Effectiveness of Artificial Saliva in improving dry mouth and quality of life among the elderly
Phase 2
- Conditions
- Health Condition 1: K110- Atrophy of salivary gland
- Registration Number
- CTRI/2021/01/030436
- Lead Sponsor
- ot applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adults aged >=60 years, who are under at least 2 prescription medications for a year or more and unstimulated salivary flow rate <= 0.25 ml/min
Exclusion Criteria
Patients with a history of Sjogrenâ??s syndrome, Salivary gland infection, Irradiated Head and neck cancer patients,
History of total or partial removal of Salivary glands,
Participant who is not willing to sign the informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method XerostomiaTimepoint: 2 months after intervention
- Secondary Outcome Measures
Name Time Method oral health related quality of lifeTimepoint: 2 months after intervention