Third Eye Panoramic Device Feasibility Evaluation
Primary Purpose
Colorectal Neoplasms
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Third Eye Panoramic device
Sponsored by
About this trial
This is an interventional diagnostic trial for Colorectal Neoplasms focused on measuring Colonoscopy, Polyps, Adenomas
Eligibility Criteria
Inclusion Criteria:
- The patient is undergoing colonoscopy for screening, for surveillance in follow-up of previous polypectomy or for diagnostic workup.
- The patient must understand and provide written consent for the procedure.
Exclusion Criteria:
- Patients >75 years of age;
- Patients with a history of colonic resection;
- Patients with suspected chronic stricture potentially precluding complete colonoscopy;
- Patients with diverticulitis or toxic megacolon;
- Patients with a history of radiation therapy to abdomen or pelvis;
- Patients who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the patient's participation in this study.
Sites / Locations
- New York Hospital Queens
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
All subjects
Arm Description
All subjects will undergo examination with a Third Eye Panoramic device in conjunction with a standard colonoscope to evaluate the feasibility of using the study device to provide video imaging of areas of the colon that are difficult to evaluate with the colonoscope alone.
Outcomes
Primary Outcome Measures
Device usability factors
Device usability as measured by investigators' qualitative impressions regarding ease of use and any potential interference with function of colonoscope.
Secondary Outcome Measures
Device video factors
Video image quality and ability to view areas behind folds as measured by investigators' qualitative impressions
Patient safety assessed by number of subjects with adverse events as a measure of safety and tolerability
Number of subjects with adverse events
Full Information
NCT ID
NCT02368977
First Posted
February 11, 2015
Last Updated
June 26, 2017
Sponsor
Avantis Medical Systems
1. Study Identification
Unique Protocol Identification Number
NCT02368977
Brief Title
Third Eye Panoramic Device Feasibility Evaluation
Official Title
Third Eye Panoramic Device Feasibility Evaluation
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 12, 2013 (Actual)
Primary Completion Date
October 11, 2017 (Anticipated)
Study Completion Date
October 11, 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Avantis Medical Systems
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will evaluate the feasibility of using the Third Eye Panoramic device in conjunction with standard colonoscopes in a clinical setting.
Patients will undergo a colonoscopy procedure during which the study device will provide video imaging of areas of the colon that are difficult to evaluate with the colonoscope alone.
The utility of the device will be assessed from the impressions of the investigators and from telephone follow-up with subjects to assess for post-procedural complications.
Detailed Description
The purpose of this study is to evaluate the feasibility of using the Third Eye Panoramic device along with a standard colonoscope as a means of enhancing the ability of endoscopists to view areas that are hidden from the view of the colonoscope.
Colonoscopy is generally agreed to be the best method for detecting and removing cancers and pre-cancerous adenomas in the colon. However, numerous studies have demonstrated that from 22% to over 40% of adenomas are missed during standard colonoscopy. More importantly, 12% of large adenomas (at least 1 cm) are missed even by expert endoscopists using meticulous technique with the best available equipment, and these large adenomas are the ones that are most likely to transform into cancer.
Factors such as quality of bowel cleansing and time spent examining the colonic mucosa have been shown to affect miss rates. However, comparison with the results of CT colonography has shown that 2/3 of missed adenomas are located behind folds in the wall of the colon, in areas that are very difficult to see with a standard forward-viewing colonoscope.
When clipped onto the tip of a standard colonoscope, the Third Eye Panoramic device provides two additional miniature video cameras and light sources that offer views to the left side and right side of the colonoscope's tip. These lateral views complement the forward view of the colonoscope's camera to result in a "panoramic" view of over 300°. This extreme wide-angle view allows the endoscopist to examine the areas located behind folds.
In this study, each subject will undergo a colonoscopy procedure utilizing the Third Eye Panoramic device along with a standard colonoscope.
The investigators will evaluate issues related to usability and safety based on their experience and impressions, with telephone follow-up with subjects to assess for any post-procedural complications.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms
Keywords
Colonoscopy, Polyps, Adenomas
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
All subjects
Arm Type
Experimental
Arm Description
All subjects will undergo examination with a Third Eye Panoramic device in conjunction with a standard colonoscope to evaluate the feasibility of using the study device to provide video imaging of areas of the colon that are difficult to evaluate with the colonoscope alone.
Intervention Type
Device
Intervention Name(s)
Third Eye Panoramic device
Intervention Description
A Third Eye Panoramic device will be attached to the tip of the colonoscope and will provide two additional views from laterally-oriented video cameras during the colonoscopy procedure.
Primary Outcome Measure Information:
Title
Device usability factors
Description
Device usability as measured by investigators' qualitative impressions regarding ease of use and any potential interference with function of colonoscope.
Time Frame
1 hour (average duration of procedure)
Secondary Outcome Measure Information:
Title
Device video factors
Description
Video image quality and ability to view areas behind folds as measured by investigators' qualitative impressions
Time Frame
1 hour (average duration of procedure)
Title
Patient safety assessed by number of subjects with adverse events as a measure of safety and tolerability
Description
Number of subjects with adverse events
Time Frame
At time of procedure and up to 48 hours after completion of procedure
10. Eligibility
Sex
All
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
The patient is undergoing colonoscopy for screening, for surveillance in follow-up of previous polypectomy or for diagnostic workup.
The patient must understand and provide written consent for the procedure.
Exclusion Criteria:
Patients >75 years of age;
Patients with a history of colonic resection;
Patients with suspected chronic stricture potentially precluding complete colonoscopy;
Patients with diverticulitis or toxic megacolon;
Patients with a history of radiation therapy to abdomen or pelvis;
Patients who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the patient's participation in this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Moshe Rubin, MD
Organizational Affiliation
New York Hospital Queens - Weill Cornell Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York Hospital Queens
City
Flushing
State/Province
New York
ZIP/Postal Code
11355
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26457029
Citation
Rubin M, Lurie L, Bose K, Kim SH. Expanding the view of a standard colonoscope with the Third Eye Panoramic cap. World J Gastroenterol. 2015 Oct 7;21(37):10683-7. doi: 10.3748/wjg.v21.i37.10683.
Results Reference
derived
Learn more about this trial
Third Eye Panoramic Device Feasibility Evaluation
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