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Colonoscopic surveillance using narrow-band imaging in patients with hyperplastic polyposis syndrome (HPS)

Colonoscopic surveillance using narrow-band imaging in patients with hyperplastic polyposis syndrome (HPS)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28466
Enrollment
22
Registered
2008-09-01
Start date
2007-09-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Hyperplastic polyposis syndrome, hyperplastic polyp

Interventions

Patients with HPS will be evaluated by colonoscopy using a prototype endoscopic imaging system which integrates WLE and NBI in one unit (Spectrum system, Olympus, Tokyo, Japan). All segments of the co

Sponsors

Academic Medical Center (AMC), Department of Gastroenterology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients presenting, or under surveillance at the Endoscopy Department of the AMC with: 1. >10 HPs found at colonoscopy, or 2. >5 HPs proximal to the sigmoid colon, or 3. Any number of HPs occurring proximal to sigmoid colon in an individual who has a first-degree relative with HPS.

Exclusion criteria

Exclusion criteria: Exclusion criteria are 1. History of inflammatory bowel disease, 2. Severe coagulopathy, 3. Age less than 18 years and 4. Insufficient bowel preparation (<90% of colonic mucosa visible).

Design outcomes

Secondary

MeasureTime frame
Furthermore, the surface pit pattern of the detected lesions on NBI will be used to obtain the overall accuracy (representing sensitivity and specificity) of this technique, by using the histological diagnosis as the gold standard diagnosis. Moreover, the prevalence and distribution of HPs, SAs, MPs and adenomas in this patient population will be described

Primary

MeasureTime frame
The sensitivity of WLE will be compared to that of NBI for the detection of polyps and cancer in the colon. The sensitivity of each technique will be calculated as the number of lesions detected during the first inspection, divided by the total number of lesions detected by both inspections.

Contacts

Public ContactK.S. Boparai

Academic Medical Center (AMC), Department of Gastroenterology

k.s.boparai@amc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)