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Clinical Study New Gel for Xerostomia (XEROSTOMIA)

Primary Purpose

XEROSTOMIA

Status
Unknown status
Phase
Phase 1
Locations
Spain
Study Type
Interventional
Intervention
gel xerostomia
gel placebo
Sponsored by
Universidad de Murcia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for XEROSTOMIA focused on measuring dry mouth

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects of both sexes 2. Over 18 years. 3. Adequate cultural level and understanding of the clinical study. 4. Agree to voluntarily participate in the study and give their informed consent in writing 5. Present xerostomia of more than three months of evolution / sialometry less than 0.2ml / 5 min.

Exclusion criteria

The presence of at least one of the following criteria will be grounds for exclusion from the clinical trial:

  1. Presence of health problems that may compromise adherence to the study protocol.
  2. Pregnant or breastfeeding women.
  3. Present hypersensitivity to any component of the product under study.

Sites / Locations

  • Lopez-Jornet PiaRecruiting
  • Lopez-Jornet Pia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

GROUP EXPERIMENTAL

CONTROL GROUP

Arm Description

Gel xerostomia Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night

Gel placebo Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night

Outcomes

Primary Outcome Measures

OHIP 14
Quality of oral life. minimun 0 maximum 56 points. As it gets higher, quality of life decreases
Sialometry
Drenaje
Test Thonsom xerostomy
Xerostomia Inventory. the higher the outcome, quality of life decreases

Secondary Outcome Measures

Full Information

First Posted
November 29, 2019
Last Updated
December 3, 2019
Sponsor
Universidad de Murcia
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1. Study Identification

Unique Protocol Identification Number
NCT04184908
Brief Title
Clinical Study New Gel for Xerostomia
Acronym
XEROSTOMIA
Official Title
Clinical Study to Evaluate the Efectiveness and Tolerability of a New Gel for Xerostomia
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2019 (Actual)
Primary Completion Date
November 2, 2019 (Actual)
Study Completion Date
December 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Murcia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
At present, there is no single consensus protocol for the treatment of oral dryness, although the main objective is to improve the quality of life of patients. Current therapy for the control of xerostomia is based on the following measures: General measures ; review and control of drugs,hydration and dietary advice: The main recommendations are found in the following scheme. Saliva stimulants( Topics and sistemic )The option of using chewing stimuli by chewing gum with non-cariogenic sweeteners helps to improve symptoms. The investigators can also use gustatory stimuli, such as citric acid that is a potent stimulator of salivary secretion. Among the most commonly used pharmacological agents are: pilocarpine, bethanecol, civemiline Saliva substitutes or artificial saliva. Saliva substitutes can provide a moisture retention layer in the oral mucosa and can be administered by liquids, spray, pills or gels. Topical treatments have few adverse effects and improve the quality of life of patients with xerostomia; In addition, they maintain oral health.
Detailed Description
Randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and tolerability in patients with a non-commercialized gel and property of the promoter to treat xerostomia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
XEROSTOMIA
Keywords
dry mouth

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GROUP EXPERIMENTAL
Arm Type
Experimental
Arm Description
Gel xerostomia Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night
Arm Title
CONTROL GROUP
Arm Type
Placebo Comparator
Arm Description
Gel placebo Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night
Intervention Type
Drug
Intervention Name(s)
gel xerostomia
Other Intervention Name(s)
lubricant and remineralizing agents
Intervention Description
Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night
Intervention Type
Other
Intervention Name(s)
gel placebo
Intervention Description
Apply 2-3 cm of the gel on the tongue, gums and oral mucosa, at least three times a day, if necessary it can be applied at night
Primary Outcome Measure Information:
Title
OHIP 14
Description
Quality of oral life. minimun 0 maximum 56 points. As it gets higher, quality of life decreases
Time Frame
1moth
Title
Sialometry
Description
Drenaje
Time Frame
1moth
Title
Test Thonsom xerostomy
Description
Xerostomia Inventory. the higher the outcome, quality of life decreases
Time Frame
1moth

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects of both sexes 2. Over 18 years. 3. Adequate cultural level and understanding of the clinical study. 4. Agree to voluntarily participate in the study and give their informed consent in writing 5. Present xerostomia of more than three months of evolution / sialometry less than 0.2ml / 5 min. Exclusion criteria The presence of at least one of the following criteria will be grounds for exclusion from the clinical trial: Presence of health problems that may compromise adherence to the study protocol. Pregnant or breastfeeding women. Present hypersensitivity to any component of the product under study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pia López-Jornet, PhD
Phone
639473308
Email
majornet@um.es
Facility Information:
Facility Name
Lopez-Jornet Pia
City
Murcia
State/Province
N/A = Not Applicable
ZIP/Postal Code
30008
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lopez-Jornet Pia
Phone
639473308
Email
majornet@um.es
Facility Name
Lopez-Jornet Pia
City
Murcia
State/Province
N/A = Not Applicable
ZIP/Postal Code
30008
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lopez-Jornet Pia
Phone
639473308
Email
majornet@um.es

12. IPD Sharing Statement

Citations:
PubMed Identifier
30923424
Citation
Assery MKA. Efficacy of Artificial Salivary Substitutes in Treatment of Xerostomia: A Systematic Review. J Pharm Bioallied Sci. 2019 Feb;11(Suppl 1):S1-S12. doi: 10.4103/jpbs.JPBS_220_18.
Results Reference
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PubMed Identifier
27031061
Citation
Gil-Montoya JA, Silvestre FJ, Barrios R, Silvestre-Rangil J. Treatment of xerostomia and hyposalivation in the elderly: A systematic review. Med Oral Patol Oral Cir Bucal. 2016 May 1;21(3):e355-66. doi: 10.4317/medoral.20969.
Results Reference
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PubMed Identifier
31261876
Citation
Lysik D, Niemirowicz-Laskowska K, Bucki R, Tokajuk G, Mystkowska J. Artificial Saliva: Challenges and Future Perspectives for the Treatment of Xerostomia. Int J Mol Sci. 2019 Jun 29;20(13):3199. doi: 10.3390/ijms20133199.
Results Reference
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Clinical Study New Gel for Xerostomia

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