Comparison of on Demand Sedation With Study Method Versus on Demand Sedation With Conventional Method for Performing Colonoscopy for Colorectal Cancer Screening and Surveillance

Sponsor
East Bay Institute for Research and Education (Other)
Overall Status
Unknown status
CT.gov ID
NCT00920751
Collaborator
(none)
100
1
2

Study Details

Study Description

Brief Summary

Hypothesis

  1. Study method achieves lower requirement for medications

  2. Study method increases overall cecal intubation with comparable assessment of current experience and patient willingness to repeat future colonoscopy compared with conventional colonoscopy

  3. Study method results in reduction in medication-related (cardiorespiratory) complications, faster turn around of patients, compared with conventional colonoscopy

  4. Study method improves bowel preparation and increases polyp pickup rate

Colorectal cancer (CRC) screening for the high and the low risk healthy asymptomatic VA patients is being promoted (VHA directive). Compliance with this Directive will result in an increased number of VA patients undergoing colonoscopy. The demand for colonoscopy far exceeds the capacity available to perform the procedure in the VA system. The conventional practice for colonoscopy at VA facilities across the country is to perform colonoscopy under conscious sedation with air insufflation. Efficiency is governed by the fact that sedated patients require time and space for recovery and these are major limiting factors in the current setting for the use of colonoscopy for CRC screening.

Methods that maintain a high success rate and good patient assessment improve overall compliance for surveillance colonoscopy. Our preliminary experience showed that patients are able to complete successful colonoscopy without sedation in 52% of cases when colonoscopy was aided by a water infusion in lieu of air insufflation method. In this group of patients, the shortened recovery time means a quick turn around of patient and a more efficient endoscopy service. Patients are able to communicate better with the staff and physician regarding their problem and discharge instructions, and not subjected to the amnesic effect of sedation. Next day follow-up of patient by telephone contact which requires commitment of staff time can be obviated.

If this randomized study confirms the success of our preliminary findings and this technique is adopted by more endoscopists, a larger number of VA patients may benefit from less sedation complications and at the same time allow for more efficient colonoscopy screening services.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Water infusion
  • Procedure: Air insufflation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Participant)
Primary Purpose:
Screening
Official Title:
Comparison of on Demand Sedation With Study Method Versus on Demand Sedation With Conventional Method for Performing Colonoscopy for Colorectal Cancer Screening and Surveillance
Study Start Date :
Mar 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: Water infusion

Water infusion in lieu of air insufflation during colonoscope insertion

Procedure: Water infusion
Water infusion in lieu of air insufflation during colonoscope insertion

Active Comparator: Air insufflation

Conventional air insufflation colonoscopy

Procedure: Air insufflation
Conventional air insufflation colonoscopy

Outcome Measures

Primary Outcome Measures

  1. Primary outcome - success of cecal intubation without sedation [1 year]

Secondary Outcome Measures

  1. Diagnostic yield, patients' current experience, willingness to repeat future colonoscopy, turn around time, and staff rating of satisfaction, and medication-related complications. [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adult (> 50 years old), male and female patients

  • Scheduled and consented for screening or surveillance colonoscopy

  • Accept randomization to the study or the conventional method

  • Agree to complete study questionnaires will be considered for enrollment

  • Normal healthy patients or patients with mild systemic disease, ASA 1 or ASA 2

Exclusion Criteria:
  • Patients who decline to participate, are unable to give informed consent or to complete the questionnaires due to language or other difficulties will be excluded. Excluded patients will be managed by usual procedures at the Sacramento VAMC

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sacramento VA Medical Center Mather California United States 95655

Sponsors and Collaborators

  • East Bay Institute for Research and Education

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00920751
Other Study ID Numbers:
  • EBIRE-GI-003
First Posted:
Jun 15, 2009
Last Update Posted:
Jun 15, 2009
Last Verified:
Jun 1, 2009
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 15, 2009