Comparison Between HD+ Endoscopy and Standard Videoendoscopy in Screening Colonoscopy
NCT ID: NCT00792649
Last Updated: 2008-11-18
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
200 participants
OBSERVATIONAL
2008-02-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
screening colonoscopy with HD+ endoscopes
No interventions assigned to this group
2
screening colonoscopy with standardvideoendoscopes
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Cancer
* Pregnancy
* Inability to obtain informed consent
* Prothrombin time \< 50% of control
* Partial thromboplastin time \> 50 seconds
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Johannes Gutenberg University Mainz
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hoffman Arthur
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
837.386.07
Identifier Type: -
Identifier Source: org_study_id