UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000007820
Receipt number R000001265
Scientific Title A Randamized, Prospective and Comparative Study of Topical Timolol and Latanoprost in Uveitic Glaucoma
Date of disclosure of the study information 2012/04/23
Last modified on 2018/04/28 16:19:26

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Basic information

Public title

A Randamized, Prospective and Comparative Study of Topical Timolol and Latanoprost in Uveitic Glaucoma

Acronym

A Comparative Study of Topical Timolol and Latanoprost in Uveitic Glaucoma

Scientific Title

A Randamized, Prospective and Comparative Study of Topical Timolol and Latanoprost in Uveitic Glaucoma

Scientific Title:Acronym

A Comparative Study of Topical Timolol and Latanoprost in Uveitic Glaucoma

Region

Japan


Condition

Condition

Uveitic Glaucoma

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We evaluated effects on the intraocular pressure (IOP) lowering and safety of topical timolol and latanoprost in UG prospectively.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

intraocular pressure-lowering ratio

Key secondary outcomes

1)flare value in the anterior chamber
2)side effects(conjunctival injection, corneal erosion)
3)macular thickness measured by OCT


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

NO

Dynamic allocation

YES

Institution consideration

Institution is considered as a block.

Blocking

YES

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Latanoprost eye drop

Interventions/Control_2

Timolol-XE eye drop

Interventions/Control_3


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1)The patients received topical corticosteroid for uveitis.
2) There was no strong inflammation in the anterior chamber within these 3 months.
3) The objective eyes didn't received anti-glaucoma eye drops.
4) 30mmHg> Baseline IOP (before starting treatment) >=21mmHg

Key exclusion criteria

1) herpetic iritis
2) PAS index>25% (secondary angle closure glaucoma)
3) The patients who received Argon Laser Trabeculoplasty within 3 months.
4) The patients who received intraocular surgeries within 6 months.
5)The patients who had asthma or arrythmia, and couldn't receive timolol.

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshikatsu Kaburaki

Organization

University of Tokyo Hospital

Division name

Ophthalmology

Zip code


Address

7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan

TEL

03-3815-5411

Email

kabutosi-tky@umin.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Toshikatsu Kaburaki

Organization

University of Tokyo Hospital

Division name

Ophthalmology

Zip code


Address

7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan

TEL

03-3815-5411

Homepage URL


Email

kabutosi-tky@umin.ac.jp


Sponsor or person

Institute

Deportment of Ophthalmology, University of Tokyo Hospital

Institute

Department

Personal name



Funding Source

Organization

Deportment of Ophthalmology, University of Tokyo Hospital

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Department of Ophthalmology, Teikyo University Hospital

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

東京大学附属病院眼科(東京都)


Other administrative information

Date of disclosure of the study information

2012 Year 04 Month 23 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

Completed

Date of protocol fixation

2007 Year 02 Month 01 Day

Date of IRB


Anticipated trial start date

2008 Year 02 Month 01 Day

Last follow-up date

2015 Year 12 Month 01 Day

Date of closure to data entry

2016 Year 03 Month 01 Day

Date trial data considered complete

2016 Year 06 Month 01 Day

Date analysis concluded

2017 Year 12 Month 01 Day


Other

Other related information



Management information

Registered date

2012 Year 04 Month 23 Day

Last modified on

2018 Year 04 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001265


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name