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Search / Trial NCT06505356

Characterization of Microbiological and Genetic Features in Prostate Cancer and Their Association with Disease Stage

Launched by EDGARAS BURZINSKIS · Jul 14, 2024

Trial Information

Current as of August 20, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

Goal 1: Identify Local Inflammatory Response in Prostate Tissue and Systemic Response in the Blood of Patients with Prostate Cancer Depending on the Stage of the Disease and Evaluate Their Prognostic Value

Objective: To investigate and characterize both local and systemic inflammatory responses in prostate cancer patients at various disease stages.

Approach:

* Local Inflammatory Response: Examine prostate tissue samples to identify markers and levels of inflammation. This involves histological analysis and possibly molecular assays (e.g., PCR, immunohistochemistry).
* Systemic Inflammato...

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age: Male patients aged 18 years and older.
  • 2. Diagnosis: Patients who are suspected of having prostate cancer based on clinical data and standard diagnostic protocols.
  • 3. Disease Stage: Patients at any stage of suspected prostate cancer (localized, locally advanced, or metastatic).
  • 4. Consent: Ability and willingness to provide written informed consent.
  • 5. Clinical Data Availability: Availability of comprehensive clinical data.
  • 6. Sample Provision: Willingness to provide blood and/or tissue samples for genetic and inflammatory marker analysis.
  • Exclusion Criteria:
  • 1. Prior Treatment: Patients who have undergone any prior prostate cancer treatments such as surgery, radiation therapy, or systemic therapies (e.g., hormone therapy, chemotherapy).
  • 2. Other Malignancies: Presence of other concurrent malignancies, except for adequately treated basal cell or squamous cell skin cancer.
  • 3. Severe Comorbidities: Patients with severe or uncontrolled comorbid conditions that could interfere with study participation or data interpretation (e.g., severe cardiovascular, pulmonary, hepatic, or renal diseases).
  • 4. Infection: Active infections or other severe medical conditions that could compromise patient safety or study integrity.
  • 5. Non-compliance: Inability to comply with study procedures, follow-up requirements, or any condition that, in the investigator's opinion, could interfere with study participation.
  • 6. Medication Use: Use of medications that could interfere with the study results, such as immunosuppressive drugs.
  • Additional Considerations:
  • Screening: All potential participants will undergo a screening process to verify eligibility criteria.
  • Confidentiality: Ensure all patient data is handled in accordance with privacy regulations and ethical guidelines.
  • Follow-Up: Participants should be willing to attend regular follow-up visits for ongoing data collection and monitoring of disease progression and treatment response.
  • By setting these criteria, the study aims to create a well-defined patient cohort for evaluating the relationship between genetic and inflammatory markers and prostate cancer aggressiveness.

About Edgaras Burzinskis

Edgaras Burzinskis is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on enhancing patient outcomes, he leads initiatives that emphasize rigorous scientific methodologies and ethical standards. His extensive expertise in clinical operations and strategic planning enables the effective management of trials across various therapeutic areas, fostering collaboration among stakeholders to ensure timely and accurate data collection. Burzinskis is passionate about bridging the gap between research and clinical practice, ultimately contributing to the development of safe and effective treatments.

Locations

Kaunas, , Lithuania

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported