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Efficacy of oil pulling on drug-induced xerostomia

Not Applicable
Conditions
R68.2
Dry mouth, unspecified
Registration Number
DRKS00012459
Lead Sponsor
niklinik KölnAbteilung für Zahnerhaltung und Parodontologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
26
Inclusion Criteria

Minimum age of 18 years

Daily use of at least one drug which has drug-induced xerostomia declared as a side effect in its package insert

xerostomia with minimum level on VAS Skala of 4 to 10

minimum number of four teeth

Exclusion Criteria

allergies relating to the ingredients of the products used in the study (oil)

existing or planned pregnancy during the study

current or anamnestic radiation therapy or chemotherapy

treatment with antibiotics prior to the study

current or anamnestic parotid gland tumor

current or anamnestic tumor in regions of the head or neck

current or anamnestic operation of the head or the neck

Sjögren syndrome

other medical causes for xerostomia which are not drug-induced

current daily use of products which palliate the symptoms of xerostomia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
VAS xerostomic burden investigated by a validated questionnaire at day 0, after use of the first product (day 7), after the washout Phase (day 14) and after use of the second product (day 21).
Secondary Outcome Measures
NameTimeMethod
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