Adenoma Detection Rate Clinical Trial
— EndocuffOfficial title:
A Prospective Randomized Comparison of the Adenoma Detection Rate in Screening Colonoscopy With and Without a Disposable Cap (ENDOCUFF VISION®)
Verified date | June 2023 |
Source | Universitätsklinikum Hamburg-Eppendorf |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study is to evaluate the effect of ENDOCUFF VISION® (caps with soft, about 1 cm long lateral feet of rubber ("Endocuff") to flatten the colon folds) on ADR in a real-life setting (general practices) and in a homogenous patient collective (screening colonoscopies only). It is a prospective randomized multi centric study, with participation of at least 10 study sites (private practice). The study is an inverstigator-initiated trial (IIT). Depending on the randomization (closed envelope), the patients are examined with the standard instruments without or with ENDOCUFF VISION®. Group 1: screening colonoscopy with standard colonoscopes with ENDOCUFF VISION® Group 2: screening colonoscopy with standard colonoscopes without cap
Status | Completed |
Enrollment | 1382 |
Est. completion date | September 30, 2022 |
Est. primary completion date | September 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 55 Years and older |
Eligibility | Inclusion Criteria: - > 55 years - who voluntarily undergo a screening colonoscopy - information and signed declaration of consent Exclusion Criteria: - symptoms that may indicate a colonic disease - rectal/colonic bleeding - known colon disease for further diagnosis, e.g. Carcinoma, polyps for erosion, inflammatory bowel disease, stenosis - follow-up/surveillance after colon carcinoma surgery or polypectomy - anticoagulant drugs that make a biopsy or polypectomy impossible - poor general condition (from ASA (American Society of Anesthesiologists Classification) III) - partial/incomplete colonoscopy planned |
Country | Name | City | State |
---|---|---|---|
Germany | Gastroenterologie am Bayerischen Platz | Berlin | |
Germany | Gastroenterologische Spezialpraxis am Wittenbergplatz | Berlin | |
Germany | Gemeinschaftspraxis Hohenzollerndamm | Berlin | |
Germany | Praxis Dr. Mayr | Berlin | |
Germany | Praxis Dr. med. Jens Aschenbeck | Berlin | |
Germany | Praxis für Gastroenterologie in Berlin Reinickendorf | Berlin | |
Germany | Gastropraxis Eppendorfer Baum | Hamburg | |
Germany | Magen-Darm-Zentrum, Facharztzentrum Eppendorf | Hamburg | |
Germany | Schwerpunktpraxis CCB Bergedorf | Hamburg |
Lead Sponsor | Collaborator |
---|---|
Universitätsklinikum Hamburg-Eppendorf | Norgine |
Germany,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Adenoma Detection Rate (ADR) in the two study groups | Differences in ADR with or without the new disposable ENDOCUFF VISION® cap. Hypothesis: Endocuff Vision improves the adenoma detection rate (ADR) by about 25% compared to the comparison group. | through study completion, an average of 1 year | |
Secondary | ADR (all adenoma/all patients) | ADR (all adenoma/all patients) | 12 months | |
Secondary | assessment of adenoma subgroups by location | differences in adenoma subgroups (between intestinal folds with good accessibility, between intestinal folds with poor accessibility, on top of intestinal fold, behind intestinal fold ) | 12 months | |
Secondary | assessment of adenoma subgroups by size | measured by comparison with size of snare or forceps | 12 months | |
Secondary | assessment of adenoma subgroups by form | stem-based, broad-based, flat adenoma | 12 months | |
Secondary | assessment of adenoma subgroups by histology | loiw grade intraepithelial neoplasia (LGIN), high grade intraepithelial neoplasia (HGIN), sessile serrated Adenoma (SSA), Carcinoma | 12 months | |
Secondary | assessment of adenoma subgroups by adjustability | adjustability of adenoma by colonoscope on a score scale from 1(very good) - 6 (poor) | 12 months | |
Secondary | assessment of adenoma subgroups by resection practice | resection of adenoma by biopsy, polypectomy, resection by forceps, none | 12 months | |
Secondary | Intervention times | duration of Intervention | through study completion, an average of 1 year | |
Secondary | procedure technique | technical aspects of polypectomy/biopsy | through study completion, an average of 1 year |
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