KCT0004454
Terminated
未知
Multicenter, therapeutic use observational study to evaluate the effects of concurrent therapy of Sarpogrelate on symptom improvement in patients with peripheral arterial disease
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Kosin University Gospel Hospital
- Enrollment
- 115
- Status
- Terminated
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients between the ages of 19 and 80
- •2\. First administered or administered for less than three months of Sarpogrelate Hydrochloride to improve ischemic symptoms such as ulcers, pain and coldness caused by chronic arterial obstruction (Berger's disease, obstructive atherosclerosis, diabetic peripheral angiopathy, etc.)
- •3\. Written informed consent by patient or his/her legal representative and agreed to participate in the study approved by the Institutional Review Board or ethics Committee
Exclusion Criteria
- •1\. Overall life expectancy \< 2 year.
- •2\. Any medically documented history of bleeding within a week of participating in the study
- •3\. Persons with diseases that may increase bleeding during the study (Hemophilia, Capillary Placebo, Gastrointestinal Ulcers, Urinary Tract Bleeding, Hemoglobin, Vitreous Hemorrhage, etc.)
- •4\. A female patient who is or may be pregnant
- •5\. Female patients who are or will be breastfeeding during the study period
- •6\. Patients who are not suitable for exercise therapy on their own due to cerebrovascular lesions, spinal diseases, muscle diseases, etc.
- •7\. Patients with severe renal or hepatic disease
Outcomes
Primary Outcomes
Not specified
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