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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04798976
Other study ID # 20210312
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date May 30, 2021

Study information

Verified date March 2021
Source Center of Personalized Medicine, Pirogova
Contact Evgeny Pokushalov, Prof. MD PhD
Phone 89139254858
Email e.pokushalov@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A population-based case-cohort study of breast cancer-specific survival among all first invasive breast cancer cases


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date May 30, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers No
Gender Female
Age group N/A to 70 Years
Eligibility Inclusion Criteria: All women with stage I-III disease who survived at least 12 months post-diagnosis Exclusion Criteria: Unknown cause of death Treatment outside the region (thus precluding the treatment assessment)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
neoadjuvant/adjuvant therapy
chemotherapy/endocrine therapy/surgery/radiotherapy

Locations

Country Name City State
Russian Federation Evgeny Pokushalov Novosibirsk

Sponsors (3)

Lead Sponsor Collaborator
Center of Personalized Medicine, Pirogova Center for New Medical Technologies, Novosibirsk, Russia., I.M. Sechenov First Moscow State Medical University

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary The percentage of guideline-consistent and personalized EBM recommendations The percentage of guideline-consistent and personalized EBM recommendations acted on by clinicians in patients with first invasive breast cancer. All discrepancies between routine and CDSS-recommended treatment resulting in frame of guideline-consistent therapy and personalized EBM therapy will be adjudicated by core laboratory. 3-year
Secondary Breast cancer-specific survival All deaths due to breast cancer-related causes 3-year
Secondary Quantify the performance of the CDSS (MedicBK) algorithm Quantify the performance of the CDSS (MedicBK) algorithm for presents treatment suggestions in frame of guideline-based therapy and personalized EBM therapy: the sensitivity, specificity, NPV, and PPV 3-year
Secondary Predictors Predictors of guideline-consistent and personalized EBM adherence 3-year