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Panchromoendoscopy Using Oral Indigo Carmine Mixed With Polyethylene Glycol Prep

Primary Purpose

Colonic Polyps

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Chromoendoscopy (Indigo Carmine)
Control
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colonic Polyps focused on measuring polyp

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Patients presenting for screening or surveillance colonoscopy
  • Must be aged 50 to 75 yrs
  • Must be able and willing to sign informed consent

Exclusion criteria:

  • Known Creatinine >1.2
  • Cirrhosis
  • Pregnancy or breast feeding
  • History of anaphylaxis to any dye
  • History of bowel surgery or small bowel obstruction
  • History of aspiration
  • History of dysphagia
  • American Society of Anesthesia class >2
  • History of abnormal liver function test in the last year
  • History of any degree of cytopenia in the last year

Sites / Locations

  • Mayo Clinic in Arizona

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

chromoendoscopy

Control

Arm Description

The intervention arm will have Indigo carmine added to the colonic preperation to perform chromoendoscopy

The control arm will have minimal Indigo carmine added to the colonic prep in a concentration which will not be enough to perform chromoendoscopy

Outcomes

Primary Outcome Measures

Dose of indigo carmine needed to provide adequate chromoendoscopy of the right sided colon
The dose in Indigo Carmine in mg per 1/8 - 1/2 gallon needed to provide adequate staining of the cecum and ascending colon.

Secondary Outcome Measures

Cecal intubation rate
Time to cecal intubation
Withdrawal time
Quality of bowel preparation
The Boston Bowel Preparation Scale will be used to grade the quality of the colonic prep: 0 = Unprepared colon segment with mucosa not seen due to solid stool that cannot be cleared. = Portion of mucosa of the colon segment seen, but other areas of the colon segment not well seen due to staining, residual stool and/or opaque liquid. = Minor amount of residual staining, small fragments of stool and/or opaque liquid, but mucosa of colon segment seen well. = Entire mucosa of colon segment seen well with no residual staining, small fragments of stool or opaque liquid.
Patient tolerance of indigo carmine solution
The rate side effects experienced in the active arm versus the control arm will be compared to determine if side effects experienced are different in both groups. Known common side effect from the Polyethylene based colonic preparation include: Malaise Abdominal distension Anal irritation Nausea Abdominal pain Vomiting Rigors Thirst
Quality of staining of the entire colon
Chromoendoscopy quality: Scoring for 3 areas of the colon will be recorded separately: Right sided, transverse, left sided Distribution of staining in each area: 0 none, covering less than 50% = 1, patchy covering more than 50%=2, staining most of the mucosa (>80%) =3 Intensity of staining: none = 0, poor= 1, fair =visible but not obscuring the vasculature, good= visible and obscuring the vasculature.
Adenoma detection rate
Total number of non rectal serrated polyps detected
Total number of sessile serrated adenoma detected

Full Information

First Posted
June 3, 2013
Last Updated
March 2, 2015
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT01901510
Brief Title
Panchromoendoscopy Using Oral Indigo Carmine Mixed With Polyethylene Glycol Prep
Official Title
Panchromoendoscopy Using Oral Indigo Carmine Mixed With Polyethylene Glycol Prep
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study first is designed to see what dose of indigo carmine ingested orally mixed with the standard colonoscopy prep is needed to provide adequate staining of the right colon. It then will use this adequate staining concentration of Indigo Carmine to study whether this dye will increase the detection of polyps during colonoscopy.
Detailed Description
Colon cancer occurs in 5% of the US population. Currently colon cancer screening is recommended at the age of 50 years old for all patients who are at average risk. Colonoscopy is considered the gold standard test for colon cancer screening. This is partly because colonoscopy not only can detect polyps which are cancer precursors but also can remove them, and thereby detecting cancer and its precursors and preventing cancer. Unfortunately recent data suggest that colonoscopy can miss a significant percentage of polyps, especially on the right side of the colon. It is thought that one of the major reasons for missing polyps in the right side of the colon is the fact that they are flat or sessile serrated adenoma, both of which are more difficult than protruding polyps to identify with ordinary colon preparation and colonoscopes. Chromoendoscopy is the application of dye during colonoscopy to enhance detection of polyps. It has been shown that it improves the detection of polyps and thus has the potential of improving the performance of colonoscopy and increasing the detection of these difficult to detect polyps. It is however cumbersome and time consuming, which has discouraged its use. Indigo carmine, one commonly used dye, is actually FDA approved as a food colorant and can be consumed orally. It is minimally absorbed. In addition it is used intravenously for diagnosis of injuries of the urinary system because it is very rapidly excreted by the kidneys. The investigators believe that taking it orally will be well tolerated, and that any of the dye that is absorbed will be rapidly excreted by the kidneys and thus quickly eliminated without any side effects. Effective staining of the colon with indigo carmine and increased detection of polyps could change the current standard of care for screening for colon cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colonic Polyps
Keywords
polyp

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
chromoendoscopy
Arm Type
Active Comparator
Arm Description
The intervention arm will have Indigo carmine added to the colonic preperation to perform chromoendoscopy
Arm Title
Control
Arm Type
Other
Arm Description
The control arm will have minimal Indigo carmine added to the colonic prep in a concentration which will not be enough to perform chromoendoscopy
Intervention Type
Drug
Intervention Name(s)
Chromoendoscopy (Indigo Carmine)
Other Intervention Name(s)
Indirect chromoendoscopy, Colonoscopy
Intervention Description
Indigo Carmine will be added to the colonic prep to attempt indirect chromoendoscopy
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
The control will have minimal Indigo Carmine added to the colonic prep. This will serve to color the solution blue for blinding but not enough to provide significant staining for chromoendoscopy.
Primary Outcome Measure Information:
Title
Dose of indigo carmine needed to provide adequate chromoendoscopy of the right sided colon
Description
The dose in Indigo Carmine in mg per 1/8 - 1/2 gallon needed to provide adequate staining of the cecum and ascending colon.
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Cecal intubation rate
Time Frame
24 hours
Title
Time to cecal intubation
Time Frame
24 hours
Title
Withdrawal time
Time Frame
24 hours
Title
Quality of bowel preparation
Description
The Boston Bowel Preparation Scale will be used to grade the quality of the colonic prep: 0 = Unprepared colon segment with mucosa not seen due to solid stool that cannot be cleared. = Portion of mucosa of the colon segment seen, but other areas of the colon segment not well seen due to staining, residual stool and/or opaque liquid. = Minor amount of residual staining, small fragments of stool and/or opaque liquid, but mucosa of colon segment seen well. = Entire mucosa of colon segment seen well with no residual staining, small fragments of stool or opaque liquid.
Time Frame
24 hours
Title
Patient tolerance of indigo carmine solution
Description
The rate side effects experienced in the active arm versus the control arm will be compared to determine if side effects experienced are different in both groups. Known common side effect from the Polyethylene based colonic preparation include: Malaise Abdominal distension Anal irritation Nausea Abdominal pain Vomiting Rigors Thirst
Time Frame
30 days
Title
Quality of staining of the entire colon
Description
Chromoendoscopy quality: Scoring for 3 areas of the colon will be recorded separately: Right sided, transverse, left sided Distribution of staining in each area: 0 none, covering less than 50% = 1, patchy covering more than 50%=2, staining most of the mucosa (>80%) =3 Intensity of staining: none = 0, poor= 1, fair =visible but not obscuring the vasculature, good= visible and obscuring the vasculature.
Time Frame
24 hours
Title
Adenoma detection rate
Time Frame
2 weeks
Title
Total number of non rectal serrated polyps detected
Time Frame
2 weeks
Title
Total number of sessile serrated adenoma detected
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Patients presenting for screening or surveillance colonoscopy Must be aged 50 to 75 yrs Must be able and willing to sign informed consent Exclusion criteria: Known Creatinine >1.2 Cirrhosis Pregnancy or breast feeding History of anaphylaxis to any dye History of bowel surgery or small bowel obstruction History of aspiration History of dysphagia American Society of Anesthesia class >2 History of abnormal liver function test in the last year History of any degree of cytopenia in the last year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
M Harrison, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic in Arizona
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States

12. IPD Sharing Statement

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Panchromoendoscopy Using Oral Indigo Carmine Mixed With Polyethylene Glycol Prep

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