Study on the effect of Naldemedine Tosilate by diet
Not Applicable
- Conditions
- opioid-induced constipation
- Registration Number
- JPRN-UMIN000029459
- Lead Sponsor
- ational Hospital Organization Takasaki General Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 14
Inclusion Criteria
Not provided
Exclusion Criteria
1.Performance status(3-4) 2.artificial anus 3.ileus of intestine 4.patients taking specific dietary form (for example,liquid diet,etc) 5.Having regular use of Itraconazole,Fluconazole, Rifampicin,Ciclosporin 6.Patients who do not obtain written consent 7.Patients judged inappropriate by the research director
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of the change amount from the baseline of the number of SBM per week due to the difference in usage and the time from oral administration to the first SBM
- Secondary Outcome Measures
Name Time Method 1) Change amount of NRS score 2) Change in rescue usage 3) Survey of senses by questionnaire