Z-103 Phase III Clinical Study in patients with Taste Disorder - A placebo-controlled superiority study
Phase 3
- Conditions
- taste disorders induced by zinc-deficiency
- Registration Number
- JPRN-jRCT2080221862
- Lead Sponsor
- Zeria Pharmaceutical Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Sex
- All
- Target Recruitment
- 260
Inclusion Criteria
Patients diagnosed with the following three types.
1. Zinc-deficient taste disorder
2. Idiopathic taste disorder
3. Drug-induced taste disorder (with some exceptions)
Exclusion Criteria
1. Central nervous system disorder
2. Peripheral neuropathy
3. Intraoral defect and salivary gland disorder
4. Psychiatric disorder
5. Systemic disorders that cause taste disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Final overall efficacy evaluation<br>Filter-paper Disk Method
- Secondary Outcome Measures
Name Time Method Efficacy evaluation at each evaluation period<br>Filter-paper Disk Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Z-103's efficacy in treating zinc-deficiency-induced taste disorders?
How does Z-103 compare to standard-of-care zinc supplementation in taste disorder treatment outcomes?
Are there specific biomarkers that predict patient response to Z-103 in taste disorder trials?
What adverse events are associated with Z-103 treatment for zinc-deficiency-induced taste disorders?
What are the potential combination therapies or competitor drugs for zinc-deficiency-related taste disorders?