UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013633
Receipt number R000015912
Scientific Title Effects of mydriatic and miotic pupil on kinetic perimetry
Date of disclosure of the study information 2014/04/04
Last modified on 2015/07/23 10:01:48

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Effects of mydriatic and miotic pupil on kinetic perimetry

Acronym

Effects of mydriatic and miotic pupil on kinetic perimetry

Scientific Title

Effects of mydriatic and miotic pupil on kinetic perimetry

Scientific Title:Acronym

Effects of mydriatic and miotic pupil on kinetic perimetry

Region

Japan


Condition

Condition

Normal Subject

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects of mydriatic and miotic pupil on the kinetic sensitivity with kinetic perimetry in normal eyes.

Basic objectives2

Bio-equivalence

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

kinetic sensitivity measured with automated kinetic perimetry in baseline, mydriatic, and miotic pupil.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Medicine Device,equipment

Interventions/Control_1

baseline pupil
mydriatic pupil
miotic pupil

Interventions/Control_2


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

60 years-old >

Gender

Male and Female

Key inclusion criteria

Corrected VA of 20/20 or better
IOPs of 21 mmHg or less
Normal optic disc
Open angle
No ophthalmic diseases

Key exclusion criteria

Corrected VA of 20/20 or less
IOPs of 21 mmHg or more
Glaucoma like disc
narrow angle
Ophthalmic diseases

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazunori Hirasawa

Organization

Kitasato University

Division name

School of Allied Health Sciences

Zip code


Address

1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0374

TEL

042-778-9671

Email

hirasawa@kitasato-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kazunori Hirasawa

Organization

Kitasato University

Division name

School of Allied Health Sciences

Zip code


Address

1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0374, Japan.

TEL

042-778-9671

Homepage URL


Email

hirasawa@kitasato-u.ac.jp


Sponsor or person

Institute

Kitasato University

Institute

Department

Personal name



Funding Source

Organization

Kitasato University

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



Other administrative information

Date of disclosure of the study information

2014 Year 04 Month 04 Day


Related information

URL releasing protocol


Publication of results

Published


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

2013 Year 01 Month 15 Day

Date of IRB


Anticipated trial start date

2014 Year 04 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2014 Year 10 Month 29 Day


Other

Other related information



Management information

Registered date

2014 Year 04 Month 04 Day

Last modified on

2015 Year 07 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015912


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name