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Clinical Trials/NCT03167476
NCT03167476
Unknown
Not Applicable

Comparative Study of microRNA Changes in Patients With Reactive Lymphoid Hyperplasia and Malignant Lymphoma

University of Electronic Science and Technology of China1 site in 1 country200 target enrollmentAugust 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lymphoma
Sponsor
University of Electronic Science and Technology of China
Enrollment
200
Locations
1
Primary Endpoint
The concentration of miRNA expression quantitated in absolute copy numbers and their correlation in patients with reactive hyperplasia and lymphoma.
Last Updated
8 years ago

Overview

Brief Summary

The objectives are to:

  1. validate a panel of tissue-specific miRNAs that are differentially expressed in the tissue of patients with and without reactive hyperplasia and lymphoma.
  2. investigate the physiological range of the miRNA panel in lymphoma and reactive hyperplasia subjects.
  3. investigate the dysregulation of miRNA panel and their prognostic and predictive values in clinical outcomes to identifying patients with malignant lymphoma or reactive hyperplasia.

The objectives are to:

  1. validate a panel of tissue-specific miRNAs that are differentially expressed in the tissue of patients with and without reactive hyperplasia and lymphoma.
  2. investigate the physiological range of the miRNA panel in lymphoma and reactive hyperplasia subjects.
  3. investigate the dysregulation of miRNA panel and their prognostic and predictive values in clinical outcomes to identifying patients with malignant lymphoma or reactive hyperplasia.

This trial involves tissue samples diagnosed as lymphoma and reactive hyperplasia. The investigators will develop panels of miRNAs that are specific biomarkers of lymphoma, and assist clinical outcomes with these miRNAs.

Registry
clinicaltrials.gov
Start Date
August 1, 2016
End Date
December 1, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Electronic Science and Technology of China
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults 18 years and above
  • Has condition related to lymphoma or reactive lymphoid hyperplasia

Exclusion Criteria

  • Age below 18 years
  • Known pregnancy
  • lymph tissue cannot be accessed

Outcomes

Primary Outcomes

The concentration of miRNA expression quantitated in absolute copy numbers and their correlation in patients with reactive hyperplasia and lymphoma.

Time Frame: Three years

The concentration of tissue miRNAs in absolute quantification in comparison to reactive hyperplasia and lymphoma. To investigate the potential prognosis of lymphoma by the expression difference of the miRNA panel. Sensitivity, specificity and the potential scopes of selected miRNA in the miRNA panel to distinguish hyperplasia and lymphoma and against standard clinical outcome.

Study Sites (1)

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