UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057395
Receipt number R000065580
Scientific Title Questionnaire survey on use of antihistamine eye drops and eyelid cream for patients with seasonal allergic conjunctivitis in 2025
Date of disclosure of the study information 2025/03/25
Last modified on 2026/02/17 17:05:44

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Basic information

Public title

Questionnaire survey on use of antihistamine eye drops and eyelid cream for patients with seasonal allergic conjunctivitis in 2025

Acronym

Questionnaire survey on use of antihistamine eye drops and eyelid cream for patients with seasonal allergic conjunctivitis in 2025

Scientific Title

Questionnaire survey on use of antihistamine eye drops and eyelid cream for patients with seasonal allergic conjunctivitis in 2025

Scientific Title:Acronym

Questionnaire survey on use of antihistamine eye drops and eyelid cream for patients with seasonal allergic conjunctivitis in 2025

Region

Japan


Condition

Condition

seasonal allergic conjunctivitis

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate adherence to dosage and usage, the situation of eye itch and treatment satisfaction and reasons for it in patients diagnosed with seasonal allergic conjunctivitis by an ophthalmologist and prescribed antihistamine eye drops and eyelid cream.

Basic objectives2

Others

Basic objectives -Others

To investigate adherence to dosage and usage, the situation of eye itch and treatment satisfaction and reasons for it

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Adherence to dosage and usage
The situation of eye itch
Treatment satisfaction and reasons for it

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Subjects diagnosed with seasonal allergic conjunctivitis by an ophthalmologist and prescribed antihistamine eye drops and eyelid cream after December 2024.
Subjects with seasonal allergic conjunctivitis such as eye itch after December 2024.

Key exclusion criteria

Medical professionals (doctors, pharmacists, nurses, etc.)
Subjects engaged in pharmaceuticals and medical devices industry
Subjects engaged in pharmaceuticals distributor
Subjects engaged in information provision services, research services, and advertising
Subjects with severe allergic conjunctival disease (vernal keratoconjunctivitis , atopic keratoconjunctivitis)

Target sample size

1300


Research contact person

Name of lead principal investigator

1st name Reiko
Middle name
Last name Miyahara

Organization

Santen Pharmaceutical Co., Ltd.

Division name

Japan Medical Affairs Group

Zip code

530-8552

Address

4-20, Ofukacho, Kita-ku, Osaka

TEL

06-4802-9337

Email

clinical@santen.co.jp


Public contact

Name of contact person

1st name Hirotsugu
Middle name
Last name Kishimoto

Organization

Santen Pharmaceutical Co., Ltd.

Division name

Japan Medical Affairs Group

Zip code

530-8552

Address

4-20, Ofukacho, Kita-ku, Osaka

TEL

06-4802-9337

Homepage URL


Email

clinical@santen.co.jp


Sponsor or person

Institute

Santen Pharmaceutical Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Santen Pharmaceutical Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Medical Corporation TOUKEIKAI Kitamachi Clinic ERB

Address

1-1-3,Kichijoji-kitamachi,Musashino-shi,Tokyo,180-0001,Japan

Tel

03-6779-8116

Email

chi-pr-ec-kitamachi@cmicgroup.com


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

2025 Year 03 Month 25 Day


Related information

URL releasing protocol

not applicable

Publication of results

Published


Result

URL related to results and publications

not applicable

Number of participants that the trial has enrolled

799

Results

Adherence to dosage and usage
The proportion of patients who used the medication according to the package insert, regardless of symptom severity, was 22.7% in the EP cream group (n=136), 23.6% in the twice-daily group (n=246), and 3.6% in the four-times-daily group (n=417).

Treatment satisfaction
For treatment satisfaction, "very satisfied" and "satisfied" were 15.4% and 74.3% in the EP cream group, 7.3% and 68.7% in the twice-daily group, and 4.8% and 68.3% in the four-times-daily group.

Results date posted

2026 Year 02 Month 17 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results

2025 Year 11 Month 28 Day

Baseline Characteristics

Refer to published paper

Participant flow

Refer to published paper

Adverse events

Refer to published paper

Outcome measures

Refer to published paper

Plan to share IPD

The datasets are not publicly available, but are available from the corresponding author on reasonable request.

IPD sharing Plan description

The datasets are not publicly available, but are available from the corresponding author on reasonable request.


Progress

Recruitment status

Completed

Date of protocol fixation

2025 Year 03 Month 05 Day

Date of IRB

2025 Year 03 Month 19 Day

Anticipated trial start date

2025 Year 03 Month 24 Day

Last follow-up date

2025 Year 04 Month 03 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Web-based survey of patients diagnosed with seasonal allergic conjunctivitis at an ophthalmologist


Management information

Registered date

2025 Year 03 Month 25 Day

Last modified on

2026 Year 02 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065580