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Ambient Lighting During Colonoscopy and Its Effect on Adenoma Detection Rate and Eye Fatigue

Use of Ambient Lighting During Colonoscopy and Its Effect on Adenoma Detection Rate and Eye Fatigue: a Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04441242
Enrollment
1109
Registered
2020-06-22
Start date
2017-01-01
Completion date
2018-06-30
Last updated
2024-10-04

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

Conditions

Colon Adenomatous Polyp, Colorectal Cancer Screening

Brief summary

A retrospective and prospective study to determine if the use of ambient lighting during screening colonoscopy is well tolerated and if ambient lighting will help physicians maintain adenoma detection rates while decreasing symptoms of eye strain as the day progresses.

Detailed description

This study is a a single-center study at an independent community-based teaching hospital comparing adenoma detection rate in screening colonoscopies performed in low lighting with those performed with ambient lighting (75-150 lux). All cases included in the study involved adult patients undergoing screening colonoscopy with a participating gastroenterologist. Diagnostic colonoscopies, history of colon resection, colorectal cancer, and cases performed in children, pregnant women, and prisoners were excluded from analysis. Cases involving gastroenterology fellows were also excluded. Retrospective data was collected over a six month period from January 2017 to June 2017, followed by a prospective arm the during the same calendar months the subsequent year (January 2018 to June 2018).

Interventions

OTHERAmbient lighting

Use of ambient lighting (75-150 lux) in endoscopy room.

OTHERLow lighting

Use of low lighting (\<75 lux) in endoscopy room.

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Adults undergoing screening colonoscopy * Procedure performed by a participating gastroenterologist

Exclusion criteria

* Any diagnostic colonoscopies * History of colon resection * History of colorectal cancer * Children * Pregnant women * Prisoners * Cases involving trainees, including gastroenterology fellows

Design outcomes

Primary

MeasureTime frameDescription
Change in adenoma detection rate6 monthsAdenoma detection rate, comparing change from first case of the day to the last. Ranges from 0-99%, with greater increases adenoma detection rate (ADR) being more favorable.
Eye strain score6 monthsEye strain score, as calculated from survey responses completed by physicians. Ranges from 0 - 60, with lower scores indicating less severe symptoms (therefore, lower scores are more favorable).

Secondary

MeasureTime frameDescription
Adenoma detection rate (overall)Participants each assessed on one day during 6 month study periodOverall adenoma detection rate. Ranges from 0% to 100%. Higher ADR is more favorable.
Adenoma detection rate (first case vs last case of the day)Participants each assessed on one day during 6 month study periodAdenoma detection rate, comparing first case of the day to the last. Ranges from from -99 to 99%, with greater numbers (increases) being more favorable.
Satisfaction by staff6 monthsSatisfaction by staff involved in endoscopy, based on survey responses

Countries

United States

Outcome results

None listed

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