UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009438
Receipt number R000011079
Scientific Title Effect of Diquafosol Sodium Eye Drops on Tear Film Stability
Date of disclosure of the study information 2012/12/01
Last modified on 2012/11/29 21:07:32

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Basic information

Public title

Effect of Diquafosol Sodium Eye Drops on Tear Film Stability

Acronym

Effect of Diquafosol Sodium Eye Drops on Tear Film Stability

Scientific Title

Effect of Diquafosol Sodium Eye Drops on Tear Film Stability

Scientific Title:Acronym

Effect of Diquafosol Sodium Eye Drops on Tear Film Stability

Region

Japan


Condition

Condition

unstable tear film type of dry eye disease

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effect of diquafosol sodium eye drops on tear film stability in patients with unstable tear film.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

tear film break-up time, tear secretion, ocular surface damage, tear film stability, subjective symptom

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

diquafosol sodium eye drop

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

99 years-old >=

Gender

Male and Female

Key inclusion criteria

1) presence of DED symptoms
2) Schirmers value more than 5 mm
3) BUT equal or less than 5 seconds
4) fluorescein score equal or less than 3 points (9 points maximum).

Key exclusion criteria

Eyes with contact lens wearing, active ocular surface disorders other than DED, history of ocular surgeries, presence of punctual plugs, meibomian gland dysfunction with more than moderate degree of severity, and receiving eye drops other than artificial tears or hyaluronic acid were excluded.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Seika Shimazaki-Den

Organization

Tokyo Dental College

Division name

Opthalmology

Zip code


Address

5-11-13, Sugano, Ichikawa, Chiba, Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Tokyo Dental College Ichikawa General Hospital

Division name

Institutional Review Board

Zip code


Address


TEL

047-322-0151

Homepage URL


Email



Sponsor or person

Institute

Tokyo Dental College Ichikawa General Hospital

Institute

Department

Personal name



Funding Source

Organization

Tokyo Dental College Ichikawa General Hospital

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

2012 Year 12 Month 01 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

2011 Year 01 Month 18 Day

Date of IRB


Anticipated trial start date

2011 Year 06 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2012 Year 11 Month 29 Day

Last modified on

2012 Year 11 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011079


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name