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Endoscopy Device

Endocuff Vision Assisted Colonoscopy for Sessile Serrated Adenoma

N/A
Waitlist Available
Research Sponsored by University of California, Davis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up time point of assessment will be when pathology results are made available 2 weeks after procedure. data will be collected through study completion, analyzed and reported up to 6 months after study completion.
Awards & highlights

Study Summary

This trial will compare standard colonoscopy to colonoscopy with a new attachment, Endocuff Vision, to see if the attachment increases detection of a certain kind of precancerous growth.

Eligible Conditions
  • Sessile Serrated Adenoma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time point of assessment will be when pathology results are made available 2 weeks after procedure. data will be collected through study completion, analyzed and reported up to 6 months after study completion.
This trial's timeline: 3 weeks for screening, Varies for treatment, and time point of assessment will be when pathology results are made available 2 weeks after procedure. data will be collected through study completion, analyzed and reported up to 6 months after study completion. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Sessile Serrated Adenoma Detection Rate
Secondary outcome measures
Adenoma Detection Rate
Colonoscope Withdrawal Time
Differences in Quality of Bowel Preparation
+5 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Endocuff Vision Assisted ColonoscopyExperimental Treatment1 Intervention
Patients randomly assigned to this group will receive colonoscopy with the use of the Endocuff Vision distal attachment.
Group II: Standard ColonoscopyActive Control1 Intervention
Patients randomly assigned to this group will receive standard colonoscopy without the use of a distal attachment.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Endocuff Vision Assisted Colonoscopy
2019
N/A
~430

Find a Location

Who is running the clinical trial?

University of California, DavisLead Sponsor
911 Previous Clinical Trials
4,709,156 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals of advanced age authorized to partake in this experiment?

"Applicants to this study must be between 45 and 85 years of age."

Answered by AI

How many individuals are engaged in this clinical research?

"Right, clinicaltrials.gov verifies that this trial is currently accepting participants and has been since May 1st 2019. The most recent edits were made on September 16th 2021; the aim is to recruit 1374 patients from a single location."

Answered by AI
Recent research and studies
~72 spots leftby Apr 2025