UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013750
Receipt number R000016046
Scientific Title Study on effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis
Date of disclosure of the study information 2014/04/21
Last modified on 2015/04/17 09:35:29

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Basic information

Public title

Study on effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis

Acronym

Study on effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis

Scientific Title

Study on effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis

Scientific Title:Acronym

Study on effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis

Region

Japan


Condition

Condition

Rheumatoid arthritis, Periodontitis

Classification by specialty

Clinical immunology Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of the present study is to evaluate clinically and biologically the effects of cytokine targeted therapy on periodontal condition in patients with rheumatoid arthritis.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Gingival index
Bleeding on probing
Probing pocket depth
Clinical attachment level

Key secondary outcomes

Serum markers
hsCRP
IL-6
TNF-alpha
MMP-3


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

IL-6 receptor inhibition group:
Tocilizumab will be infused in 20 patients, and its effectiveness will be evaluated at 3 and 6 months later.

Interventions/Control_2

TNF inhibition group:
Infliximab, Etanercept, and Adalimumab will be infused in 20 patients, and its effectiveness will be evaluated at 3 and 6 months later.

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

1. Individuals whose consents are obtained in written form on participation in the present study.
2. Individuals with rheumatoid arthritis who have a minimum of 20 teeth.

Key exclusion criteria

1.Individuals who had received scaling and root planing within the previous 3 months before the study starts.
2.Individuals who had taken systemic antibiotics or anti-inflammatory drugs within 3 months before the study starts.
3.Individuals with severe systemic diseases
4.Individuals who are or suspected to be pregnant.
5.Individuals who are considered not eligible for the present study due to any reasons by the investigators.

Target sample size

80


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiromasa Yoshie

Organization

Niigata University Graduate School of Medical and Dental Sciences

Division name

Division of Periodontology

Zip code


Address

2-5274, Gakkocho-dori, Chuo-ku, Niigata, 951-8514, Japan

TEL

025-227-2869

Email

yoshie@dent.niigata-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tetsuo Kobayashi

Organization

Niigata University Medical and Dental Hospital

Division name

General Dentistry and Clinical Education Unit

Zip code


Address

2-5274, Gakkocho-dori, Chuo-ku, Niigata, 951-8514, Japan

TEL

025-227-2870

Homepage URL


Email

kotetsuo@dent.niigata-u.ac.jp


Sponsor or person

Institute

Division of Periodontology, Niigata University Graduate School of Medical and Dental Sciences

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

Japan


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

新潟大学大学院医歯学総合研究科(新潟県)、新潟県立リウマチセンター(新潟県)


Other administrative information

Date of disclosure of the study information

2014 Year 04 Month 21 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

2011 Year 07 Month 12 Day

Date of IRB


Anticipated trial start date

2011 Year 07 Month 31 Day

Last follow-up date

2015 Year 03 Month 31 Day

Date of closure to data entry

2015 Year 03 Month 31 Day

Date trial data considered complete

2015 Year 04 Month 30 Day

Date analysis concluded

2015 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2014 Year 04 Month 17 Day

Last modified on

2015 Year 04 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016046


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name