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Malic Acid in Treatment of Xerostomia

Primary Purpose

Xerostomia

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
malic acid
Sponsored by
Hams Hamed Abdelrahman
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Xerostomia

Eligibility Criteria

35 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with type 2 diabetes mellitus suffering from xerostomia.
  • Patients aged between 35 and 50 years old.
  • Glycated hemoglobin less than 7% (28) .
  • Duration of diabetes mellitus not less than 4 years and not more than 8 years.

Exclusion Criteria:

  • Patients receiving any drugs that cause hyposalivation like anti-hypertensive drugs.
  • Patients with any systemic disease reported to produce hyposalivation (sjogren's syndrome, hepatitis c, rheumatoid arthritis and lupus erythematosus) (8).
  • Patients receiving chemo-therapy and radio-therapy.
  • Mouth breathers.

Sites / Locations

  • Faculty of Dentistry, Alexandria UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

malic acid group

placebo group

Arm Description

patients will receive a topical spray containing 1% malic acid

patients will receive a topical placebo spray

Outcomes

Primary Outcome Measures

The unstimulated salivary flow rate
The unstimulated salivary flow rate will be obtained by the spit method every 30s for 15 minutes. Saliva will be collected in graduated tubes. Measurements will be expressed as milliliter per minute. Participants will be asked to refrain from eating, drinking and brushing their teeth at least 2 hours before saliva collection - Hypo-salivation if the unstimulated salivary flow rate 0.1- 0.2 ml/min or less

Secondary Outcome Measures

scoring of severity of xerostomia
Each individual's responses will be scored and summed to give a single score and the higher scores represent more severe symptoms using Xerostomia Inventory-Dutch version

Full Information

First Posted
February 12, 2021
Last Updated
February 12, 2021
Sponsor
Hams Hamed Abdelrahman
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1. Study Identification

Unique Protocol Identification Number
NCT04756986
Brief Title
Malic Acid in Treatment of Xerostomia
Official Title
Efficacy of Malic Acid Spray in Treatment of Xerostomia in Type II Diabetic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
September 1, 2021 (Anticipated)
Study Completion Date
November 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Hams Hamed Abdelrahman

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.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: xerostomia is a subjective sensation of dry mouth resulting from quantitative and /or qualitative changes of saliva. Patients receiving drugs like antihypertensives and antidepressants or patients receiving chemotherapy or radiotherapy for treatment of head and neck cancers may suffer from xerostomia. It also can be experienced in patients with systemic diseases like diabetes mellitus, systemic lupus erythematosus, sjogren's syndrome and rheumatoid arthritis. Malic acid spray with concentration of 1% has grabbed the attention over the last few years as an effective treatment for xerostomia. Study objective: To evaluate the effect of 1% malic acid spray in treatment of xerostomia in type 2 diabetic patients.
Detailed Description
This randomized controlled clinical trial included 52 patients with type 2 diabetes mellitus suffering from xerostomia, divided equally into two groups. Group-I was managed by topical spray containing 1% malic. Group- II was managed by a placebo spray. Both groups received the treatment for 2 weeks. Dry mouth questionnaire scores (DMQ) and unstimulated salivary flow rate was collected before and after treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Xerostomia

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
malic acid group
Arm Type
Experimental
Arm Description
patients will receive a topical spray containing 1% malic acid
Arm Title
placebo group
Arm Type
No Intervention
Arm Description
patients will receive a topical placebo spray
Intervention Type
Drug
Intervention Name(s)
malic acid
Other Intervention Name(s)
hydroxybutanoic
Intervention Description
1% malic acid spray
Primary Outcome Measure Information:
Title
The unstimulated salivary flow rate
Description
The unstimulated salivary flow rate will be obtained by the spit method every 30s for 15 minutes. Saliva will be collected in graduated tubes. Measurements will be expressed as milliliter per minute. Participants will be asked to refrain from eating, drinking and brushing their teeth at least 2 hours before saliva collection - Hypo-salivation if the unstimulated salivary flow rate 0.1- 0.2 ml/min or less
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
scoring of severity of xerostomia
Description
Each individual's responses will be scored and summed to give a single score and the higher scores represent more severe symptoms using Xerostomia Inventory-Dutch version
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with type 2 diabetes mellitus suffering from xerostomia. Patients aged between 35 and 50 years old. Glycated hemoglobin less than 7% (28) . Duration of diabetes mellitus not less than 4 years and not more than 8 years. Exclusion Criteria: Patients receiving any drugs that cause hyposalivation like anti-hypertensive drugs. Patients with any systemic disease reported to produce hyposalivation (sjogren's syndrome, hepatitis c, rheumatoid arthritis and lupus erythematosus) (8). Patients receiving chemo-therapy and radio-therapy. Mouth breathers.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eglal M Mousa, PHD
Organizational Affiliation
Alexandria University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Yasmin Y Gaweesh., PHD
Organizational Affiliation
Alexandria University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Noha K. Abo Aasy, PHD
Organizational Affiliation
Alexandria University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shaimaa A. Muhamed, BDS
Organizational Affiliation
Alexandria University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Dentistry, Alexandria University
City
Alexandria
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shaimaa A Muhamed, BDS
Phone
00201023314177
Email
shaymaa.abdelnabi@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The investigators are planning to share the methods and the results of this study with all the investigators
IPD Sharing Time Frame
starting 6 months after publication
IPD Sharing Access Criteria
he sharing access can be through PubMed when the study is published or through direct contact through this email

Learn more about this trial

Malic Acid in Treatment of Xerostomia

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