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Clinical Trials/ITMCTR2200006534
ITMCTR2200006534
Not yet recruiting
Phase 3

Clinical evidence-based evaluation of Traditional Chinese Medicine for prevention and treatment of diabetic high-risk foot

Hospital of Chengdu University of TCM0 sitesTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
High risk foot of diabetes
Sponsor
Hospital of Chengdu University of TCM
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Hospital of Chengdu University of TCM

Eligibility Criteria

Inclusion Criteria

  • 1\. Meet the diagnostic criteria for type 2 diabetes defined in the Guideline for the prevention and treatment of type diabetes mellitus in China (2020 edition);
  • 2\.Meet the diagnostic criteria for high\-risk foot for diabetes;
  • 3\.Age between 18 and 80 years old, regardless of gender;
  • 4\.Voluntarily participate in this trial and sign the informed consent.

Exclusion Criteria

  • 1\. Patients with typical diabetic foot symptoms such as foot ulcers, infections, and gangrene;
  • 2\.There are other diseases that cause damage to peripheral nerves and blood vessels;
  • 3\.Mentally ill patients;
  • 4\.Combined with serious heart, brain, kidney and other complications, or combined with other serious primary diseases;
  • 5\.Those who have a history of allergies or allergies to drugs, food, pollen, etc.;
  • 6\.Pregnant, lactating women and women planning to become pregnant;
  • 7\.Those who use hormones and undergo surgical treatment and other stressful states of the body;
  • 8\.Patients with acute diabetic complications such as ketoacidosis and hyperosmolarity and concurrent infections;
  • 9\.Patients who use antioxidant drugs (such as lipoic acid), anti\-platelet aggregation drugs (such as aspirin enteric\-coated tablets), Chinese patent medicines and other nerve and vascular disease prevention drugs and nutritional nerve preparations (such as methylcobalamin);
  • 10\.Those who have participated in other clinical trials within three months.

Outcomes

Primary Outcomes

Not specified

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