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Active, not recruitingNCT07584213Updated May 13, 2026

The Association Between Blood Routine Parameters and Breast Cancer Prognosis

An observational study in Breast Cancer Invasive, sponsored by Wenjin Yin. Active, not recruiting at 1 site in China. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-13.

Sponsored by Wenjin Yin · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,946
Ages
18 Years and older
Sex
Female
01

Study summary

This is a real-world multicentre study to investigate the association between blood routine parameters combined with clinicopathological characteristics and breast cancer prognosis.

02

Conditions studied

  • Breast Cancer Invasive
03

In context

Lead sponsor

Wenjin Yin is the lead sponsor of 8 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Patients were pathologically diagnosed primary invasive breast cancer from October 2013 to December 2023. They had blood routine results.

Inclusion criteria

  • Aged 18 years or older
  • Pathologically confirmed invasive primary breast cancer

Exclusion criteria

Exclusion Criteria:

  • De novo stage IV breast cancer
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,946 participants (estimated)
Patient registry
No

Groups and cohorts

  • Blood routine test

    breast cancer patients with baseline blood routine results available

    Procedure: blood routine test

Interventions

  • Procedureblood routine test

    blood routine test at baseline

06

What researchers measure

Primary outcomes

  1. Disease-free survival

    Disease-free survival time is defined as the time from the date of radical surgery until the date of the first occurrence of local/regional relapse, distant recurrence, contralateral breast cancer, second malignancy and death from any cause.

    Time frame: From the date of radical surgery until time of event up to 3 years

Secondary outcomes

  1. Recurrence-free survival

    Recurrence-free survival time is defined as the time from the date of radical surgery until the date of the first occurrence of local/regional recurrence, distant recurrence and death from any cause

    Time frame: From the date of radical surgery until time of event up to 3 years

  2. Overall survival

    Overall survival time is defined as the time from the date of radical surgery until death from any cause until death from any cause

    Time frame: From the date of radical surgery until time of event up to 3 years

07

Study locations

1 site
  • Renji Hospital, School of Medicine, Shanghai Jiaotong University
    Shanghai, 200127, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07584213
Lead sponsor
Wenjin Yin
Responsible party
Wenjin Yin (Deputy Chief of Breast Surgery Department, RenJi Hospital) — Sponsor-investigator
First posted
May 13, 2026
Start date
May 1, 2026
Primary completion
May 8, 2026
Completion
May 1, 2027 (estimated)
Last update
May 13, 2026

Study contacts

Wenjin Yin
principal investigator · Renji Hospital,School of Medicine, Shanghai Jiaotong University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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