UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000012354
Receipt No. R000014442
Official scientific title of the study Evaluation of the usefulness of ultrasound for ulcerative colitis
Date of disclosure of the study information 2013/11/22
Last modified on 2019/01/05 (Ver. 9)

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Basic information
Official scientific title of the study Evaluation of the usefulness of ultrasound for ulcerative colitis
Title of the study (Brief title) Evaluation of the usefulness of ultrasound for ulcerative colitis
Region
Japan

Condition
Condition ulcerative colitis
Classification by specialty
Gastroenterology Radiology
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To establish ultrasound for ulcerative colitis by comparing and verifying between ultrasound, endoscopy, and biopsy findings.
Basic objectives2 Others
Basic objectives -Others Establishment of diagnostic method
Trial characteristics_1 Exploratory
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Concordance rate between ultrasound finding (US grade) and endoscopic finding (Matts grade) in ulcerative colitis
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 Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 1
Purpose of intervention Diagnosis
Type of intervention
Medicine
Interventions/Control_1 Patients who give a written informed consent undergo contrast ultrasound by intravenous enhancer
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 Ulcerative colitis patients aged over 20 years-old who give a written informed consent.
Key exclusion criteria Patients who cannot undergo endoscopy and ultrasound safely.
Patients who are disqualified for the study by their physicians.
Target sample size 120

Research contact person
Name of lead principal investigator Takehiko Katsurada
Organization Hokkaido University Hospital
Division name Division of Gastroenterology and Hepatorogy
Address N14,W5,Kita-ku,Sapporo,Hokkaido
TEL 011-716-1161
Email tkatsu@amber.plala.or.jp

Public contact
Name of contact person Midori Nishioka
Organization Hokkaido University Hospital
Division name Institutional Review Board
Address Kita14 Nishi5, Kita-ku, Sapporo,Japan
TEL 011-706-7636
Homepage URL
Email crjimu@huhp.hokudai.ac.jp

Sponsor
Institute Department of Gastroenterology and Hepatology, Hokkaido University Hospital
Institute
Department

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)

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
2013 Year 11 Month 22 Day

Progress
Recruitment status Completed
Date of protocol fixation
2013 Year 10 Month 17 Day
Anticipated trial start date
2013 Year 11 Month 22 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Published
URL releasing results
Results
Other related information

Management information
Registered date
2013 Year 11 Month 19 Day
Last modified on
2019 Year 01 Month 05 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000014442