Intervention study of oral dryness - Armor.

Completed

• Conditions: xerostomie; dry mouth sensation; xerostomia

• Registration Number: NL-OMON40736
• Lead Sponsor: VU Medical Centre

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 66

Inclusion Criteria

- Sjögren syndrome patient * diagnosed and / or self-reported
- Reported complaints of dry mouth
- Unstimulated salivary flow <0.20 ml/min

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameter is dry mouth sensation, assessed with the validated<br /><br>Visual Analogue Scale questionnaire and the Xerostomia Inventory.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary objective of this study is to evaluate the overall appreciation<br /><br>of the mouthwash. </p><br>