Intervention study of oral dryness - Armor.

Intervention study of oral dryness - Armor. - Isoda

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON40736

Enrollment

Registered

2014-11-11

Start date

2014-11-18

Completion date

Unknown

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

xerostomie dry mouth sensation xerostomia

Interventions

During the intervention a random selection of half of the group of Sjögren patients will be requested to rinse two times a daily with 15 ml mouthwash for one minute . The other half of the group of

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Sjögren syndrome patient * diagnosed and / or self-reported - Reported complaints of dry mouth - Unstimulated salivary flow

Exclusion criteria

Exclusion criteria: - Medication affecting taste or salivary flow - Head and neck radiated therapies - Unstimulated salivary flow > 0.20 ml/min - No computer / e-mail / not familiar or capable using the online web site

Design outcomes

Primary

Measure	Time frame
The main study parameter is dry mouth sensation, assessed with the validated Visual Analogue Scale questionnaire and the Xerostomia Inventory.	—

Secondary

Measure	Time frame
The secondary objective of this study is to evaluate the overall appreciation of the mouthwash.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)