Study Results
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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COMPLETED
NA
60 participants
INTERVENTIONAL
2011-08-31
2012-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
TRIPLE
Study Groups
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0.1% pilocarpine mouthwash
0.1% pilocarpine solution which diluted 2% pilocarpine hydrochloride eyedrop with 0.9% saline
Pilocarpine
0.1% pilocarpine solution which diluted 2% pilocarpine hydrochloride eyedrop with 0.9% saline.
subjects were instructed to mouthwash with 10ml of solution for 1 minute.
0.9% saline mouthwash
0.9% saline as a mouthwash
saline
0.9% saline solution
Interventions
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Pilocarpine
0.1% pilocarpine solution which diluted 2% pilocarpine hydrochloride eyedrop with 0.9% saline.
subjects were instructed to mouthwash with 10ml of solution for 1 minute.
saline
0.9% saline solution
Eligibility Criteria
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Inclusion Criteria
* adults aged 20 years and older.
Exclusion Criteria
* acute iritis
* narrow angle glaucoma
* pilocarpine allergy
* pregnancy
* lactating women, and
* person who was treating xerostomia with artificial saliva, pilocarpine, or etc.
20 Years
ALL
No
Sponsors
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Jeong-seong Kwon
OTHER
Responsible Party
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Jeong-seong Kwon
Clinical assistant professor
Principal Investigators
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Jeong-Seung Kwon, DDS,MSD,PhD
Role: PRINCIPAL_INVESTIGATOR
Yonsei University Dental Hospital
Locations
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Yonsei University Dental Hospital
Seoul, Seoul, South Korea
Countries
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Other Identifiers
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2-2011-0032
Identifier Type: -
Identifier Source: org_study_id
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