UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000023637
Receipt number R000027006
Scientific Title Analysis of risk factors of bleeding after endoscopic surgery and evaluation of perioperative safety for users of anticoagulants
Date of disclosure of the study information 2016/08/16
Last modified on 2020/06/18 20:05:44

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Analysis of risk factors of bleeding after endoscopic surgery and evaluation of perioperative safety for users of anticoagulants

Acronym

Management of the anticoagulant in endoscopic surgery

Scientific Title

Analysis of risk factors of bleeding after endoscopic surgery and evaluation of perioperative safety for users of anticoagulants

Scientific Title:Acronym

Management of the anticoagulant in endoscopic surgery

Region

Japan


Condition

Condition

gastric cancer, esophageal cancer, colon polyp, colon cancer

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To analyze risk factors of bleeding after endoscopic surgery and to evaluate validity and safety of perioperative discontinuation of anticoagulants

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Bleeding rates and risk factors for bleeding after endoscopic surgery

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

Users of anticoagulants who receive endoscopic surgery

Key exclusion criteria

Patients who are not adequate to study

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shoko Ono

Organization

Hokkaido University Hospital

Division name

Divison of Endoscopy

Zip code


Address

Kita-14, Nishi-5, Kita-ku, Sapporo, Japan

TEL

0117161161

Email

onosho@med.hokudai.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shoko Ono

Organization

Hokkaido University Hospital

Division name

Divison of Endoscopy

Zip code


Address

Kita-14, Nishi-5, Kita-ku, Sapporo, Japan

TEL

0117161161

Homepage URL


Email

onosho@med.hokudai.ac.jp


Sponsor or person

Institute

Department of Gastroenterology, Hokkaido University Hospital

Institute

Department

Personal name



Funding Source

Organization

Self funding

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


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

北海道大学病院(北海道)


Other administrative information

Date of disclosure of the study information

2016 Year 08 Month 16 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

Completed

Date of protocol fixation

2016 Year 08 Month 09 Day

Date of IRB

2016 Year 08 Month 09 Day

Anticipated trial start date

2016 Year 08 Month 09 Day

Last follow-up date

2019 Year 01 Month 31 Day

Date of closure to data entry

2019 Year 01 Month 31 Day

Date trial data considered complete

2019 Year 03 Month 31 Day

Date analysis concluded

2019 Year 06 Month 30 Day


Other

Other related information

To evaluate bleeding and embolic events after endoscopic surgery for one month.



Management information

Registered date

2016 Year 08 Month 16 Day

Last modified on

2020 Year 06 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027006


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name