Clinical research for relationship between serum IL-31 and pruritus in patients who undergo hemodialysis
Not Applicable
Completed
- Conditions
- hemodialysis
- Registration Number
- JPRN-jRCT1080224513
- Lead Sponsor
- Chugai Pharmaceutical Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Personally provided written informed consent for the clinical study and able to comply with the requirements of the study protocol
- Aged =>20 and <75 years old at the time of informed consent
- Has undergone hemodialysis (including hemodiafiltration) 3 times a week for at least 12 weeks before enrollment
Exclusion Criteria
- Deemed unsuitable as a subject in the study by the investigator for some other reason
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method