- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01729416
Prospective Randomized Controlled Trial Comparing Water and Air Colonoscopy in a Community Based Setting
Prospective Randomized Controlled Trial Comparing Water Exchange Colonoscopy and Air Colonoscopy in a Community Based Setting
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Screening colonoscopy with removal of pre-cancerous adenomas was recently shown to result in a 53% reduction in mortality from colon cancer. While this clearly validates the practice of screening colonoscopy, missed adenomas, especially in the proximal colon, defined as including cecum, ascending colon, and transverse colon, remains a concern. This was demonstrated in a study of 183 patients who underwent back-to-back colonoscopies. In this population the overall miss rate for adenomas was 24% with proximal adenomas missed more often (27%) than left colon adenomas (21%). Another study looked at 4192 patients in the SEER (Surveillance, Epidemiology, and End Results) Medicare database who developed "interval cancers", that is colon cancer in a patient who had a colonoscopy done in the previous 6-36 months. These interval cancers were predominantly in the proximal colon (Proximal 68%, Distal 19.5%, rectum 10.4%, and unspecified 2.1%). This also suggests that pre-cancerous lesions are being missed in the proximal colon. As such a method that can increase proximal adenoma detection rate would be a welcome change.
One such emerging technique which shows promise for improving adenoma detection rate is water colonoscopy. In one of the early studies employing the water method a trend towards a higher ADR in the water method group was recognized (37% vs. 26%). The observation prompted a retrospective analysis of 1178 cases of screening and surveillance colonoscopy performed by a single endoscopist at the Sacramento VAMC, which showed an overall ADR (presence of at least one adenoma) of 27% with air colonoscopy whereas that for the water method colonoscopy was 35% (p=0.007). In a subsequent combined analysis of two prospective RCT of air vs. water colonoscopy for screening and surveillance using scheduled unsedated colonoscopy [5] and on-demand sedation [6], more patients were found to have at least one diminutive adenoma in the proximal colon in the water method group than in the air group (28% vs. 14%, respectively, p=0.0298). Another quasi randomized study of screening patients performed at Phoenix VAMC using high definition equipment confirmed a significantly higher overall ADR with the water method (n=177) compared with the air method (n=191) (57% vs. 46%) (p=0.03). The odds of detecting an adenoma was 81% higher with the water method (OR 1.81; 95% CI: 1.12-2.90) and independent of age, body mass index (BMI), current smoking and alcohol use, withdrawal time & quality of bowel preparation. In the proximal colon ADR was significantly higher in patients examined with the water method than with air method (46% vs. 35%) (p=0.03), particularly for adenomas <10 mm in size (38% vs. 25%) (p=007). These encouraging preliminary data reflect the potential benefits of water method colonoscopy.
Our current research question is whether this benefit is seen in a community based population as opposed to the VA population which is mostly male and Caucasian.
The investigators plan to perform a prospective, randomized controlled trial comparing proximal adenoma detection rate between a water exchange colonoscopy group and an air colonoscopy group. The investigators intend to employ scheduled sedation, instead of on-demand sedation, to continue the current protocol in place at our institution.
Patients in both the study arms will undergo a split bowel preparation before colonoscopy.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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Elk Grove, California, United States, 95758
- Elk Grove PCN, University of California, Davis
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age ≥50 years
- Individuals able to provide informed consent
- Individuals presenting for average-risk colorectal cancer screening by colonoscopy
- Individuals presenting for surveillance of adenomatous/sessile serrated colon polyps as per the US multi-society taskforce on colorectal cancer
Exclusion Criteria:
- Patients who decline to participate
- Prior partial or complete colectomy
- Patients with history of inflammatory bowel disease (ulcerative colitis or Crohn's disease)
- Patients with prior history of colorectal cancer
- Patients with history of screening colonoscopy within the past 10 years
- Patients with history of familial polyposis syndromes (Familial Adenomatous Polyposis, Lynch Syndrome)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Water Exchange Colonoscopy
The intervention will be water exchange colonoscopy in patients who are randomized to have screening colonoscopy with water exchange colonoscopy.
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We will turn off the air pump. The colonoscope will be inserted into the rectum and gently advanced. We will suction air pockets as scope is advanced towards the cecum. Water will be infused when encountering closed up lumen. All the infused water will be suctioned out. We will use all other techniques used with conventional air method as needed. For example abdominal pressure, shortening of scope to reduce looping, change of patient position etc. We will turn on air pump once cecum reached, or if unsuccessful with water method to open up a close lumen or to go past a tight turn. On withdrawal we will continue air insufflation as needed, and closely examine for polyps and remove all visualized polyps. If there is any residual fluid, it will be suctioned out as the scope is withdrawn. |
Active Comparator: Air colonoscopy
The intervention will be colonoscopy using the traditional air method in patients who are randomized to have screening colonoscopy with air colonoscopy.
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Air will be infused into the colon during colonoscopy.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proximal Adenoma detection
Time Frame: Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is collected only once per patient.
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Presence of adenoma detected anywhere between the cecum and the splenic flexure
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Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is collected only once per patient.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total adenoma detection
Time Frame: Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient.
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Adenoma detection anywhere in the colon during colonoscopy.
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Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient.
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Sedation requirements
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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The amount of sedation required to complete the patient's colonoscopy.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Total procedure time
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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The total time it takes to complete colonoscopy.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Cecal intubation time
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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The time it takes to reach the cecum during colonoscopy.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Patient position change during procedure
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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The need for patient's position to be changed from left lateral to other positions, to enable advancement of the colonoscope forward.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Use of colonoscope stiffener during procedure
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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The need to stiffen the colonoscope to enable to forward movement of the scope during procedure
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Abdominal pressure by assistant during procedure
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Need for abdominal pressure by endoscopist's assistant during procedure to enable forward movement of colonoscope.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Length of colonoscope at time of cecal intubation
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Assessment of length of the colonoscope inserted into the colon to reach the cecum.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Procedure-related pain score
Time Frame: Data collected during and post procedure after recovery from sedation, which is usually within 1 hour post procedure
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Assessment of discomfort due to the procedure, as possible during procedure, and post procedure after recovery from sedation, being cognizant of limitations posed by sedation and attendant amnesia.
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Data collected during and post procedure after recovery from sedation, which is usually within 1 hour post procedure
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Reason for air insufflation, and length of colon when air insufflation started, while performing water colonoscopy
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Assessment of percentage of patient requiring air insufflation when water colon fails to open colonic lumen, and site of colon where this is most likely to happen.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Volume of water used during water colonoscopy
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Assessment of volume of water introduced into the colon during procedure.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Patient perception regarding air and water colonoscopy
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Assessment of patient's perception about the 2 methods of colonoscopy.
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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Advanced adenoma detection rate
Time Frame: Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient
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Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient
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Type of polypectomy (cold biopsy/cold snare/snare cautery/need for submucosal injection/need for clip placement)
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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Bowel preparation quality by Boston Bowel Prep Scale
Time Frame: This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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Post procedure recovery time
Time Frame: This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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Serrated polyp detection rate
Time Frame: This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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Procedure time- morning versus afternoon
Time Frame: This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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Body Mass Index (BMI)
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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Smoking history
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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Alcohol consumption
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sooraj Tejaswi, M.D., University of California, Davis
Publications and helpful links
General Publications
- Leung FW, Harker JO, Jackson G, Okamoto KE, Behbahani OM, Jamgotchian NJ, Aharonian HS, Guth PH, Mann SK, Leung JW. A proof-of-principle, prospective, randomized, controlled trial demonstrating improved outcomes in scheduled unsedated colonoscopy by the water method. Gastrointest Endosc. 2010 Oct;72(4):693-700. doi: 10.1016/j.gie.2010.05.020. Epub 2010 Jul 8.
- Lai EJ, Calderwood AH, Doros G, Fix OK, Jacobson BC. The Boston bowel preparation scale: a valid and reliable instrument for colonoscopy-oriented research. Gastrointest Endosc. 2009 Mar;69(3 Pt 2):620-5. doi: 10.1016/j.gie.2008.05.057. Epub 2009 Jan 10.
- Leung J, Mann S, Siao-Salera R, Ransibrahmanakul K, Lim B, Canete W, Samson L, Gutierrez R, Leung FW. A randomized, controlled trial to confirm the beneficial effects of the water method on U.S. veterans undergoing colonoscopy with the option of on-demand sedation. Gastrointest Endosc. 2011 Jan;73(1):103-10. doi: 10.1016/j.gie.2010.09.020.
- Zauber AG, Winawer SJ, O'Brien MJ, Lansdorp-Vogelaar I, van Ballegooijen M, Hankey BF, Shi W, Bond JH, Schapiro M, Panish JF, Stewart ET, Waye JD. Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med. 2012 Feb 23;366(8):687-96. doi: 10.1056/NEJMoa1100370.
- Rex DK, Cutler CS, Lemmel GT, Rahmani EY, Clark DW, Helper DJ, Lehman GA, Mark DG. Colonoscopic miss rates of adenomas determined by back-to-back colonoscopies. Gastroenterology. 1997 Jan;112(1):24-8. doi: 10.1016/s0016-5085(97)70214-2.
- Leung FW, Aharonian HS, Leung JW, Guth PH, Jackson G. Impact of a novel water method on scheduled unsedated colonoscopy in U.S. veterans. Gastrointest Endosc. 2009 Mar;69(3 Pt 1):546-50. doi: 10.1016/j.gie.2008.08.014.
- Leung JW, Do LD, Siao-Salera RM, Ngo C, Parikh DA, Mann SK, Leung FW. Retrospective analysis showing the water method increased adenoma detection rate - a hypothesis generating observation. J Interv Gastroenterol. 2011 Jan;1(1):3-7. doi: 10.4161/jig.1.1.14585.
- Leung FW, Leung JW, Siao-Salera RM, Mann SK. The water method significantly enhances proximal diminutive adenoma detection rate in unsedated patients. J Interv Gastroenterol. 2011 Jan;1(1):8-13. doi: 10.4161/jig.1.1.14587.
- Ramirez FC, Leung FW. A head-to-head comparison of the water vs. air method in patients undergoing screening colonoscopy. J Interv Gastroenterol. 2011 Jul;1(3):130-135. doi: 10.4161/jig.1.3.18512. Epub 2011 Jul 1.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
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