UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006852
Receipt number R000008100
Scientific Title Comparison between toric and non-toric intraocular lens implantation in patients approved for toric intraocular lens implantation.
Date of disclosure of the study information 2011/12/07
Last modified on 2011/12/07 14:07:04

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Basic information

Public title

Comparison between toric and non-toric intraocular lens implantation in patients approved for toric intraocular lens implantation.

Acronym

The clinical result of toric intraocular lens

Scientific Title

Comparison between toric and non-toric intraocular lens implantation in patients approved for toric intraocular lens implantation.

Scientific Title:Acronym

The clinical result of toric intraocular lens

Region

Japan


Condition

Condition

Cataract

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare toric and non-toric intraolucar lens implantation in patients both approved and not approved for toric IOL implantation

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Postoperative data of uncorrected visual acuity

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

toric intraocular lens implantation in patients eligible for toric lens

Interventions/Control_2

non-toric intraocular lens implatation in patients ineligible for toric lens

Interventions/Control_3

non-toric intraocular lens implatation in patients eligible for toric lens

Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Catract patients undergoing implantation with AcrySoF toric intraocular lens

Key exclusion criteria

Patients found to have other ocular diseases or a postoperative spherical error target other than emmetropia were excluded from the study.

Target sample size

500


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hitoshi Tabuchi

Organization

Saneikai Tsukazaki Hospital

Division name

Department of Ophthalmology

Zip code


Address

68-1 Waku Aboshi-ku Himeji HYOGO,JAPAN

TEL

0792728555

Email



Public contact

Name of contact person

1st name
Middle name
Last name Hitoshi Tabuchi

Organization

Saneikai Tsukazaki Hospital

Division name

Department of Ophthalmology

Zip code


Address

68-1 Waku Aboshi-ku Himeji HYOGO,JAPAN

TEL

0792728555

Homepage URL


Email

H.Tabuchi@tuskazaki-eye.net


Sponsor or person

Institute

Saneikai Tsukazaki Hospital

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

ツカザキ病院(兵庫県)


Other administrative information

Date of disclosure of the study information

2011 Year 12 Month 07 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2009 Year 07 Month 31 Day

Date of IRB


Anticipated trial start date

2009 Year 09 Month 01 Day

Last follow-up date

2011 Year 11 Month 01 Day

Date of closure to data entry

2011 Year 12 Month 01 Day

Date trial data considered complete

2011 Year 12 Month 01 Day

Date analysis concluded

2011 Year 12 Month 01 Day


Other

Other related information



Management information

Registered date

2011 Year 12 Month 07 Day

Last modified on

2011 Year 12 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008100


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name