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Procedure
Cap-Assisted Colonoscopy for Reduced Pain and Insertion Time (VA Trial)
N/A
Waitlist Available
Led By Felix W Leung, MD
Research Sponsored by VA Greater Los Angeles Healthcare System
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 2 hours
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new method for colonoscopy that uses water and a small cap to make the procedure less painful and more effective for veterans. The water method for colonoscopy, which involves water infusion instead of air, has been shown to reduce patient discomfort and sedation requirements in several studies.
Who is the study for?
This trial is for male and female Veterans who opt for unsedated colonoscopy, whether it's for screening, diagnosis, or surveillance. Participants must be able to consent and complete questionnaires. Those with a history of certain abdominal surgeries, current heavy medication use, or conditions that complicate colonoscopy are excluded.
What is being tested?
The study compares two methods during a colonoscopy: the Water Exchange (WE) method alone versus WE plus Cap-assisted Colonoscopy (WECAC). The goal is to see if adding a cap reduces pain more than WE alone and if it improves the procedure time and detection rate of adenomas in the proximal colon.
What are the potential side effects?
While not explicitly listed in your information provided, typical side effects from these procedures may include discomfort or mild pain due to gas insufflation, bloating, cramping sensations during insertion of the scope or when using water exchange techniques.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Real-time maximum insertion pain(RTMIP) score
Secondary study objectives
Insertion time
Proportion with no insertion pain
Proximal colon ADR
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: WE plus cap(WECAC)Experimental Treatment2 Interventions
The procedure of this group is similar with WE group, except a cap will be fitted onto the end of the colonoscope.
Group II: Water exchange (WE)Active Control1 Intervention
This group will have the air in the colon removed and replaced with water to guide the insertion of the colonoscope.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
cap
2017
N/A
~710
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The Water Exchange (WE) method reduces Real-time Maximum Insertion Pain (RMIP) by infusing water instead of air during colonoscope insertion, minimizing bowel distension and discomfort. Cap-Assisted Colonoscopy (CAC) adds a cap to the colonoscope, aiding in smoother navigation and reducing mucosal trauma.
These techniques are important for RMIP patients as they enhance comfort during the procedure and improve adenoma detection rates, which is vital for effective colorectal cancer screening.
Find a Location
Who is running the clinical trial?
VA Greater Los Angeles Healthcare SystemLead Sponsor
51 Previous Clinical Trials
8,161 Total Patients Enrolled
VA Palo Alto Health Care SystemFED
93 Previous Clinical Trials
57,928 Total Patients Enrolled
VA Northern California Health Care SystemFED
18 Previous Clinical Trials
3,191 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have an artificial heart valve.You have a medical condition that could make colonoscopy risky for you.You have a medical condition that won't allow you to benefit from colonoscopy screening.You have a history of ongoing inflammation in your intestines.You have had bleeding in your intestines or rectum in the past.You have had a colonoscopy as part of a medical treatment.You will not be able to undergo a procedure called bidirectional endoscopy.You have a history of severe diverticulosis or diverticulitis.You are currently taking prescription medicine for pain or anxiety.You have previously had a colonoscopy without sedation, and it was not successful.You are currently taking medication to prevent blood clots.You do not have any non-medical issues that could interfere with your participation in the study.
Research Study Groups:
This trial has the following groups:- Group 1: WE plus cap(WECAC)
- Group 2: Water exchange (WE)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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