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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03400657
Other study ID # CSMDT-01
Secondary ID
Status Active, not recruiting
Phase N/A
First received January 2, 2018
Last updated January 9, 2018
Start date November 1, 2017
Est. completion date June 2020

Study information

Verified date January 2018
Source Peking University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a prospective, multicenter, non-interventional, controlled clinical study. Evaluate MDT performance and benefit analysis in patients with advanced gastric or colorectal cancer after MDT discussion under real medical practice.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 484
Est. completion date June 2020
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Histopathological diagnosis of recurrent / metastatic gastric or colorectal cancer.

2. Participate in formal MDT discussions at the Research Center.

3. MDT decision-making at least two subjects involved in treatment.

4. Patient informed consent and signed written consent.

Exclusion Criteria:

1. Early or locally advanced gastric cancer or colorectal cancer.

2. Accept informal MDT discussions.

3. MDT decisions recommend only a single subject for treatment of patients.

4. MDT decisions recommend only palliative patients.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Multi-disciplinary Treatment
due to suggestion of Multi-disciplinary Treatment ,the patients would be suggested to chemotherapy or surgery.

Locations

Country Name City State
China Beijing Cancer Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Secondary Differences in overall survival after performing MDT at center Differences in overall survival after performing MDT at center 1 years