Alternative Application Methods of Pre-procedural Povidone Iodine Mouthrinse

NCT ID: NCT06272019

Last Updated: 2024-04-23

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

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-01

Study Completion Date

2024-04-20

Brief Summary

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To compare the iodine remaining in saliva between gargle method and swab method

Detailed Description

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separate the participant in 2 groups group 1 use iodine gargle with gargle method, after 48 hours use iodine gargle with swab method group 2 use iodine gargle with swab method, after 48 hours use iodine gargle with gargle method The researcher will collect saliva before use iodine gargle and after use at time 0, 5, 10, 20, 30, 60, 120 minutes

Conditions

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The Retention of Iodine in Saliva Over the Time The Comparison of Iodine in Saliva Between Gargle and Swab

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

the participant will use iodine gargle in 2 method
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Gargle method

the participant will use 0.2% iodine gargle with gargle method by hold in mouth 30 second and gargle 30 seconds after that spit out

Group Type EXPERIMENTAL

Iodine gargle

Intervention Type OTHER

Iodine gargle 0.2 %

Swab method

the participant will use 0.2 iodine gargle with swab method by the researcher apply on mouth 1 minute without spit out

Group Type EXPERIMENTAL

Iodine gargle

Intervention Type OTHER

Iodine gargle 0.2 %

Interventions

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Iodine gargle

Iodine gargle 0.2 %

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Thai people
* no underlying disease, no pregnant
* at least 24 teeth
* No use iodine gargle
* No allergy to iodine and seafood
* No orthodontic and prosthetic treatment
* No ulcer and edentulous area
* Saliva flow rate in male (0.57+-0.3 ml/minute), in woman (0.41+-0.27 ml/minute)
* PI score lower than 0.6 (Green and vermillion index)

Exclusion Criteria

* treatment orthodontic or prosthetic treatment currently
* Allergy to iodine between reach
* Can not participate
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Chulalongkorn University

OTHER

Sponsor Role lead

Responsible Party

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Wannakorn Sriarj

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Wannakorn Sriar

Role: PRINCIPAL_INVESTIGATOR

Faculty of Dentistry, Chulalongkorn University

Locations

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Faculty of Dentistry, Chulalongkorn University

Bangkok, , Thailand

Site Status

Countries

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Thailand

References

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Related Links

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Other Identifiers

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HREC-DCU 2023-074

Identifier Type: -

Identifier Source: org_study_id

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