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A prospective metabonomic study of peripheral blood and tissue in patients with diabetes foot

A prospective metabonomic study of peripheral blood and tissue in patients with diabetes foot

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087286
Enrollment
Unknown
Registered
2024-07-24
Start date
2024-07-25
Completion date
Unknown
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wagner grading 1-5 for diabetes foot

Interventions

A prospective metabonomic study of peripheral blood and tissue in patients with diabetes foot:Not applicable, this project is an observational trial with no intervention measures

Sponsors

Nanjing Nanyao Pharmaceutical Technology Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Serum samples are sourced from residual samples from clinical testing; The tissue samples are sourced from residual skin tissue samples during clinical surgical procedures; 2) Meet storage requirements, that is, serum samples must be stored at room temperature after collection and centrifuged within 12 hours after collection. Then store it continuously at -60 ? until analysis is conducted; After the collection of organizational samples, they must be stored at -60 ? for 1 hour until analysis is carried out; 3) Patient age = 18 years old, gender not limited; 4) When screening, the body mass index (BMI) is between 18.5-30 kg/m2 (inclusive); 5)Patients with clinically diagnosed diabetes foot.

Exclusion criteria

Exclusion criteria: 1) The serum sample shows coagulation or hemolysis phenomena; 2) Incorrect collection or storage of serum or tissue samples; 3) Screening for hyperthyroidism or hypothyroidism that has not received good treatment; 4) Hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive, and/or Treponema pallidum antibody positive; 5) Patients with major physical diseases such as neurological disorders, traumatic brain injury, cardiovascular and cerebrovascular diseases, and severe liver and kidney dysfunction; 6) Pregnant or lactating women; 7) Merge with other significant medical histories; 8) Currently receiving hormone therapy; 9) Researchers believe that patients with other factors are not suitable to participate in this trial

Design outcomes

Primary

MeasureTime frame
Detecting multiple metabolites in serum;

Secondary

MeasureTime frame
Detecting multiple metabolites in the organization;

Countries

China

Contacts

Public ContactXu Gang

Subei People's Hospital

drxugang@126.com+86 180 5106 1692

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026