UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056702
Receipt number R000064819
Scientific Title Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years
Date of disclosure of the study information 2025/03/01
Last modified on 2026/06/07 05:58:37

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Basic information

Public title

Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years

Acronym

Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years

Scientific Title

Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years

Scientific Title:Acronym

Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years

Region

Japan


Condition

Condition

Ulcerative colitis

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1


The aim of this study is to perform the retrospective observation of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

persistence of golimumab treatment at the induction, one and two year

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 treated with golimumab in our hospital

Key exclusion criteria

1. patients who called us to refuse to join this study
2. patients whose information was not able to extract from their patient's record

Target sample size

130


Research contact person

Name of lead principal investigator

1st name Shingo
Middle name
Last name Kato

Organization

Saitama Medical Center, Saitama Medicla University

Division name

Department of Gastroenterology and Hepatology

Zip code

350-8550

Address

1981, Kamoda, Kawagoe City, Saitama, Japan

TEL

0492283564

Email

skato@saitama-med.ac.jp


Public contact

Name of contact person

1st name Shingo
Middle name
Last name Kato

Organization

Saitama Medical Center, Saitama Medical University

Division name

Department of Gastroenterology and Hepatology

Zip code

350-8550

Address

1981, Kamoda, Kawagoe City, Saitama, Japan

TEL

0492283564

Homepage URL


Email

skato@saitama-med.ac.jp


Sponsor or person

Institute

Saitama Medical Center, Saitama Medical University

Institute

Department

Personal name



Funding Source

Organization

Saitama Medical Center, Saitama 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

IRB in Saitama Medical Center

Address

1981, Kamoda, Kawagoe City, Saitama, Japan

Tel

0492283902

Email

smcrinri@saitama-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

2025 Year 03 Month 01 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

2025 Year 03 Month 01 Day

Date of IRB

2025 Year 03 Month 06 Day

Anticipated trial start date

2025 Year 03 Month 06 Day

Last follow-up date

2027 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Retrospective single center observational study of usefulness and safety of golimumab in patients with inflammatory bowel diseases for two years


Management information

Registered date

2025 Year 01 Month 13 Day

Last modified on

2026 Year 06 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064819