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Early Phase Study Comparing the Effectiveness of a Dairy Product With the Reference Treatment Aequasyal® on Dry Mouth Symptoms in Patients Suffering From Xerostomia Caused by Psychotropic Medications. (LactoXeros)

Primary Purpose

Xerostomia

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Dairy product
Aequasyal mouth spray
Sponsored by
Centre Hospitalier Universitaire de Besancon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Xerostomia focused on measuring xerostomia, Saliva, iatrogenic oral dryness, dairy product

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over 18 years old
  • Patients seen in the psychiatry department requiring the prescription of psychotropic drugs (antidepressants anxiolytics) for over 6 weeks
  • Patients complaining of xerostomia
  • Patients having not taken a palliative therapy against xerostomia for at least 2 weeks
  • Patients having signed a free and informed consent form
  • Patients affiliated to a social security system

Exclusion Criteria:

  • Patients suffering from psychotic illness
  • Patients suffering from Sjogren's syndrome
  • Patients having been treated by radiation therapy for head or neck cancer
  • Patients having stopped a palliative therapy against xerostomia for less than 2 weeks
  • Patients under 18
  • Pregnant or Breastfeeding women
  • Incapacitated adults
  • Patients placed under tutorship or curatorship
  • Patients under judicial protection
  • Patients suffering from milk allergy or lactose intolerance

Sites / Locations

  • CHU de BesanconRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Dairy product

Aequasyal mouth spray medical device

Arm Description

The product will be taken for 14 days

The spray will be taken for 14 days

Outcomes

Primary Outcome Measures

Comparison of changes in mouth Dryness Score
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21

Secondary Outcome Measures

Difficulty in chewing
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Difficulty in swallowing
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Difficulty in speaking
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Burning sensation
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Taste perception
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Silness-Loe Index measuring dental plaque
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Salivary flow
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Saliva pH
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21

Full Information

First Posted
February 3, 2016
Last Updated
October 5, 2017
Sponsor
Centre Hospitalier Universitaire de Besancon
Collaborators
Ecole Nationale de l'Industrie Laitière (ENIL), Centre Hospitalier Universitaire Dijon
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1. Study Identification

Unique Protocol Identification Number
NCT02705937
Brief Title
Early Phase Study Comparing the Effectiveness of a Dairy Product With the Reference Treatment Aequasyal® on Dry Mouth Symptoms in Patients Suffering From Xerostomia Caused by Psychotropic Medications.
Acronym
LactoXeros
Official Title
Early Phase Study Comparing the Effectiveness of a Dairy Product, Co-developed by Besancon University Hospital and the National School of Dairy Industry (ENIL), With the Reference Treatment Aequasyal® on Dry Mouth Symptoms in Patients Suffering From Xerostomia Caused by Psychotropic Medications.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 13, 2017 (Actual)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
March 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Besancon
Collaborators
Ecole Nationale de l'Industrie Laitière (ENIL), Centre Hospitalier Universitaire Dijon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Dry mouth symptoms mostly occur as drug side-effects. Available products such as saliva substitutes are disappointing (bad taste, poor efficiency). The hypothesis stems from the "empirical" observations that many patients alleviate dry mouth symptoms by the consumption of dairy products. Through its composition, the dairy product in itself provides relief for the patient, due both to its physical and biochemical properties, which could explain these observed improvements, and to elements related to the phenomena of consumption of food as an alternative to medication. In the latter case, hedonism takes on a role which has not been previously assessed. Initial work undertaken with the department of applied research at the National Dairy Industry School (ENIL) led to the prototyping of a new milk product, to qualify and adapt a product with a "health benefit" in patients suffering from xerostomia. This dairy product has specific taste, texture and lubrication properties and will be tested in a randomized controlled cross-over study for its efficiency and acceptability versus a reference product (Aequasyal ®, Oxidized Glycerol Triester) on a group of 32 patients at Dijon and at Besançon University Hospitals. This way of combatting xerostomia at the interface of patients' diet, such as it is proposed here, could help improve their quality of life, minimize harmful effects (infection, decay) and promote adherence to treatments which are responsible for xerostomia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Xerostomia
Keywords
xerostomia, Saliva, iatrogenic oral dryness, dairy product

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dairy product
Arm Type
Experimental
Arm Description
The product will be taken for 14 days
Arm Title
Aequasyal mouth spray medical device
Arm Type
Active Comparator
Arm Description
The spray will be taken for 14 days
Intervention Type
Other
Intervention Name(s)
Dairy product
Intervention Description
Dairy products are given to patients with the instruction to eat as many products as necessary to provide them with some relief (within a limit of 6 per day) for 14 days
Intervention Type
Device
Intervention Name(s)
Aequasyal mouth spray
Intervention Description
The mouth spray will be used by patients as needed (according to the package leaflet) for 14 days
Primary Outcome Measure Information:
Title
Comparison of changes in mouth Dryness Score
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Secondary Outcome Measure Information:
Title
Difficulty in chewing
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Title
Difficulty in swallowing
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Title
Difficulty in speaking
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Title
Burning sensation
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Title
Taste perception
Description
Change (in centimeters measured on a Visual Analogue Scale) determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Score measured at day 0, day 14, Day 21 and day 35
Title
Silness-Loe Index measuring dental plaque
Description
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Measured at day 0, day 14, Day 21 and day 35
Title
Salivary flow
Description
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Measured at day 0, day 14, Day 21 and day 35
Title
Saliva pH
Description
Change determined between day 14 and day 0 will be compared to the change assessed between day 35 and day 21
Time Frame
Measured at day 0, day 14, Day 21 and day 35

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over 18 years old Patients seen in the psychiatry department requiring the prescription of psychotropic drugs (antidepressants anxiolytics) for over 6 weeks Patients complaining of xerostomia Patients having not taken a palliative therapy against xerostomia for at least 2 weeks Patients having signed a free and informed consent form Patients affiliated to a social security system Exclusion Criteria: Patients suffering from psychotic illness Patients suffering from Sjogren's syndrome Patients having been treated by radiation therapy for head or neck cancer Patients having stopped a palliative therapy against xerostomia for less than 2 weeks Patients under 18 Pregnant or Breastfeeding women Incapacitated adults Patients placed under tutorship or curatorship Patients under judicial protection Patients suffering from milk allergy or lactose intolerance
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nazim NEKROUF, MD
Phone
0033.3.81.21.82.75
Email
n1nekrouf@chu-besancon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Gaelle Brunotte, PharmD
Email
gbrunotte@chu-besancon.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nazim NEKROUF, MD
Organizational Affiliation
Besancon University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Besancon
City
Besançon
ZIP/Postal Code
25000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nazim NEKROUF, MD

12. IPD Sharing Statement

Learn more about this trial

Early Phase Study Comparing the Effectiveness of a Dairy Product With the Reference Treatment Aequasyal® on Dry Mouth Symptoms in Patients Suffering From Xerostomia Caused by Psychotropic Medications.

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