UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000061092
Receipt number R000069906
Scientific Title Impact of Heparin Calcium Supply Discontinuation on Deep Vein Thrombosis Incidence: an observational study
Date of disclosure of the study information 2026/03/28
Last modified on 2026/03/28 10:16:52

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Basic information

Public title

Impact of Heparin Calcium Supply Discontinuation on Deep Vein Thrombosis Incidence: an observational study

Acronym

Impact of Heparin Calcium Supply Discontinuation on Deep Vein Thrombosis Incidence

Scientific Title

Impact of Heparin Calcium Supply Discontinuation on Deep Vein Thrombosis Incidence: an observational study

Scientific Title:Acronym

Impact of Heparin Calcium Supply Discontinuation on Deep Vein Thrombosis Incidence

Region

Japan


Condition

Condition

Deep Vein Thrombosis

Classification by specialty

Medicine in general

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We aimed to verify whether the discontinuation of heparin Ca supply led to an increase in deep vein thrombosis.

Basic objectives2

Others

Basic objectives -Others

epidemiology

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Incidence proportion of DVT events

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients of medical institutions belonging to the Japan Collaborative Network

Key exclusion criteria

Patients without an ICD-10-CM code

Target sample size

4338625


Research contact person

Name of lead principal investigator

1st name Naoto
Middle name M
Last name Ishimaru

Organization

Akashi Medical Center, Japan

Division name

Department of General Internal Medicine

Zip code

6740063

Address

Yagi 743-33 Okubo-cho Akashi, Hyogo

TEL

0789361101

Email

maru-tkb@umin.ac.jp


Public contact

Name of contact person

1st name NAOTO
Middle name
Last name ISHIMARU

Organization

Akashi Medical Center, Japan

Division name

Department of General Internal Medicine

Zip code

6740063

Address

Yagi 743-33 Okubo-cho Akashi, Hyogo

TEL

0789354303

Homepage URL


Email

maru-tkb@umin.ac.jp


Sponsor or person

Institute

Akashi Medical Center

Institute

Department

Personal name



Funding Source

Organization

None

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

Akashi Medical Center

Address

Yagi 743-33 Okubo-cho Akashi, Hyogo

Tel

0789361101

Email

maru-tkb@umin.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

Please Select


Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2026 Year 03 Month 28 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

Enrolling by invitation

Date of protocol fixation

2026 Year 03 Month 09 Day

Date of IRB

2026 Year 03 Month 17 Day

Anticipated trial start date

2026 Year 03 Month 28 Day

Last follow-up date

2026 Year 03 Month 28 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

We compared the incidence proportion of DVT events as a primary outcome by following time flame: Pre-from 24 Aug 2019 to 23 August 2021, out of supply-from 24 August 2021 to 9 July 2023, Post-from 10 July 2023 to 9 July 2025.


Management information

Registered date

2026 Year 03 Month 28 Day

Last modified on

2026 Year 03 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000069906