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Efficacy of prostaglandin E1 (alprostadil alfadex) in hemodialysis patients with peripheral arterial disease (PAD): Examination of the therapeutic effect based on measurement of skin perfusion pressure (SPP)

Not Applicable
Conditions
Peripheral Arterial Disease
Registration Number
JPRN-UMIN000005169
Lead Sponsor
Ikegami General hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients with no symptoms of PAD (cold feeling, sense of numbness, intermittent claudication, pain during rest, etc.) 2. Patients under treatment with PGE1 3. Patients with symptoms of inflammatory, coronary artery, or cerebrovascular disease within the previous 3 months 4. Patients with severe hepatic or cardiac disease 5. Patients under treatment for a malignant tumor or those who had received treatment for a malignant tumor within the previous 5 years 6. Pregnant patients, lactating patients, patients who showed signs of pregnancy, and patients who intended to become pregnant 7. Patients with a history of hypersensitivity to PGE1 injection 8. Other patients who were judged to be inappropriate for the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Amelioration of SPP
Secondary Outcome Measures
NameTimeMethod
Results from a questionnaire survey and a visual analogue scale (VAS) Improvement of subjective symptoms, safety, and changes in blood pressure during hemodialysis
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