Clinical Relevance of the Salvage Treatment for Colorectal Neuroendocrine Tumors
NCT ID: NCT06143605
Last Updated: 2023-11-22
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.
COMPLETED
527 participants
OBSERVATIONAL
2013-01-30
2023-09-30
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.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
salvage treatment group
patients with salvage treatment after endoscopic resection were diagnosed as having positive resection margin status
salvage treatment
salvage radical surgery or endoscopic resection
without salvage treatment group
patients without salvage treatment after endoscopic resection were diagnosed as having positive resection margin status
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
salvage treatment
salvage radical surgery or endoscopic resection
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yanhong Deng
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yanhong Deng
M.D.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
GIH-SYip33
Identifier Type: -
Identifier Source: org_study_id