Prospective Study of Colon Serrated Polyps
ConditionColon Polyps
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorM.D. Anderson Cancer Center
About this trial
With this study, the investigators plan to review the clinical, epidemiology, pathology, and endoscopic features of colon serrated lesions as well as outcome of endoscopic resection of these lesions. The findings will help us define the natural history of colon serrated lesions, develop techniques for endoscopic management of patients with serrated lesions, and identity areas for improvement. The data will be used for continuing quality improvement and presenting our outcomes at academic meetings and publishing our results in peer reviewed journals.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
Participants undergoing colonoscopy at MD Anderson Cancer Center in Houston, Texas.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Data Collection
Other interventionData collection of endoscopy procedure reports of participants with serrated polyps at MD Anderson Cancer Center in Houston, Texas.
Treatment groups
10,000 Participants
are divided into 1 treatment groupGroup A: Composite Data Collection of Endoscopy of Serrated Polyps1 intervention
Trial outcomes
Primary outcomes
1
Data Review of Colonoscopic Resection of Serrated Colon Polyps
Descriptive tables presented for demographics, polyp counts, colonoscopy experiences, polyp removals and findings. Proportions presented with 95% confidence intervals. Continuous values such as age and times presented with median, minimum and maximum. Comparisons among patient subgroups made with chi-square tests for categorical data and t-tests or the non-parametric alternative, Wilcoxon tests, to compare continuous measures. Graphics such as box plots, trellis plots, bar graphs, or stacked bar graphs used to describe distributions overall and among subgroups.
Time frame
1 daySponsors and contacts
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Source ClinicalTrials.gov