Water Exchange Colonoscopy Clinical Trial
Official title:
Prospective RCT of Water Exchange (WE) vs. WE Plus Cap-Assisted Colonoscopy
Verified date | November 2023 |
Source | VA Office of Research and Development |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a study to compare two different, but normally, used methods of colonoscopy in patients undergoing colonoscopy without sedation. There will be two arms in this study: WE (water exchange) control, and WE (water exchange) plus cap (placed at tip of the colonoscope). The patient will prepare himself/herself for the colonoscopy as per normal instructions and he/she will be given the information for the study at that time so that he/she can make a decision to participate in the study. The control method will use water instead of air during insertion of the colonoscope. The study method will use a cap that will fit onto the end of the colonoscope plus water during insertion of the colonoscope. This study will assess if the study method is less painful than the control method.
Status | Completed |
Enrollment | 280 |
Est. completion date | October 28, 2022 |
Est. primary completion date | October 28, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 50 Years to 80 Years |
Eligibility | Inclusion Criteria: - Informed/educated (about pros and cons of the unsedated option) Veterans undergoing: - diagnostic - surveillance (follow up of polyps) - screening (first-time) colonoscopy at participating sites - choosing scheduled unsedated colonoscopy for any reason (lack of escort, personal preference) Exclusion Criteria: - decline to be randomized - unable to give consent or respond to questionnaires - history of colon surgery - active inflammatory bowel disease - lower gastrointestinal bleeding (except for occult blood or FIT positive in the context of colon cancer screening) - therapeutic colonoscopy (e.g., hemostasis, removal of large polyp) - proctosigmoidoscopy - bidirectional endoscopy - inadequate consumption of bowel preparation - known history of severe diverticulosis or diverticulitis - history of abdominal surgery previously requiring sedation for colonoscopy - current narcotic/anxiolytic medication use - prior unsuccessful experience with unsedated colonoscopy - emergent colonoscopy - evidence of colonic obstruction based on pre-colonoscopy clinical evaluation - current participation in other studies - medical condition that could increase the risk associated with colonoscopy - active cardiac - or pulmonary disease - or other serious disease - medical condition that would preclude a benefit from colonoscopic screening - cancer - or any terminal illness - prosthetic heart valve - anticoagulant therapy - nonmedical problems - psychiatric disorders - excessive use of alcohol - need for special precautions in performing colonoscopy - antibiotic prophylaxis - request of on demand sedation |
Country | Name | City | State |
---|---|---|---|
United States | VA Palo Alto Health Care System, Palo Alto, CA | Palo Alto | California |
United States | VA Northern California Health Care System, Mather, CA | Sacramento | California |
United States | VA Greater Los Angeles Healthcare System, Sepulveda, CA | Sepulveda | California |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development | VA Northern California Health Care System, VA Palo Alto Health Care System |
United States,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Real Time Maximum Insertion Pain | Pain during insertion reported to the unblinded assisting nurse, visual analogue scale, VAS: 0=none, 10=most severe. The highest pain score will be tabulated for analysis. Timing of data collection will be at the discretion of the nurse to minimize bias by colonoscopist behavior. | Insertion pain was measured during the duration of the colonoscopy procedure, which lasted on average for about 1 hour | |
Secondary | Proportion of Patients With No Insertion Pain | Proportion of patients who report no pain during insertion of the colonoscope. | Pain was measured during the duration of the colonoscopy procedure, which lasted on average for about 1 hour | |
Secondary | Insertion Time | Time to cecum (clock display on monitor), faster insertion is a quality marker | Insertion time in minutes was measured during the duration of the colonoscopy procedure, which lasted on average for about 1 hour | |
Secondary | Right Colon Adenoma Detection Rate (ADR) | Right colon Adenoma Detection Rate (ADR) is the proportion of patients with at least one adenoma in the part of the colon between the cecum and the hepatic flexure. | Adenoma Detection Rate (ADR) was measured during the duration of the colonoscopy procedure, which lasted on average for about 1 hour |
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