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Colorectal Polyps Screening With Low-dose CT Colonoscopy

Primary Purpose

Polyps, Colorectal Neoplasm

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
CT colonoscopy(normal dose)
CT colonoscopy (low dose)
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Polyps

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects with gastrointestinal symptoms potentially suggestive of colorectal cancer, such as diarrhea, constipation, abdominal pain or discomfort, rectal bleeding, iron-deficiency anemia, and unintended weight loss.
  • Subjects with pathological confirmed colorectal cancer or polyps that need follow-up examination.
  • Subjects with written consents

Exclusion Criteria:

  • Subjects with acute colitis
  • Acute diverticulitis
  • Inguinal hernia including colon
  • Colorectal surgery or endoscopic biopsy or resection of polyps within 6 months
  • Known or suspected as colon perforated
  • Complete intestinal obstruction
  • Pregnant or lactating women

Sites / Locations

  • Xi jing HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

CT colonoscopy(normal dose)

CT colonoscopy(low dose)

Arm Description

Perform CT colonoscopy with full bowel preparation and inflated colon, CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kilovolts peak (kVp), 100-200mA

Perform CT colonoscopy with full bowel preparation and inflated colon, CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kVp, 20-100mA

Outcomes

Primary Outcome Measures

Sensitivity and specificity of low-dose CTC for the polyp detection
return the number of polyps detected by low-dose CTC for each participant, sensitivity and specificity of low-dose CTC for the polyp detection can be derive from it with OC results as reference.

Secondary Outcome Measures

CT radiation
Record the dose-length product of each CT scan for CTC participants and radiation dose of each scan can be derived from it.
Sensitivity and specificity of CTC for the detection of polyps with different shapes
Return the shape and location information of polyps detected by OC and CTC for each participant to reflect the CTC performance for the detection of polyps with different morphologies, especially for three major morphologic categories: sessile, pedunculated, and flat.
Sensitivity and specificity of CTC for the detection of poly malignancy
Return the histological types of polyps biopsied through OC after pathologic examination to reflect the CTC performance for the detection of polyp malignancy, especially the capability to differentiate adenomatous polyps from hyperplastic polyps.

Full Information

First Posted
January 24, 2017
Last Updated
July 18, 2018
Sponsor
Xijing Hospital
Collaborators
Air Force Military Medical University, China
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1. Study Identification

Unique Protocol Identification Number
NCT03064828
Brief Title
Colorectal Polyps Screening With Low-dose CT Colonoscopy
Official Title
Colorectal Adenoma Screening by Low-dose CT Colonoscopy With Computer-aided Detection
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xijing Hospital
Collaborators
Air Force Military Medical University, China

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This preliminary clinical trial aims to evaluate the performance of the low-dose CT colonoscopy (CTC) with computer aided detection (CAD) on polyps detection compared with optical colonoscopy (OC), and explore the possible clinical routine for integrated use of CT colonoscopy and optical colonoscopy OC in colorectal cancer screening.
Detailed Description
CT colonoscopy (CTC), also referred to as virtual colonoscopy (VC), utilizes computer virtual-reality techniques to navigate inside a three-dimensional patient-specific colon model reconstructed from abdominal CT images, looking for colonic lesions, full bowel preparation and colon inflation are needed to perform CTC examination. The clinical trial consists of two major parts: Comparative study on the performance of CTC and OC: 50 subjects will be recruited in this part with written consents. With full bowel preparation, all the volunteers receive CT scans first with inflated colon, then OC followed by the same day, and necessary pathological analysis thereafter. The performance of CTC based on high-resolution CT data, including the number of polyps detected, size, position, etc, will be validated by that of OC with the paired comparison. Integrate use of low-dose CTC with OC for colorectal cancer screening: After the validation of CTC performance, in this part, another 50 subjects will be recruited to explore the integrated use of CTC with OC as a possible and efficient workflow for colorectal cancer screening. In this part, a combination of normal dose and low-dose scan protocols will be employed (e.g., normal dose on supine, low-dose on prone), low-dose CTC based on the low-dose CT scanning protocol and an artifacts reduction technique will be introduced to reduce the radiation risk in screening.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polyps, Colorectal Neoplasm

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CT colonoscopy(normal dose)
Arm Type
Active Comparator
Arm Description
Perform CT colonoscopy with full bowel preparation and inflated colon, CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kilovolts peak (kVp), 100-200mA
Arm Title
CT colonoscopy(low dose)
Arm Type
Experimental
Arm Description
Perform CT colonoscopy with full bowel preparation and inflated colon, CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kVp, 20-100mA
Intervention Type
Radiation
Intervention Name(s)
CT colonoscopy(normal dose)
Intervention Description
Perform CT colonoscopy with full bowel preparation and inflated colon,CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kVp, 100-200mA
Intervention Type
Radiation
Intervention Name(s)
CT colonoscopy (low dose)
Intervention Description
Perform CT colonoscopy with full bowel preparation and inflated colon,CT Scans on subjects with normal-dose protocol by setting scanning parameters as 120-140 kVp, 20-100mA
Primary Outcome Measure Information:
Title
Sensitivity and specificity of low-dose CTC for the polyp detection
Description
return the number of polyps detected by low-dose CTC for each participant, sensitivity and specificity of low-dose CTC for the polyp detection can be derive from it with OC results as reference.
Time Frame
within the first 30 days (plus or minus 3 days) after the completion of the first part of the trial
Secondary Outcome Measure Information:
Title
CT radiation
Description
Record the dose-length product of each CT scan for CTC participants and radiation dose of each scan can be derived from it.
Time Frame
within the first 3 days after each examination.
Title
Sensitivity and specificity of CTC for the detection of polyps with different shapes
Description
Return the shape and location information of polyps detected by OC and CTC for each participant to reflect the CTC performance for the detection of polyps with different morphologies, especially for three major morphologic categories: sessile, pedunculated, and flat.
Time Frame
within the first 30 days after the completion of the trial.
Title
Sensitivity and specificity of CTC for the detection of poly malignancy
Description
Return the histological types of polyps biopsied through OC after pathologic examination to reflect the CTC performance for the detection of polyp malignancy, especially the capability to differentiate adenomatous polyps from hyperplastic polyps.
Time Frame
within the first 30 days after the completion of the trial.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects with gastrointestinal symptoms potentially suggestive of colorectal cancer, such as diarrhea, constipation, abdominal pain or discomfort, rectal bleeding, iron-deficiency anemia, and unintended weight loss. Subjects with pathological confirmed colorectal cancer or polyps that need follow-up examination. Subjects with written consents Exclusion Criteria: Subjects with acute colitis Acute diverticulitis Inguinal hernia including colon Colorectal surgery or endoscopic biopsy or resection of polyps within 6 months Known or suspected as colon perforated Complete intestinal obstruction Pregnant or lactating women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shuhui Liang, MD
Email
liangsh@fmmu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shuhui Liang, MD
Organizational Affiliation
Air Force Military Medical University, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jiang Meng, MS
Organizational Affiliation
Air Force Military Medical University, China
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xiaofeng Zhang, MD
Organizational Affiliation
Air Force Military Medical University, China
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hong Yin, MD
Organizational Affiliation
Air Force Military Medical University, China
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hainan Sang, MS
Organizational Affiliation
Air Force Military Medical University, China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xi jing Hospital
City
Xi'an
State/Province
Shan XI
ZIP/Postal Code
710032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liang Shuhui, MD
First Name & Middle Initial & Last Name & Degree
Sang Hainan, MS

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Colorectal Polyps Screening With Low-dose CT Colonoscopy

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