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Treatment of refractory ulcers with Simonkolleite

Recruiting
Conditions
refractory skin ulcer
Registration Number
jRCTs021210047
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria
  1. Patients who do not show a healing tendency after 3 weeks or more of existing conservative treatments [ointment treatment, wound dressing, basic fibroblast growth factor (bFGF), continuous negative pressure wound therapy (NPWT) etc.]
  2. Patients who explained the purpose of this study in a separate document and obtained written consent
Exclusion Criteria
  1. Patients with ulcer infection
  2. Patients with refractory skin ulcers caused by artificial objects
  3. Patients with refractory skin ulcers caused by malignant tumors
  4. Patients being treated for malignant tumors
  5. Pregnant patients
  6. Other patients deemed inappropriate by researchers

Study & Design

Study Type
Interventional
Study Design
single assignment
Primary Outcome Measures
NameTimeMethod
-

Detection of adverse findings

Secondary Outcome Measures
NameTimeMethod

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