se of the oral sialogogue, oryza tablet, in reducing drug-induced xerostomia in patients with overactive bladder or neurogenic bladder: randomized clinical study
Phase 3
Completed
- Conditions
- Xerostomia in patients with overactive &neurogenic bladder receiving antimuscarinic drugsxerostomia, overactive bladder, OAB, neurogenic bladder
- Registration Number
- TCTR20240715015
- Brief Summary
Continuous daily use of Oryza tablet for 4 weeks reduced xerostomia symptoms and increased saliva production in patients suffering from neurologic bladder or overactive bladder who received antimuscarinic medications.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
Overactive bladder and neurogenic bladder patient who use anticholinergic drug with xerostomia symptoms
Age 18 year old or older
Informed consent was made
Exclusion Criteria
Recently xerostomia symptoms within 3 months
History of head & neck radiation
Autoimmune disease
History of salivary gland surgery
Dental and oral infection
Uncooperative patient
History of drug allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Xerostomia symptoms 1 month Subjective dry mouth VAS
- Secondary Outcome Measures
Name Time Method Stimulated salivary flow rate 1 month Prohibited from eating and drinking for 60 mins before saliva collection. They chewed a paraffin cube for 30 seconds, then spit into a tube for 5 mis, after which the saliva volume was measured.