Gastric Tumor Clinical Trial
Official title:
Flexible Endoscopy Biopsies With the New Drill Biopsy Instrument for Submucous Tumors
NCT number | NCT02161029 |
Other study ID # | 2014/97 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 2, 2014 |
Est. completion date | March 27, 2015 |
Verified date | January 2019 |
Source | Region Skane |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine whether the newly constructed CE (Conformité Européenne) marked drill biopsy instrument for flexible endoscopes can make possible representative biopsies of the increasing numbers of submucosal tumours in the gastrointestinal tract. The amount of submucous tissue ( micrograms and in % of all the biopsy) harvested with the new drill biopsy instrument used in flexible endoscopy investigations is measured in the study and compared to the amount of submucous tissue harvested with the existing biopsy forceps.
Status | Completed |
Enrollment | 10 |
Est. completion date | March 27, 2015 |
Est. primary completion date | March 27, 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Submucous gastrointestinal tumours Exclusion Criteria: - No gastrointestinal submucous tumor - Submucosal hemangioma |
Country | Name | City | State |
---|---|---|---|
Sweden | Department of Surgery, Lund University | Lund |
Lead Sponsor | Collaborator |
---|---|
Region Skane | Lund University, Lund University Hospital |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Amount of submucous tissue in gastrointestinal submucosal tumors harvested with a new drill biopsy instrument used with flexible endoscopes. | Amount of submucous tissue adequate for histological examination harvested with the new drill biopsy instrument for flexible endoscopy and compared to the amount harvested with the existing biopsy forceps in a randomized setting. | Within 30 days for each patient |
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