UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038320
Receipt number R000043523
Scientific Title Wiping of eyelids after cataract surgery
Date of disclosure of the study information 2019/10/17
Last modified on 2023/02/15 09:37:58

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Basic information

Public title

Wiping of eyelids after cataract surgery

Acronym

Wiping of eyelids after cataract surgery

Scientific Title

Wiping of eyelids after cataract surgery

Scientific Title:Acronym

Wiping of eyelids after cataract surgery

Region

Japan


Condition

Condition

cataract

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effect of wiping of eyelids on Meibomian gland dysfunction after cataract surgery

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

observation of lid
pressing out test

Key secondary outcomes

visual acuity, functional visual acuity, higher order aberrations, Meibography, Break up time, corneal and conjunctival staining, postoperative satisfaction,
Standard Patient Evaluation of Eye Dryness:SPEED


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

subjects group: To wipe eyelids regularly about 1 week to 4 weeks after cataract surgery.

Interventions/Control_2

control group

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

60 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

patients who undergo cataract surgery

Key exclusion criteria

intraoperative complication
wound closure using sutures.

Target sample size

180


Research contact person

Name of lead principal investigator

1st name Kazuno
Middle name
Last name Negishi

Organization

Keio University School of Medicine

Division name

Department of Ophthalmology

Zip code

160-8582

Address

35, Shinanomachi, Shinjuku-ku, Tokyo, Japan

TEL

03-5363-3821

Email

kazunonegishi@keio.jp


Public contact

Name of contact person

1st name Kazuno
Middle name
Last name Negishi

Organization

Keio University School of Medicine

Division name

Department of Ophthalmology

Zip code

160-8582

Address

35, Shinanomachi, Shinjuku-ku, Tokyo, Japan

TEL

03-5363-3821

Homepage URL


Email

kazunonegishi@keio.jp


Sponsor or person

Institute

Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Keio University School of Medicine

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

Keio University School of Medicine

Address

35, Shinanomachi, Shinjuku-ku, Tokyo, Japan

Tel

03-5363-3503

Email

med-rinri-jimu@adst.keio.ac.jp


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

慶應義塾大学病院(東京都)、おおたけ眼科つきみ野医院(神奈川県)


Other administrative information

Date of disclosure of the study information

2019 Year 10 Month 17 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

50

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

2019 Year 10 Month 02 Day

Date of IRB

2019 Year 10 Month 17 Day

Anticipated trial start date

2019 Year 11 Month 01 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2019 Year 10 Month 17 Day

Last modified on

2023 Year 02 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043523


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name