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Evaluation of palatability of newly developed fast disintegrating tablet of Kremezin in patient.

Not Applicable
Conditions
Chronic renal failure
Registration Number
JPRN-UMIN000031986
Lead Sponsor
School of Pharmaceutical Sciences University of Shizuoka
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who apply to administration contraindications in the package insert of kremezin Patients who will not see the outpatients clinic within 2 weeks to 2 months Patients who can not communicate due to cognitive deterioration Patients who do not manage medication by themselves and their families Patients who it is hard to swallow Patients who have extraordinary state in oral cavity. Patients who is considered as imappropriate by doctor.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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