Effect of the Dietary Supplement to Alleviate Dry Mouth.
Prospective, Open-label Study to Evaluate the Effectiveness of Dietary Supplement for Dry Mouth in Relieving Xerostomia in the Community Pharmacy Setting.
1 other identifier
interventional
35
1 country
1
Brief Summary
The goal of this study is to learn if dietary supplement works to improve dry mouth in adults. The main question it aims to answer is:
- Does dietary supplement reduce dry mouth sensation in subjects with dry mouth? Participants will:
- Take dietary supplement every day for 7 days
- Visit the pharmacy at the beginning and the end of the study
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 23, 2026
CompletedFirst Posted
Study publicly available on registry
September 29, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
September 29, 2026
September 1, 2026
2 months
September 23, 2026
September 23, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Change from Baseline in the dry mouth intensity at 7 days
The dry mouth sensation will be evaluated by numeric dryness scale from 0 (no dryness) to 10 (maximum dryness imaginable).
From enrollment to the end of the study at 7 days
Study Arms (1)
Dietary supplement
EXPERIMENTALDietary supplement will be taken daily for 7 days
Interventions
Dietary supplement will be taken daily for 7 days
Eligibility Criteria
You may qualify if:
- Age ≥18 years.
- Presence of subjective xerostomia.
- Score ≥4 on the Numerical Rating Scale for Dryness (NRS, 0-10), established as the cut-off point for clinically relevant xerostomia.
- Result consistent with xerostomia on the Fox Questionnaire.
- Provision of written informed consent.
You may not qualify if:
- Inability to understand or complete the study questionnaires.
- Recent initiation of a specific treatment for xerostomia that may interfere with the evaluation.
- Presence of clinical conditions that, in the investigator's judgment, may interfere with the assessment of the study outcomes.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Lacer S.A.lead
Study Sites (1)
Farmacia Marqueta
Barcelona, Spain
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 23, 2026
First Posted
September 29, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
September 29, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Only data included in the publication will be shared.