UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051273
Receipt number R000058480
Scientific Title Evaluation of a diagnostic COVID-19 infection based on fecal analysis and consideration of the risks in endoscopic procedures
Date of disclosure of the study information 2023/06/06
Last modified on 2023/12/13 15:59:10

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Basic information

Public title

Fecal PCR test with COVID-19 during endoscopic procedures

Acronym

COVID-19 fecal PCR test

Scientific Title

Evaluation of a diagnostic COVID-19 infection based on fecal analysis and consideration of the risks in endoscopic procedures

Scientific Title:Acronym

Effect of COVID-19 infection on the gastrointestinal tract considering preventive methods during endoscopic procedures

Region

Japan


Condition

Condition

patients with diagnosed COVID-19

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study aimed to evaluate the risk of infection in patients with coronavirus disease 2019 (COVID-19) in relation to the gastrointestinal tract using fecal polymerase chain reaction (PCR) tests.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The detection of SARS-Cov-2 in human stool samples in nasal mucosa PCR-positive individuals

Key secondary outcomes



Base

Study type

Observational


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients diagnosed COVID-19 with nasal PCR-positive at Tokyo Medical University Hospital, and obtained informed consent

Key exclusion criteria

Patients who could not give consent to participate in this study.
Those who have serious complications (heart failure, renal failure, liver failure, respiratory failure)
Other patients who are deemed inappropriate to participate in this study.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Sakiko
Middle name
Last name Naito

Organization

Tokyo Medical University

Division name

Department of Gastroenterology and Hepatology

Zip code

160-0023

Address

6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo, Japan

TEL

0333426111

Email

sakiko-n@tokyo-med.ac.jp


Public contact

Name of contact person

1st name Sakiko
Middle name
Last name Naito

Organization

Tokyo Medical University

Division name

Department of Gastroenterology and Hepatology

Zip code

160-0023

Address

6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo, Japan

TEL

0333426111

Homepage URL


Email

sakiko-n@tokyo-med.ac.jp


Sponsor or person

Institute

Tokyo Medical University

Institute

Department

Personal name



Funding Source

Organization

Tokyo Medical University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tokyo Medical University

Address

6-7-1,Nishishinjuku, Shinjuku-ku, Tokyo, Japan

Tel

0333426111

Email

sakiko-n@tokyo-med.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

2023 Year 06 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

2021 Year 05 Month 07 Day

Date of IRB

2021 Year 10 Month 26 Day

Anticipated trial start date

2022 Year 01 Month 01 Day

Last follow-up date

2023 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2023 Year 12 Month 31 Day


Other

Other related information

We are reviewing a case study.


Management information

Registered date

2023 Year 06 Month 06 Day

Last modified on

2023 Year 12 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058480


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name