"Underwater" Technique With Submucosal Solution of Viscose Solution -SIC 8000 (EleviewTM) - For Endoscopic Resection of Cole-rectal Polyps With Signs of Fibrosis.
NCT ID: NCT03756636
Last Updated: 2020-01-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2018-06-01
2018-11-26
Brief Summary
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Before the procedure each patient, a normal endoscopic procedure. At the site of the lesion the lumen will be completely decompressed with aspiration of the gas, and then again relaxed with the instillation of only water. The EleviewTM will be injected into the submucosa in such quantities as to obtain a satisfactory lift of the lesion. The lesion will then be removed with a diathermic loop, preferably en-bloc, and in any case up to macroscopic evidence of complete resection. All the removed material will be stored and sent to histological analysis. Tolerability score will be recorded during the procedure.
Any "bleeding" (both intra- and post-procedural), perforation, post-polypectomy syndrome, stenosis or death in the 6 months following the procedure will be born "complication".
A surveillance colonoscopy including biopsy sampling of the research site scheduled 6 months after the procedure
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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"Underwater" mucosectomy
"Underwater" mucosectomy with submucosal injection of viscous solution -SIC 8000 (EleviewTM)
"Underwater" mucosectomy with submucosal injection of viscous solution -SIC 8000 (EleviewTM)
"Underwater" mucosectomy with submucosal injection of viscous solution -SIC 8000 (EleviewTM)
Interventions
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"Underwater" mucosectomy with submucosal injection of viscous solution -SIC 8000 (EleviewTM)
"Underwater" mucosectomy with submucosal injection of viscous solution -SIC 8000 (EleviewTM)
Eligibility Criteria
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Inclusion Criteria
* Signing of informed consent.
* Possibility of being subjected to the diagnostic and therapeutic procedures of the study.
* Presence of colo-rectal polypoid lesions ≥ 15mm presenting macroscopic aspects of fibrosis as a consequence of previous incomplete treatments or biopsies or relapses after previous removal.
Exclusion Criteria
* Pregnancy or breastfeeding
* ASA\> 3
* Unstable personality or unable to adhere to the protocol procedures.
* Inability to provide informed consent.
* Injury not reachable endoscopically.
18 Years
ALL
No
Sponsors
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Istituto Clinico Humanitas
OTHER
Responsible Party
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Locations
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Endoscopy Unit, Gastroenterology Department, Humanitas Research Hospital
Rozzano, Milano, Italy
Countries
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Other Identifiers
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2046
Identifier Type: -
Identifier Source: org_study_id
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