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PillCam Colon Capsule Endoscopy for Ulcerative Colitis

PillCam Colon Capsule Endoscopy Versus Conventional Colonoscopy for the Detection of the Severity and Extent of Ulcerative Colitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01467609
Enrollment
20
Registered
2011-11-08
Start date
2009-07-31
Completion date
2010-11-30
Last updated
2011-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative Colitis

Keywords

Pillcam colon capsule endoscopy, conventional colonoscopy, ulcerative colitis, endoscopic manifestation, colonoscopy

Brief summary

Pillcam colon capsule (PCC) endoscopy is a novel strategy tool to inspect colon mucosa. The aim of the present study is to evaluate if PCC endoscopy is able to precisely investigate patients with ulcerative colitis and reach high consistency to conventional colonoscopy.

Detailed description

Symptomatic patients with confirmed ulcerative colitis (UC) were enrolled in this prospective single-center study. No sooner had patients gone through Pillcam colon capsule (PCC) endoscopy solution than they got conventional colonoscopy which is recognized as the gold standard examination technique. The extent of mucosal damage and inflammatory lesions during both modalities were recorded for comparison. In addition, the regimen of bowel preparation, completion rate, colonic cleanliness, compliance or adverse events were analyzed.

Interventions

None listed

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients (aged 18-70) * Ulcerative Colitis history * Suffering from symptoms such as hematochezia, diarrhea or abdominal pain

Exclusion criteria

* Patients with a high risk for capsule retention (such as intestinal diverticula, acute abdominal pain without regular defecation indicating intestinal obstruction or a history of abdominal operation or intestinal reconstructed operation), * Patients allergic to sodium phosphate or polyethylene glycol (PEG) solution, * Patients with a history of Crohn's disease * Patients with serious systematic diseases such as congestive heart failure, renal failure or severe liver disease.

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the accuracy of PCC endoscopy in the survey of ulcerative colitis compared with conventional compared with conventionalthe severity of patients investigated by PCC endoscopy and conventional colonoscopy the extent of evolved lesions extent investigated by PCC endoscopy and conventional colonoscopy the safety of PCC endoscopy course (eg: adverse events during bowel preparation and the course; the completion rate)

Secondary

MeasureTime frameDescription
the gastrointestinal transit time (transit time from ingestion to excretion), cecum arrival time (transit time from ingestion to the cecum), and colon residence time (transit time from the arrival in the cecum to excretion)
clinical data such as age, gender,chief complaint
the Mayo score of each case
the quality of colonic preparation4 grades contain excellent, good, fair and poor

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026