UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047372
Receipt number R000054032
Scientific Title Comprehensive rapid PCR diagnosis for refractory ocular viral infections
Date of disclosure of the study information 2022/04/06
Last modified on 2023/04/04 16:21:28

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Basic information

Public title

Comprehensive rapid PCR diagnosis for refractory ocular viral infections

Acronym

Comprehensive rapid PCR diagnosis for refractory ocular viral infections

Scientific Title

Comprehensive rapid PCR diagnosis for refractory ocular viral infections

Scientific Title:Acronym

Comprehensive rapid PCR diagnosis for refractory ocular viral infections

Region

Japan


Condition

Condition

ocular viral infections

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To diagnose ocular viral infections with a comprehensive PCR method

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Identification of pathogens from collected ocular fulid samples

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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

Examination of patient's intraocular fulid by real-time PCR.

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients suspected of having ocular viral infections with written consent.

Key exclusion criteria

Patients who do not give consent

Target sample size

400


Research contact person

Name of lead principal investigator

1st name Takehiro
Middle name
Last name Hariya

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

980-8574

Address

1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan

TEL

81-22-717-7294

Email

hari0208pota@oph.med.tohoku.ac.jp


Public contact

Name of contact person

1st name Takehiro
Middle name
Last name Hariya

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Ophthalmology

Zip code

980-8574

Address

1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan

TEL

81-22-717-7294

Homepage URL


Email

hari0208pota@oph.med.tohoku.ac.jp


Sponsor or person

Institute

Department of Ophthalmology, Tohoku University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Ophthalmology, Tohoku University Graduate 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

Tohoku University Graduate School of Medicine Ethics Committee

Address

1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan

Tel

022-717-3867

Email

med-kenkyo@grp.tohoku.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



Other administrative information

Date of disclosure of the study information

2022 Year 04 Month 06 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

Open public recruiting

Date of protocol fixation

2022 Year 04 Month 30 Day

Date of IRB

2022 Year 04 Month 26 Day

Anticipated trial start date

2022 Year 05 Month 01 Day

Last follow-up date

2027 Year 04 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 04 Month 02 Day

Last modified on

2023 Year 04 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000054032


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name