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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	JPRN
Last refreshed on:	17 October 2023
Main ID:	JPRN-UMIN000014311
Date of registration:	24/06/2014
Prospective Registration:	Yes
Primary sponsor:	Institute of Health Biosciences, The University of Tokushima Graduate School
Public title:	Examination of the clinical remission and functional remission in Infliximab using the increase-in-quantity protocol to TNF-alpha inhibitory drug resistance rheumatoid arthritis
Scientific title:	Examination of the clinical remission and functional remission in Infliximab using the increase-in-quantity protocol to TNF-alpha inhibitory drug resistance rheumatoid arthritis - Examination of the clinical remission and functional remission in Infliximab using an increase-in-quantity protocol
Date of first enrolment:	2014/06/24
Target sample size:	10
Recruitment status:	Pending
URL:	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016664
Study type:	Interventional
Study design:	Single arm Non-randomized
Phase:	Not selected

Countries of recruitment
Japan

Contacts

Name:	Yasuhiko Nishioka
Address:	3-18-15 Kuramoto-cho, Tokushima Japan
Telephone:	088-633-3111
Email:	yasuhiko@tokushima-u.ac.jp
Affiliation:	Institute of Health Biosciences, The University of Tokushima Graduate School Department of Respiratory Medicine and Rheumatology

Name:	Jun Kishi
Address:	3-18-15 Kuramoto-cho, Tokushima Japan
Telephone:	088-633-3111
Email:	kishijun@clin.med.tokushima-u.ac.jp
Affiliation:	Institute of Health Biosciences, Department of Respiratory Medicine and Rheumatology

Key inclusion & exclusion criteria

Inclusion criteria:
Exclusion criteria: 1)The patient who cannot use MTX 2)The patient who cannot use Infliximab 3)THe patient who ever used Infliximab

Age minimum: 20years-old
Age maximum: 75years-old
Gender: Male and Female

Health Condition(s) or Problem(s) studied

rheumatoid arthritis

Intervention(s)

The quantity of Infliximab is increased.

Primary Outcome(s)

clinical remission and functional remission

Secondary Outcome(s)

Secondary ID(s)

Source(s) of Monetary Support

Institute of Health Biosciences, The University of Tokushima Graduate School

Secondary Sponsor(s)

Ethics review

Status: YES
Approval date:
Contact:

Results

Results available:
Date Posted:
Date Completed:
URL:

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