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Panoramic Screening by Complete Colonoscopy in the Management of Colorectal Adenomas

Panoramic Screening by Complete Colonoscopy in the Management of Colorectal Adenomas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03961893
Acronym
G-EYE-ADR
Enrollment
164
Registered
2019-05-23
Start date
2020-01-21
Completion date
2023-06-19
Last updated
2023-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Adenoma

Keywords

colonoscopy, g-eye, adenomas

Brief summary

Colonoscopy is the gold standard for colorectal cancer prevention by allowing the resection of superficial colorectal adenomas or adenocarcinomas. This protection, more effective in the left colon than in the right colon, is imperfect and there are some adenomas and cancers omitted during colonoscopy. The G-EYE colonoscope equipped with an integrated distal balloon would better unfold the haustrations and stabilize the endoscope. Thus, the detection rate of adenomas would be improved by this better vision. The main objective of this study is to confirm that the use of the G-EYE colonoscope allows better detection of adenomatous polyps, decrease the rate of omitted adenomes and then is more effective.

Interventions

DEVICEG-EYE first and standard colonoscope

Patients undergo two successive colonoscopies, first balloon-assisted colonoscopy (G-EYE device) and then standard colonoscopy

DEVICEstandard colonoscope first and G-EYE

Patients undergo two successive colonoscopies, first standard colonoscopy and then balloon-assisted colonoscopy (G-EYE device)

Sponsors

Institut Paoli-Calmettes
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Prospective, single-phase, two-stage, randomized phase II study

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Indication of complete colonoscopy for classic indications (bleeding, abdominal pain, transit disorders) or for family and personal antecedents of adenomas or colorectal cancers with the need for endoscopic control, 2. FIT + test (current blood test for stool used for mass screening in France), PET-CT fixation, 3. Consent of participation signed, 4. Affiliation to a social security scheme, or beneficiary of such a scheme.

Exclusion criteria

1. Non-optimal preparation (boston score \<7 or segment \<2), 2. Adenomatous polyposis, familial or assimilated (juvenile, etc.), 3. Pregnant or likely to be pregnant (without effective contraception) or breastfeeding, 4. Patient in emergency or deprived of liberty or placed under the authority of a tutor, 5. Patient considered geographically socially or psychologically unable to comply with the study procedure and the medical follow-up.

Design outcomes

Primary

MeasureTime frameDescription
Rate of missed adenomas during standard colonoscopy and balloon-assisted colonoscopy (G-EYE device)Colonoscopy timeRate between the number of adenomas detected by the second examination and the number of adenomas detected by the two inspections

Secondary

MeasureTime frameDescription
Adenoma detected rate during standard colonoscopy and balloon-assisted colonoscopy (G-EYE device) in male and femaleColonoscopy timeRate between the number of detected adenomas with each endoscope and the number of colonoscopies performed in male and female
Rate of complicationsColonoscopy time and 1 month afterGlobal and for each arm
Rate of missed advanced adenomas during standard colonoscopy and balloon-assisted colonoscopy (G-EYE device)Colonoscopy timeRate between the number of advanced adenomas detected by the second examination and the number of advanced adenomas detected by the two inspections
Adenoma detected rate during standard colonoscopy and balloon-assisted colonoscopy (G-EYE device) in FIT+ subgroupColonoscopy timeRate between the number of detected adenomas with each endoscope and the number of colonoscopies performed in FIT+ subgroup
G-EYE assistance for endoscope stabilizationColonoscopy timeYes or no
Rate of missed adenomas during standard colonoscopy and balloon-assisted colonoscopy (G-EYE device) in positive fetal immunochemical test (FIT+) subgroupColonoscopy timeRate between the number of adenomas detected by the second examination and the number of adenomas detected by the two inspections in FIT+ subgroup

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026