Evaluation of the effectiveness of Xerolacer artificial saliva in relieving the symptoms of patients with dry mouth after radiotherapy in the head and neck regio
Not Applicable
- Conditions
- Changes in salivary secretion
- Registration Number
- RBR-5q6h4qb
- Lead Sponsor
- Faculdade de Odontologia da Universidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients with radioinduced xerostomia.
Exclusion Criteria
Patients with normal salivary flow; patients who do not wish to participate in the study; under 18 years of age; pregnant women; lactating;
illiterate; incapable.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method