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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03073226
Other study ID # PHT/2015/105
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 6, 2016
Est. completion date February 6, 2018

Study information

Verified date June 2019
Source Portsmouth Hospitals NHS Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Barrett's oesophagus is a condition where the lining of the oesophagus (gullet) wall changes. People with Barrett's oesophagus are at risk of developing oesophageal cancer but can have regular checkups to detect changes before they progress to cancer. Every two years patients with Barrett's are offered examination by passing a fibreoptic tube into the oesophagus (gastroscopy) to remove small tissue samples (biopsies), which are examined in the laboratory to check for changes.

Bowel cancer is the third most common cancer in the UK, and the second leading cause of cancer deaths. Prevention and early detection are the most effective strategies of dealing with bowel cancer. Most cancers develop from benign polyps (growths) in the bowel. Polyps are common and have the potential of developing into cancer over the course of many years.

Patients with a prior diagnosis of Barrett's oesophagus and colonic polyps undergo regular endoscopic examinations known as surveillance endoscopies. This is done to detect changes in the cells of Barrett's oesophagus or further polyps. Current practice is to capture recorded videos of Barrett's surveillance examinations and still images of polyps prior to their removal.

Endoscope technology continues to advance. These newly developed technologies are marketed to have claims of superiority in performance over preceding generations often without the back up of scientific data but at a significant financial cost. The aim of this study is to use endoscopic images and videos recorded as part of routine clinical practice to compare the current version of Olympus endoscopes with the new version launched by the company.


Recruitment information / eligibility

Status Completed
Enrollment 232
Est. completion date February 6, 2018
Est. primary completion date November 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients attending for Barrett's surveillance OR

- Patients attending for colonic polyp surveillance or screening

- Patients are willing and able to give informed consent.

Exclusion Criteria:

- Polyp syndromes (eg FAP or Lynch Syndrome)

- Known history of IBD

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Olympus Elite
New generation Olympus endoscope
Olympus Spectrum
Current generation Olympus endoscope

Locations

Country Name City State
United Kingdom Queen Alexandra Hospital Portsmouth

Sponsors (1)

Lead Sponsor Collaborator
Portsmouth Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity Difference in the sensitivity of in vivo lesion characterisation between Lucera Elite vs Lucera Spectrum as compared to final histology. Baseline and 1 day
Secondary Difference in clarity of images/videos between Lucera Elite and Lucera Spectrum technology. Difference in clarity of images/videos between Lucera Elite and Lucera Spectrum technology. Baseline and 1 day
Secondary Sensitivity of Dual Focus technology Difference in sensitivity of lesion characterisation when using dual focus technology. Baseline and 1 day
Secondary Endoscopists confidence Difference in endoscopists' confidence scores in lesion characterisation between new and current technologies. Baseline and 1 day
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