Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions in the Colon Indicative of Ulcerative Colitis Disease

NCT ID: NCT02025777

Last Updated: 2016-03-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-05-31
• Study Completion Date: 2015-06-30

Brief Summary

Study Hypothesis UC Disease affects the colon. PillCam IBD may be used for visualization of the colon mucosa in UC Disease patients. This study is designed to evaluate the yield and clinical impact of IBD capsule in detecting lesions associated with UC Disease and to determine the agreement between PillCam Platform with the IBD capsule and optical colonoscopy in the evaluation of UC disease extent.

Primary Scientific Objective To evaluate the agreement between PillCam IBD system and optical colonoscopy in the evaluation of UC disease extent (Non-active disease, Proctitis, Left-sided colitis, Pancolitis)

Proposed Design Established UC disease patients whose clinical condition suggests ongoing disease activity, aged 18 years and up, who have no evidence of symptomatic stricture or other obstruction that would prevent capsule passage will be enrolled in this study.

Patients will undergo bowel prep, followed by a PillCam IBD capsule examination and colonoscopy examination.

The Rapid videos will be evaluated by two readers, each from a different site, the colonoscopy videos will be evaluated by two other physicians, at the sites

INCLUSION CRITERIA

All subjects must fulfill all of the following inclusion criteria:

• Patients ages 18 years and up
• Patient has known UC according to physician discretion
• Patient has at least one positive inflammatory marker from the following:

• ESR
• CRP
• CBC
• Patient is indicated and eligible for a standard of care colonoscopy examination
• Patient agrees to sign consent form

EXCLUSION CRITERIA

The presence of any of the following will exclude a patient from study enrollment:

• Crohn's Disease
• Antibiotic Associated Colitis
• Stool positive for O&P (C&S within 3 months of enrollment)
• Other known infectious cause of increased symptoms
• Known intestinal obstruction or current obstructive symptoms, such as severe abdominal pain with accompanying nausea or vomiting.
• Definite long stricture seen on radiological exam.
• Non-steroidal anti-inflammatory drugs including Aspirin, (twice weekly or more) during the 4 weeks preceding enrollment
• Suspected GI stricture, followed by patency capsule study or other imaging study that could not prove patency of the GI tract.
• Patient has had prior abdominal surgery of the gastrointestinal tract in the last 6 months, other than uncomplicated procedures that would be unlikely to lead to bowel obstruction based on the clinical judgment of the investigator.
• Patient is expected to undergo MRI examination within 7 days after ingestion of the capsule.
• Patient with known gastrointestinal motility disorders.
• Subjects with known or suspected delayed gastric emptying
• Patient suffers from any condition, such as swallowing problems, which precludes compliance with study and/or device instructions.
• Patient has Type 1 or Type II Diabetes.
• Patient has any allergy or other known contraindication to the medications used in the study.
• Patient has any condition, which precludes compliance with study and/or device instructions.
• Women who are either pregnant or nursing at the time of screening, or are of child-bearing potential and do not practice medically acceptable methods of contraception.
• Concurrent participation in another clinical trial using any investigational drug or device.
• Patient suffers from a life threatening condition
• Patients with history or clinical evidence of renal disease and/or previous clinically significant laboratory abnormalities of renal function parameters.

Conditions

Ulcerative Colitis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

capsule endoscopy and colonoscopy

Group Type: EXPERIMENTAL

Capsule Endoscopy

Intervention Type: DEVICE

Interventions

Capsule Endoscopy

Intervention Type: DEVICE

Other Intervention Names

CE

Eligibility Criteria

Inclusion Criteria

• Patients ages 18 years and up
• Patient has known UC according to physician discretion
• Patient has symptoms of fresh bleeding and/or bloody diarrhea and/or at least one positive inflammatory marker within the past three months from the following:

• ESR
• CRP
• CBC
• Patient is indicated and eligible for a standard of care colonoscopy examination for evaluation of disease activity and not for routine screening for dysplasia or colorectal cancer
• Patient agrees to sign consent form

Exclusion Criteria

• Crohn's Disease
• Antibiotic Associated Colitis
• Stool positive for O&P and for C. difficile toxin within 3 months of enrollment
• Other known infectious cause of increased symptoms
• Known intestinal obstruction or current obstructive symptoms, such as severe abdominal pain with accompanying nausea or vomiting.
• Definite tight or long stricture seen on radiological exam.
• Non-steroidal anti-inflammatory drugs including Aspirin, (twice weekly or more) during the 4 weeks preceding enrollment
• Suspected GI stricture, followed by patency capsule study or other imaging study that could not prove patency of the GI tract.
• Patient has had prior abdominal surgery of the gastrointestinal tract in the last 6 months, other than uncomplicated procedures that would be unlikely to lead to bowel obstruction based on the clinical judgment of the investigator.
• Patient is expected to undergo MRI examination within 7 days after ingestion of the capsule.
• Patient with a known gastrointestinal motility disorder.
• Subjects with known or suspected delayed gastric emptying
• Patient suffers from any condition, such as swallowing problems, which precludes compliance with study and/or device instructions.
• Patient has Type 1 or Type II Diabetes.
• Patient has any allergy or other known contraindication to the medications used in the study.
• Women who are either pregnant or nursing at the time of screening, or are of child-bearing potential and do not practice medically acceptable methods of contraception.
• Concurrent participation in another clinical trial using any investigational drug or device.
• Patient suffers from a life threatening condition
• Patients with history or clinical evidence of renal disease and/or previous clinically significant laboratory abnormalities of renal function parameters.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic - MITG

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yago González Lama, Dr.

Role: PRINCIPAL_INVESTIGATOR

Locations

Sheari-Zedek Medical Center

Jerusalem, , Israel

Puerta de Hierro

Majadahonda, Madrid, , Spain

Countries

Israel; Spain

Other Identifiers

RD-210

Identifier Type: -

Identifier Source: org_study_id