New method for detecting MicroRNA in breast cancer patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on developing a novel in-situ detection method for MicroRNA in the serum of patients diagnosed with breast cancer. The approach aims to improve the accuracy of MicroRNA detection, which could enhance the understanding of breast cancer progression and treatment response. By analyzing serum samples, the study seeks to establish a reliable biomarker for monitoring the disease. The methodology involves collecting serum samples from participants and applying the new detection technique to assess MicroRNA levels.

Why it matters

Who can join: the full rules

Inclusion Criteria: Healthy without serious diseases

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Exclusion Criteria:

* situations that may affect the results

Where it's running

• Tongji Hospital
  Wuhan, Hubei, China Recruiting

Study contacts

• Study coordinator: Lei Dou, Dr.
• Email: 616732045@qq.com
• Phone: 15171473498

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.