MACCS: Multicenter Australian CE in Patients With Suspected Crohn's Disease Study (MACCS)

Evaluation of Capsule Endoscopy in Patients With Suspected Small Bowel Crohn's Disease

This is a prospective study aimed to validate the ability of capsule endoscopy to accurately diagnose small bowel Crohn's disease in symptomatic patients who have a non-diagnostic standard workup. Patients will be randomized to undergo capsule endoscopy either one week or five weeks after enrolment. Patients will be followed up for up to 3 months after capsule endoscopy.

Study Overview

• Status: Completed
• Conditions: Inflammatory Bowel Diseases

Detailed Description

In the past few years, capsule endoscopy has sparked renewed interest in the investigation of small bowel Crohn's disease. A PillCam™SB capsule (Given Imaging Ltd, Yoqneam, Israel) is an ingestible, disposable video camera that transmits high quality images of the small intestinal mucosa. This enables the small intestine to be readily accessible to physicians investigating for the presence of small bowel disorders such as Crohn's disease. It has been demonstrated that capsule endoscopy identifies Crohn's disease when other methods are not helpful. Diagnostic yields of 70% have been reported in small series of studies performed in suspected small bowel Crohn's disease.

This study is designed to determine the accuracy and clinical impact of Capsule Endoscopy in detecting suspected small Bowel Crohn's Disease whose initial evaluation was non-diagnostic. It will also serve to better understand the impact of capsule endoscopy on the natural history of the disorder.

Patients will be randomized to undergo capsule endoscopy either one week or five weeks after enrolment. This will allow assessment of the natural history of this form of Crohn's disease and ensure that any changes in CDAI and QOL after capsule endoscopy are not merely a result of this natural history.

• Study Type: Observational
• Enrollment (Actual): 119

Contacts and Locations

Study Locations

• Australia
  • New South Wales
    • Camperdown, New South Wales, Australia, 2050
      • Royal Prince Alfred Hospital
  • Queensland
    • Herston, Queensland, Australia, 4029
      • Royal Brisbane and Women's Hospital
  • South Australia
    • Daw Park, South Australia, Australia, 5041
      • Repatriation General Hospital
  • Victoria
    • Box Hill, Victoria, Australia, 3128
      • Eastern Health
    • Fitzroy, Victoria, Australia, 3065
      • St. Vincent's Hospital Melbourne
    • Malvern, Victoria, Australia, 3144
      • Cabrini Medical Centre
    • Parkville, Victoria, Australia, 3050
      • Royal Melbourne Hospital
  • Western Australia
    • Nedlands, Western Australia, Australia, 6009
      • Sir Charles Gardiner Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 10 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

clinics

Description

Inclusion Criteria:

• Patient will be 10 years and older
• Patient suffers from abdominal pain and/or diarrhea for the last 6 weeks and/or expresses extra-intestinal manifestations of CD

• Patient has at least one of the following over the preceding 6 months (plus symptoms suspicious of small bowel Crohn's Disease):

  • Positive inflammatory marker (ESR, CRP, thrombocytosis, leucocytosis, fecal lactoferrin, fecal α-1 antitrypsin)
  • Unexplained anemia,
  • Recurrent fever,
  • Weight loss (at least 10% of normal body weight in adults),
  • Hypoalbuminaemia (<3.5 g/dL),
  • Gastro-intestinal bleeding,
  • Chronic perianal disease (fistula, fissure),
  • Abnormal white cell scan
  • Positive ASCA
  • First degree relative of a person suffering from IBD (only for subjects without known IBD),

• Patient underwent standard evaluation that includes colonoscopy and attempted ileoscopy and also SBFT within six months prior to enrollment, which were non-diagnostic. Blood tests should have been done within one month of enrolment.

  • Patient or legal guardian agrees to sign the Informed Consent Form

Exclusion Criteria:

• Patients with indeterminate colitis where the purpose is only to make a definitive diagnosis and where the inclusion criteria are not otherwise met
• Patient is known to suffer from intestinal obstruction (symptoms such as severe abdominal pain with accompanying nausea or vomiting)
• Definite stricture seen on SBFT
• Patient had suspected GI stricture, a Given® Patency capsule was administered and Patient did not pass the Patency capsule.
• Patient has a pacemaker or other implanted electro-medical device
• Patient has known history of small bowel Crohn's disease
• Patient on treatment for active IBD
• Patient with suspected celiac disease that has not been excluded
• Patient on non-steroidal anti-inflammatory drugs including Aspirin, (twice weekly or higher) during the 3 months preceding enrolment
• Patient is pregnant
• Patient has any condition, which precludes compliance with study and/or device instructions, such as swallowing problems
• Patient suffers from life threatening conditions
• Patient is currently participating in another clinical study that may directly or indirectly affect the results of this study

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort
1; Patients with suspected Crohn's disease

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
• To evaluate the yield of capsule endoscopy for the diagnosis of small bowel Crohn's disease in symptomatic patients with non-diagnostic standard work-up.	end of study

Secondary Outcome Measures

Outcome Measure	Time Frame
• To assess the clinical impact made by CE in patients with clinically suspected small bowel Crohn's disease	end of study

Collaborators and Investigators

• Sponsor: Medtronic - MITG
• Investigators: Principal Investigator: Warwick Selby, MD, Royal Prince Alfred Hospital, Sydney, Australia

Study record dates

Study Major Dates

• Study Start: February 1, 2005
• Primary Completion (Actual): December 1, 2007
• Study Completion (Actual): February 1, 2008

Study Registration Dates

• First Submitted: February 11, 2007
• First Submitted That Met QC Criteria: February 12, 2007
• First Posted (Estimate): February 13, 2007

Study Record Updates

• Last Update Posted (Actual): July 31, 2019
• Last Update Submitted That Met QC Criteria: July 29, 2019
• Last Verified: February 1, 2007

More Information

Terms related to this study

• Keywords: capsule endoscopy; Patients with suspected small bowel Crohn's disease; small bowel Crohn's disease; PillCam SB
• Additional Relevant MeSH Terms: Digestive System Diseases; Gastrointestinal Diseases; Gastroenteritis; Intestinal Diseases; Inflammatory Bowel Diseases; Crohn Disease
• Other Study ID Numbers: MA-36