The Pandemic's Effect on Diagnosis and Treatment of Rectal Cancer
NCT ID: NCT05328960
Last Updated: 2023-12-08
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.
RECRUITING
8000 participants
OBSERVATIONAL
2022-02-15
2025-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The aim of this study is to evaluate the effects of the Covid-19 pandemic on the diagnosis, treatment and survival of patients with colorectal cancer.
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.
Patients diagnosed before, during or after the pandemic
Patients with rectal cancer
Diagnosed during or not during the pandemic
We will create a group of patients that are diagnosed before and after the pandemic and one group diagnosed during the pandemic
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Diagnosed during or not during the pandemic
We will create a group of patients that are diagnosed before and after the pandemic and one group diagnosed during the pandemic
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
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sahlgrenska University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Eva Angenete
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dept. of Surgery, Sahlgrenska University Hospital/Ostra
Gothenburg, , Sweden
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Eva Angenete, MD,PhD
Role: primary
Anette Wedin, RN
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CovidRC
Identifier Type: -
Identifier Source: org_study_id