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Clinical Trials/NCT06155539
NCT06155539
Not yet recruiting
Not Applicable

A Study of Blood Metabolic Markers in Patients With Type 2 Diabetes Mellitus of Different Stages

Peng Wu1 site in 1 country105 target enrollmentJanuary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
Peng Wu
Enrollment
105
Locations
1
Primary Endpoint
Differential metabolites
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

Metabolomics is an emerging "omics" after genomics, transcriptomics and proteomics, which can reflect the physiological state of organisms more directly and accurately. Whether metabolite differences exist in patients with type 2 diabetes of different stages and whether such metabolite differences can be used as potential markers have not yet been studied, which is of great significance to explore. In this study, 105 patients with different stages of type 2 diabetes mellitus were enrolled according to the inclusion and exclusion criteria, and the metabolites in the samples were detected by ultra-high performance liquid chromatography coupled with tandem time-of-flight mass spectrometry (UHPLC-Q-TOF MS) after the blood samples were collected, and the corresponding investigative data were collected, and then baseline and demographic analyses, metabolomics data processing, and analysis of the results were carried out to provide a reference for the identification of metabolic markers and to provide a reference for the identification of significant metabolic markers in diabetic patients.

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
December 31, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Peng Wu
Responsible Party
Sponsor Investigator
Principal Investigator

Peng Wu

professor

Qianfoshan Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18 to 75 years old
  • Population of patients with type 2 diabetes mellitus of different stages
  • Subjects or legal representatives gave informed consent to voluntarily join the study by signing an informed consent form.

Exclusion Criteria

  • patients with severe acute underlying brain, cardiac, pulmonary, hepatic, renal and other conditions that the investigator believes to be influential
  • Patients diagnosed with any malignancy within the previous 5 years;
  • Received any form of oncological treatment including surgery, radiotherapy/chemotherapy, endocrine therapy, targeted therapy and immunotherapy prior to entry for blood sampling;
  • Organ transplant recipients or previous non-autologous (allogeneic) bone marrow or stem cell transplant recipients;
  • Those who have received blood transfusion therapy 1 month prior to the blood draw;
  • Patients with blood-borne diseases such as hepatitis, syphilis, and HIV;
  • Patients with other factors that, in the opinion of the investigator, influence the study.

Outcomes

Primary Outcomes

Differential metabolites

Time Frame: 2024.01-2025.12

Study Sites (1)

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