Rotation Stability of Toric Intraocularlens (IOL) Compared Sitting Against Lying After Cataract Operation

NCT ID: NCT04776057

Last Updated: 2022-10-13

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

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-01

Study Completion Date

2023-12-30

Brief Summary

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To assess the rotation stability of toric intraocular lenses between sitting or routine settings (sitting, going around) after cataract operation.

Detailed Description

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To assess the rotation stability of toric intraocular lenses between sitting or routine settings (sitting, going around) after cataract operation.

Conditions

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Astigmatism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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lying

after cataract lying for 1 hour

Group Type OTHER

catarct surgery with toric intra ocular lenses

Intervention Type OTHER

rotation stability of toric intraocular lenses between sitting or routine settings (sitting, going around) after cataract operation

sitting, walkin

after cataract sitting or walking for 1 hour

Group Type OTHER

catarct surgery with toric intra ocular lenses

Intervention Type OTHER

rotation stability of toric intraocular lenses between sitting or routine settings (sitting, going around) after cataract operation

Interventions

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catarct surgery with toric intra ocular lenses

rotation stability of toric intraocular lenses between sitting or routine settings (sitting, going around) after cataract operation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Cataract
* Age 21 and older
* Regular corneal astigmatism ≥ 1.5 D
* written informed consent prior to surgery

Exclusion Criteria

* Relevant other ophthalmic diseases such as: pseudoexfoliation, traumatic cataract corneal scars, and other co-morbidity that could affect capsule bag stability ( e.g. Marfan syndrome)
* High myopia (\> 29 mm AL)
* Irregular corneal astigmatism on corneal topography
* In case of pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Prim. Prof. Dr. Oliver Findl, MBA

OTHER

Sponsor Role lead

Responsible Party

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Prim. Prof. Dr. Oliver Findl, MBA

Prof Oliver Findl

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Hanusch Hospital, Department of Ophthalmology

Vienna, , Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Julius Hienert, MD

Role: CONTACT

+436646415113

Facility Contacts

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Oliver Findl, Prof. MD

Role: primary

+43 1 91021 57564

Other Identifiers

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EK 20-302-1220

Identifier Type: -

Identifier Source: org_study_id

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