Lipid Based Food Additives for Treating Patients With Dry Mouth

NCT ID: NCT00422370

Last Updated: 2007-01-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-01-31

Brief Summary

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Over 10% of adult population suffers from dry mouth (xerostomia). The aim of this double blind prospective clinical trial is to examine a new lipid based food additive formulation to ease mouth dryness in these patients.

Detailed Description

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Conditions

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Xerostomia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

DOUBLE

Interventions

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lipid based additives based on vegetable oil & lecithin

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Dry mouth patients

Exclusion Criteria

* Disabled patients
* Pregnant
* Full upper denture
* Under 18 years old
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hadassah Medical Organization

OTHER

Sponsor Role lead

Principal Investigators

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Doron J Aframian, DMD PhD

Role: STUDY_CHAIR

Reference: Kelly HM et al. Bioadhesive,rheological, lubricant and other aspectes of an oral gel formulation intended for the treatment of xerostomia. Int J Phramac. 2004; 278: 391-406

Doron J Aframian, DMD PhD

Role: STUDY_CHAIR

Salivary Gland Clinic, Department of Oral Medicine The Hebrew University-Hadassah School of Dental Medicine Jerusalem, Israel P.O.B 12272, Zip code 91120

Central Contacts

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Doron J Aframian, DMD PhD

Role: CONTACT

0097226776151

Other Identifiers

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38-29.12.06

Identifier Type: -

Identifier Source: org_study_id

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