Prospective Randomized Controlled Trial Comparing Water and Air Colonoscopy in a Community Based Setting

May 26, 2017 updated by: University of California, Davis

Prospective Randomized Controlled Trial Comparing Water Exchange Colonoscopy and Air Colonoscopy in a Community Based Setting

The purpose of this study is to determine if screening colonoscopy performed on adults with the water exchange method, as opposed to the air method, will have a higher adenoma detection rate.

Study Overview

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

Interventional

Enrollment (Actual)

178

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Elk Grove, California, United States, 95758
        • Elk Grove PCN, University of California, Davis

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.

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.
Air will be infused into the colon during colonoscopy.

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.
Presence of adenoma detected anywhere between the cecum and the splenic flexure
Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is collected only once per patient.

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.
Adenoma detection anywhere in the colon during colonoscopy.
Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient.
Sedation requirements
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
The amount of sedation required to complete the patient's colonoscopy.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Total procedure time
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
The total time it takes to complete colonoscopy.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Cecal intubation time
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
The time it takes to reach the cecum during colonoscopy.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
The need for patient's position to be changed from left lateral to other positions, to enable advancement of the colonoscope forward.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
The need to stiffen the colonoscope to enable to forward movement of the scope during procedure
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
Need for abdominal pressure by endoscopist's assistant during procedure to enable forward movement of colonoscope.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
Assessment of length of the colonoscope inserted into the colon to reach the cecum.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
Procedure-related pain score
Time Frame: Data collected during and post procedure after recovery from sedation, which is usually within 1 hour post procedure
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.
Data collected during and post procedure after recovery from sedation, which is usually within 1 hour post procedure
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.
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.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
Assessment of volume of water introduced into the colon during procedure.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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.
Assessment of patient's perception about the 2 methods of colonoscopy.
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length.
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
Data collected when pathology is available, typically 3-10 days after the patient's procedure. Data is only collected once per patient
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
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
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
This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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
This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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
This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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
This will be collected at the time of their procedure appointment which is expected to be 2 to 3 hours in length
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
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
Smoking history
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
Alcohol consumption
Time Frame: This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length
This will be collected at their procedure appointment which is expected to be 2 to 3 hours in length

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sooraj Tejaswi, M.D., University of California, Davis

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2014

Primary Completion (Actual)

April 1, 2015

Study Completion (Actual)

April 1, 2015

Study Registration Dates

First Submitted

November 2, 2012

First Submitted That Met QC Criteria

November 14, 2012

First Posted (Estimate)

November 20, 2012

Study Record Updates

Last Update Posted (Actual)

May 31, 2017

Last Update Submitted That Met QC Criteria

May 26, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 297959
  • 297959-4 (Other Identifier: UC Davis)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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