Short Term Refractive and Ocular Parameter Changes After Topical Atropine
NCT ID: NCT03839888
Last Updated: 2019-02-15
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
96 participants
INTERVENTIONAL
2015-01-01
2015-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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0.125% atropine group
patients used the 0.125 % atropine eyedrop every night before sleep for 7 days
0.125% Atropine
patients used 0.125% atropine eyedrop per night before sleep for 7 days.
Interventions
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0.125% Atropine
patients used 0.125% atropine eyedrop per night before sleep for 7 days.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
3 Years
18 Years
ALL
No
Sponsors
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Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
OTHER
Responsible Party
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References
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Ho MC, Hsieh YT, Shen EP, Hsu WC, Cheng HC. Short-term refractive and ocular parameter changes after topical atropine. Taiwan J Ophthalmol. 2019 Feb 20;10(2):111-115. doi: 10.4103/tjo.tjo_110_18. eCollection 2020 Apr-Jun.
Other Identifiers
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BuddhistTCGHTaipei2
Identifier Type: -
Identifier Source: org_study_id
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