UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000034777
Receipt number R000039659
Scientific Title Evaluation of rapid diagnostic test for RS virus and adenovirus infection
Date of disclosure of the study information 2020/12/01
Last modified on 2024/01/25 09:07:59

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Basic information

Public title

Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Acronym

Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Scientific Title

Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Scientific Title:Acronym

Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Region

Japan


Condition

Condition

respiratory syncytial virus (RSV) infection, adenovirus infection

Classification by specialty

Infectious disease Pediatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sensitivity, specificity and detection limit of rapid diagnostic test for RS virus and adenovirus infection

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

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Maneuver Other

Interventions/Control_1

Sample collection, assay with test kit

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 that visit the medical institution during this study, and include the following conditions:
1) Patients with suspected RSV or Adeno virus infection based on symptoms.
2) Patients who agree to participate in this study.

Key exclusion criteria

1) Patients who are difficult to obtain clinical samples from.
2) For any reason other than above, patients who were determined by doctor as being unfit to participate in this study.

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Keiko
Middle name
Last name Mitamura

Organization

Eiju General Hospital

Division name

Division for infection control

Zip code

110-8645

Address

2-23-16 Higashi-ueno, Taito-ku Tokyo 110-8645, Japan

TEL

03-3833-8381

Email

mitamurakeiko77@gmail.com


Public contact

Name of contact person

1st name Yuta
Middle name
Last name Maehara

Organization

Sekisui Medical Co., Ltd.

Division name

Research & Development

Zip code

103-0027

Address

1-3 Nihonbashi 2-chome, Chuo-ku Tokyo 103-0027, Japan

TEL

03-3272-0677

Homepage URL


Email

yuta.maehara@sekisui.com


Sponsor or person

Institute

Sekisui Medical Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Sekisui Medical Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

Zama Children's Clinic, Ichikawa Children's Clinic, Abe Children's Clinic, Kobayashi International Clinic, Jichi Medical University

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

座間小児科診療所(神奈川県)、市川こどもクリニック(神奈川県)、あべこどもクリニック(神奈川県)、小林国際クリニック(神奈川県)、自治医科大学(栃木県)、永寿総合病院(東京都)


Other administrative information

Date of disclosure of the study information

2020 Year 12 Month 01 Day


Related information

URL releasing protocol

https://www.info.pmda.go.jp/tgo/pack/30200EZX00014000_A_01_03/

Publication of results

Published


Result

URL related to results and publications

https://www.info.pmda.go.jp/tgo/pack/30200EZX00014000_A_01_03/

Number of participants that the trial has enrolled

873

Results

1) Control method: PCR
Positive predictive value (sensitivity)
RSV: 96.1 ~ 98.1%
Adeno: 93.1 ~ 96.6%
Negative concordance (specificity)
RSV: 100%
Adeno: 100%

2) Control method: Approved products
Positive predictive value (sensitivity)
RSV: 99.6%
Adeno: 92.9 ~ 97.1%
Negative concordance (specificity)
RSV: 97.8%
Adeno: 99.3 ~ 99.8%

Results date posted

2021 Year 12 Month 15 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

NA

Participant flow

Specimens were collected from patients who obtained consent using the informed consent form and used for testing.

Adverse events

NA

Outcome measures

positive concordance rate
negative concordance rate

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2018 Year 10 Month 15 Day

Date of IRB

2018 Year 10 Month 09 Day

Anticipated trial start date

2018 Year 11 Month 01 Day

Last follow-up date

2019 Year 08 Month 31 Day

Date of closure to data entry

2019 Year 09 Month 15 Day

Date trial data considered complete

2019 Year 09 Month 30 Day

Date analysis concluded

2019 Year 10 Month 04 Day


Other

Other related information



Management information

Registered date

2018 Year 11 Month 05 Day

Last modified on

2024 Year 01 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039659


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name