Effect of nalfurafine hydrochloride in patients with chronic liver disease with refractory pruritus on sleep disorders: A study protocol for prospective interventional study
Not Applicable
- Conditions
- Chronic liver disease patients with refractory pruritus
- Registration Number
- JPRN-UMIN000028161
- Lead Sponsor
- Hyogo college of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
(1)Patients with past history for hypersensitivity for the ingredients of testing drugs. (2)Female patients with pregnancy or suspected of being pregnant, or those desiring pregnancy during study period. (3)Lactating female patients (4)Patients who were judged to be inappropriate for the study subjects
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method