Survival of Patients With a Reduction in the Number of Lymph Nodes in Rectal Cancer After Neoadjuvant Chemoradiotherapy
NCT ID: NCT04456283
Last Updated: 2020-07-02
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
250 participants
OBSERVATIONAL
2019-05-20
2021-07-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Expected results:
Survival rate between patients Complete Pathologic Response with less than 12 LN and 12 or more LN.
To determine the difference in survival between patients with less than 12 LN in complete versus incomplete response.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Relationship Between Lymph Node Ratio and Survival Rate in Preoperative Chemoradiation Rectal Cancer Patients
NCT04096118
Prognostic Significance of Lymph Node Ratio in Rectal Cancer on Overall Survival
NCT05667259
BMI and Lymph Node Count in Colorectal Cancer
NCT06334926
Lateral Nodal Recurrence in Rectal Cancer
NCT04486131
Determining the Optimal Examined Lymph Node for Accurate Staging and Long-term Survival in Rectal Cancer
NCT05572151
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Expected results:
To analyze the survival rate between patients Complete Pathologic Response with less than 12 LN and 12 or more LN. To determine the difference in survival between patients with less than 12 LN in complete versus incomplete response. Demonstrate that patients with complete pathologic response and less than 12 LN have a disease-free survival equal to or better than patients with 12 LN or more.
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.
Incomplete pathological response with less than 12 LN.
Patients with incomplete pathological response after Chemoradiation theraphy for Rectal Cancer and less than 12 lymph nodes
Survival
5 year survival after Chemoradiation theraphy for Rectal Cancer
Incomplete pathological response with 12 or more LN.
Patients with incomplete pathological response after Chemoradiation theraphy for Rectal Cancer and 12 lymph or more nodes
Survival
5 year survival after Chemoradiation theraphy for Rectal Cancer
Complete pathological response with less than 12 LN.
Patients with complete pathological response after Chemoradiation theraphy for Rectal Cancer and less than 12 lymph nodes
Survival
5 year survival after Chemoradiation theraphy for Rectal Cancer
Complete pathological response with 12 or more LN.
Patients with complete pathological response after Chemoradiation theraphy for Rectal Cancer and 12 lymph or more nodes
Survival
5 year survival after Chemoradiation theraphy for Rectal Cancer
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Survival
5 year survival after Chemoradiation theraphy for Rectal Cancer
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
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
SERGIO CARLOS NAHAS
UNKNOWN
CAIO SERGIO NAHAS
UNKNOWN
Ivan Cecconello
UNKNOWN
Ulysses Ribeiro Junior
UNKNOWN
University of Sao Paulo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Leonardo Alfonso Bustamante
Post doctoral fellow
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Medicine School, Sao Paulo University
São Paulo, , Brazil
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
9076078
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.