedure.

Exclusion Criteria:
  1. Subjects with inflammatory bowel disease;

  2. Subjects with a personal history of hereditary polyposis syndrome;

  3. Subjects with suspected chronic stricture potentially precluding complete colonoscopy;

  4. Subjects with diverticulitis or toxic megacolon;

  5. Subjects with prior colonic surgery (exclusion appendectomy)

  6. Subjects with a history of radiation therapy to abdomen or pelvis;

  7. Pregnant or lactating female subjects;

  8. Subjects who are currently enrolled in another clinical investigation.

  9. Subjects with current oral or parenteral use of anticoagulants, not considered eligible by the investigator.

  10. Subjects with recent (within the last 3 mounts) coronary ischemia or CVA (stroke)

  11. Any patient condition deemed too risky for the study by the investigator

Contacts and Locations

Locations

Site City State Country Postal Code
1 Helios Dr. Horst Schmidt Kliniken Wiesbaden Germany 65199

Sponsors and Collaborators

  • Dr. Horst Schmidt Klinik GmbH

Investigators

  • Principal Investigator: Ralf Kiesslich, Prof., Helios Dr. Horst Schmidt Kliniken Wiesbaden

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prof. Dr. Ralf Kiesslich, Prof., Dr. Horst Schmidt Klinik GmbH
ClinicalTrials.gov Identifier:
NCT05318495
Other Study ID Numbers:
  • Dual Tandem
First Posted:
Apr 8, 2022
Last Update Posted:
Apr 8, 2022
Last Verified:
Apr 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 8, 2022