Comparisons of SWI, WWI and CI in Potentially Difficult Colonoscopy.

December 29, 2018 updated by: Shenzhen People's Hospital

Comparisons of Sigmoid-colon Water Immersion, the Whole Colon Water Immersion and Carbon Dioxide (CO2) Insufflation on Cecal Intubation Time in Potentially Difficult Colonoscopy by Difficult Colonoscopy Score(DCS) >1.

Colonoscopy insertion is technically challenging, time-consuming, and painful, especially for the sigmoid. It is reported that the difficult colonoscopy score (DCS) >1 can predict the difficulty during colonoscopy. Patients with DCS>1 had longer insertion time, higher pain score and needed more abdominal compression and position changes. As reported, water-aided method colonoscopy examination is an important and useful method because it reduces discomfort and increases cecal intubation rate compared with usual air insufflation method. But a longer time was consumed for scope insertion and cecal intubation in the traditional water-aided method colonscopy(the whole water immersion). To avoid these disadvantages ,we modified whole colon water immersion(WWI) method to the sigmoid colon water immersion(SWI), where the most difficult and painful part of colonoscopy resides. If water immersion is limited to the sigmoid colon in such patients, would it be more efficient and less time consuming?

The aim of this study was to investigate the application of water-aided method on cecal intubation time in potentially difficult colonoscopy. This prospective, randomized controlled study allocated patients who's difficult colonoscopy score(DCS) >1 (18-80 years) to sigmoid-colon water immersion(SWI), whole colon water immersion(WWI) or carbon dioxide (CO2) insufflation (CI) group (1:1:1). The primary outcome was cecal intubation time. The secondary outcomes included the maximum pain score (0=none,10=most severe) during the insertion phase in left, transverse and right colon; cecal intubation rate; adenoma detection rate(ADR); bowel preparation quality; withdrawal time(from cecum to rectum excluding time for biopsy and polypectomy); willingness to undergo a repeat unsedated colonoscopy; number of abdominal compressions, position change during the insertion. Patients were educated to understand the meaning of visual analogue scale (VAS) (0 = no pain, 10 = most severe) and to report their maximum pain scores during the insertion through each colonic segment. Descriptive statistics were used to summarize demographic and baseline data. Analyses were performed with SPSS software version 24.0 for Windows (SPSS Inc, IBM Company).

Study Overview

Status

Completed

Conditions

Detailed Description

Introduction: Colonoscopy insertion is technically challenging, time-consuming, and painful, especially for the sigmoid. Many factors have been found to affect the difficulty of colonoscope insertion, such as age, gender, body mass index, history of abdominal surgery and operator ect. It is reported that the difficult colonoscopy score (DCS) >1 can predict the difficulty during colonoscopy. DCS=1*A(1 if age≥65y, 0 if <65y) + 2*B (1 if BMI <18.5, 0 if BMI≥18.5) + 1*C (1 if colonoscopist is junior, 0 if senior)+ 1*S(1 if sleep quality was fair or bad, 0 if excellent or good). Patients with DCS>1 had longer insertion time, higher pain score and needed more abdominal compression and position changes. For these potentially difficult cases we can use special intubation techniques such as water-aided or cap-assisted method at the very start to avoid of excessive insertion time, increased discomfort and even unnecessary adverse events.

Water-aided method colonoscopy examination is an important and useful method because it reduces discomfort and increases cecal intubation rate compared with usual air insufflation method. This examination is usually performed using two different methods: water immersion and water exchange. In the water immersion method, the water is infused into the colon beginning with the scope inserted into the anus during examination until the scope reaches the cecum. The water is evacuated during colonoscope withdrawal. In the water exchange method, the water is evacuated during colonoscope advancement until the cecum is reached. The air pump of the endoscopy machine is turned off during examination in both procedures. The aim of this study was to investigate the application of water-aided method on cecal intubation time in potentially difficult colonoscopy. We chose water immersion method rather than water exchange for this evaluation because water immersion, characterized by suction removal of the infused water predominantly during withdrawal, is more appropriate for reducing the cecal intubation time. Further more ,as reported, left-colon water exchange(LWE) shorten the insertion time while preserving the benefits of whole colon water exchange(WWE). We modified whole colon water immersion(WWI) method to the sigmoid colon water immersion(SWI), where the most difficult and painful part of colonoscopy resides. If water immersion is limited to the sigmoid colon in such patients, would it be more efficient and less time consuming? Methods:This prospective, randomized controlled study allocated patients who's difficult colonoscopy score(DCS) >1 (18-80 years) to sigmoid-colon water immersion(SWI), whole colon water immersion(WWI) or carbon dioxide (CO2) insufflation (CI) group (1:1:1). Patients were randomized to SWI, WWI or CI group according to a computer-generated randomization list in 1:1:1 ratio. Group assignments were revealed immediately before the insertion of colonoscopy by a researcher , who did not participate in data collection and data analysis. The monitor screen was placed over the head of patients to keep them from knowing the insertion method. Endoscopists and assisting nurses were not blinded. For the bowel preparation, all patients were instructed to take low-fiber diet for lunch and clear liquid diets for dinner the day before examination. They ingested 2L of PEG powder (WanHe Pharmaceutical Co, Shenzhen, China) diluted with water within 2 h, between 4:00 AM and 5:00 AM on the day of the examination. Those with chronic constipation received an additional 2L of PEG solution on the evening prior to the examination. Drinking more clear water and pacing back and forth after purgatives were encouraged to enhance laxative effect. The time interval between preparation and colonoscopy was limited to less than 5 h to ensure the quality of bowel preparation.

Endoscopic procedure Two endoscopists (WBH and YJ) with extensive experience in both air (>5000) and water methods (>500) performed the colonoscopies. The standard adult colonoscope (EC-600WM, Fujinon, Beijing) was used. Patients were placed in the left lateral position at the beginning of the procedure. Maneuvers such as abdominal compression and position change were implemented if needed (e.g. when looping, paradoxical movement or lack of advancement occurred). Successful cecal intubation was confirmed by the visualization of appendiceal orifice or ileocecal valve with the tip of the colonoscope touching the base of the cecum. For the AI method, air was insufflated through out the whole procedure for advancement and inspection when needed. In the WWI method,the air supply was turn off until the cecum was reached. For adequate lumen distention to advance the colonoscope tip, warm water which stored in 1L bottles and maintained 37°C with a water bath, was instilled intermittently into the colon through the auxiliary working channel of colonoscope using a footswitch-controlled flushing pump. For patients allocated to SWI group, air pump would be turned off and the procedure would be switched from water immersion method to air insufflation method after successful passage through the descending sigmoid junction.

The primary outcome was cecal intubation time. The secondary outcomes included the maximum pain score (0=none,10=most severe) during the insertion phase in left, transverse and right colon; cecal intubation rate; adenoma detection rate (ADR); bowel preparation quality; withdrawal time(from cecum to rectum excluding time for biopsy and polypectomy); willingness to undergo a repeat unsedated colonoscopy; number of abdominal compressions, position change during the insert.

Descriptive statistics were used to summarize demographic and baseline data. Quantitative variables are expressed as means and standard deviations and analyzed by ANOVA followed by Bonferroni test for multiple comparisons. Categorical variables in three groups were compared with chi-square test or Fisher exact test when appropriate. All p-Values were two-sided and those < 0.05 were considered to be significant. Analyses were performed with SPSS software version 24.0 for Windows (SPSS Inc, IBM Company).

Study Type

Interventional

Enrollment (Actual)

240

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

    • Guangdong
      • Shenzhen, Guangdong, China, 518000
        • Shenzhen People's Hospital

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

18 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. patients undergoing diagnostic, screening or surveillance colonoscopy
  2. their difficult colonoscopy score(DCS) >1. DCS=1*A(1 if age≥65y, 0 if <65y) + 2*B (1 if BMI <18.5, 0 if BMI≥18.5) + 1*C(1 if colonoscopist is junior, 0 if senior)+ 1*S(1 if sleep quality was fair or bad, 0 if excellent or good).

Exclusion Criteria:

  1. history of colorectal resection;
  2. sedated colonoscopy;
  3. severe colonic stricture or obstructing tumor known before colonoscopy;
  4. current pregnancy;
  5. hemodynamic instability
  6. inability to provide informed consent.

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
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: whole colon water immersion group
whole colon water immersion group: the air supply was turn off until the cecum was reached. For adequate lumen distention to advance the colonoscope tip, warm water which stored in 1L bottles and maintained 37°C with a water bath, was instilled intermittently into the colon through the auxiliary working channel of colonoscope using a footswitch-controlled flushing pump
we chose water immersion method instead of the triaditional method of carbon dioxide (CO2) insufflation.
Other Names:
  • carbon dioxide (CO2) insufflation
EXPERIMENTAL: sigmoid water immersion group
sigmoid water immersion group: air pump would be turned off and the procedure would be switched from water immersion method to air insufflation method after successful passage through the descending sigmoid junction.
we chose water immersion method instead of the triaditional method of carbon dioxide (CO2) insufflation.
Other Names:
  • carbon dioxide (CO2) insufflation
PLACEBO_COMPARATOR: carbon dioxide (CO2) insufflation
carbon dioxide (CO2) insufflation group: carbon dioxide (CO2) was insufflated through out the whole procedure for advancement and inspection when needed.
we chose water immersion method instead of the triaditional method of carbon dioxide (CO2) insufflation.
Other Names:
  • carbon dioxide (CO2) insufflation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
cecal intubation time
Time Frame: 3 months
the time the colonoscope advanced from the anus to the cecum
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
maximum pain score
Time Frame: 3 months
0=none, 10=most severe
3 months
withdrawal time
Time Frame: 3 months
from cecum to rectum excluding time for biopy and polypectomy
3 months

Collaborators and Investigators

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

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.

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 (ACTUAL)

April 3, 2018

Primary Completion (ACTUAL)

November 26, 2018

Study Completion (ACTUAL)

December 26, 2018

Study Registration Dates

First Submitted

May 28, 2018

First Submitted That Met QC Criteria

June 17, 2018

First Posted (ACTUAL)

June 27, 2018

Study Record Updates

Last Update Posted (ACTUAL)

January 2, 2019

Last Update Submitted That Met QC Criteria

December 29, 2018

Last Verified

April 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • SWI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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