Does Hyaluronic Acid Help Relieve Dry Mouth?
NCT07594184 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2026-05-18
Summary
The goal of this clinical trial is to learn if hyaluronic acid infiltration helps relieve dry mouth symptoms in adults with xerostomia. It will also assess the safety and duration of the treatment's effects.
The main questions it aims to answer are:
1. Does hyaluronic acid improve the sensation of dry mouth?
2. What side effects may occur after treatment?
3. How long does the effect of the treatment last?
4. Are there changes in salivary flow and pH after treatment?
Researchers will compare hyaluronic acid to a placebo (a look-alike substance with no active ingredient) to determine its effectiveness.
Participants will:
Receive submucosal injection of either hyaluronic acid or placebo Visit the clinic once a month for 6 months for follow-up evaluations Not be required to perform any tasks at home
Conditions
- Xerostomia
Interventions
- DEVICE
-
Submucosal infiltration of non reticulated hyaluronic acid
Submucosal infiltration of non reticulated hyaluronic acid will be administered all over the buccal cavity (floor of the mouth, yugal mucosa, lips)
- DEVICE
-
Submucosal infiltration of Placebo
Submucosal infiltration of placebo (Sterile 0.9% Sodium Chloride Solution for Injection) will be administered all over the buccal cavity (floor of the mouth, yugal mucosa, lips)
Sponsors & Collaborators
-
University of Barcelona
lead OTHER
Principal Investigators
-
José López, MD, PhD · University of Barcelona
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-11-11
- Primary Completion
- 2026-11-30
- Completion
- 2026-12-31
Countries
- Spain
Study Locations
More Related Trials
-
The Effect of Peroral Sodium Hyaluronate on the Skin
NCT07065110 ·Status: COMPLETED ·Phase: NA
-
Beneficial Effects of Natural Products on Management of Xerostomia
NCT06217614 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of Oral Rinse for Xerostomia
NCT04289051 ·Status: COMPLETED ·Phase: NA
-
Drug-induced Xerostomia. Evaluation of Malic Acid 1%, Salivary Mucins and Buffering Capacity
NCT01652001 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Efficacy of Manuka Honey Oral Rinse in Treatment of Xerostomia
NCT06240806 ·Status: COMPLETED ·Phase: NA
-
Evaluation of an Electro-stimulator for the Treatment of Xerostomia
NCT00509808 ·Status: COMPLETED ·Phase: PHASE4
-
Intraglandular Treatment With Adipose-derived Mesenchymal Stem Cells in Patients With Xerostomia Due to Sjögren's Disease
NCT06805448 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Topical Hyaluronic Acid and Recurrent Aphthous Stomatitis.
NCT04265001 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Enzymatic-Containing Mouth Spray (Oral7®) on Xerostomia Symptoms, Salivary Flow Rate, and Oral Health-Related Quality of Life in Older Patients
NCT06984848 ·Status: RECRUITING ·Phase: NA
-
Efficacy of a Dietary Supplement (Aqualief®) in Xerostomic Patients
NCT03612414 ·Status: COMPLETED ·Phase: NA
-
Effect of Saliva Substitutes on Dental Hard Tissues in Situ
NCT01165970 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
Xerostomia in Patients With a Life-limiting Condition or Frailty
NCT05506137 ·Status: UNKNOWN ·Phase: PHASE3
-
Study of a Dietary Supplement for Reflux During Sleep
NCT02274636 ·Status: UNKNOWN ·Phase: NA
-
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
NCT00852839 ·Status: COMPLETED ·Phase: PHASE2
-
The Efficacy of Thyme Honey Mouth Rinse on Polypharmacy-induced Xerostomia
NCT06201923 ·Status: COMPLETED ·Phase: PHASE4
-
GUM Hydral Mouthwash vs Placebo in the Management of Hyposalivation.
NCT05103124 ·Status: COMPLETED ·Phase: NA
-
Study of Circular RNA Treatment in Patients With Radiation Induced Xerostomia-1
NCT06714253 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Comparing Over-the-counter Dry Mouth Remedies After Radiation
NCT00595933 ·Status: COMPLETED ·Phase: PHASE1
-
Tolerance and Efficiency of an Intrabuccal Biological Film to Enhance Oral Dryness Sensation: The "PREDELFI" Clinical Pilot Study
NCT04206826 ·Status: COMPLETED ·Phase: NA
-
Improvement of Dry Mouth Sufferers After Using an Experimental Dry Mouth Rinse Compared to a Water Control
NCT04189081 ·Status: COMPLETED ·Phase: NA
-
Blinded Dry Mouth Spray Crossover Study
NCT04608773 ·Status: COMPLETED ·Phase: NA
-
An Evaluation of the Impact of a Single Dose of P-552 on Oral Mucosal Wetness
NCT01369589 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Efficacy of Cevimeline Versus Pilocarpine in the Secretion of Saliva
NCT01690052 ·Status: COMPLETED ·Phase: NA
-
Finger-prick Autologous Blood (FAB) for Use in Dry Mouth
NCT03530735 ·Status: UNKNOWN ·Phase: NA
-
Effect of 0.1% Pilocarpine Mouthwash on Xerostomia
NCT01627626 ·Status: COMPLETED ·Phase: NA