UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015670
Receipt number R000018212
Scientific Title Efficacy of epidural administration of ant-TNF-alfa and anti-interleukin-6 receptor antibody onto spinal nerve for treatment of sciatica.
Date of disclosure of the study information 2014/11/12
Last modified on 2014/11/12 11:06:17

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Basic information

Public title

Efficacy of epidural administration of ant-TNF-alfa and anti-interleukin-6 receptor antibody onto spinal nerve for treatment of sciatica.

Acronym

Anti-Cytokine therapy for radicular pain (ACTRP)

Scientific Title

Efficacy of epidural administration of ant-TNF-alfa and anti-interleukin-6 receptor antibody onto spinal nerve for treatment of sciatica.

Scientific Title:Acronym

Anti-Cytokine therapy for radicular pain (ACTRP)

Region

Japan


Condition

Condition

low back and radicular leg pain caused by spinal stenosis were investigated.

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of the current study is to examine the effect of the anti-TNF-alfa and IL-6 receptor monoclonal antibodyon radicular pain by its epidural administration onto spinal nerves in patients with lumbar spinal stenosis.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Pain relief
side effect

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Double blind -all involved are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

1% Xylocaine

Interventions/Control_2

1% Xylocaine + anti-TNF-alfa receptor antibody

Interventions/Control_3

1% Xylocaine + anti-interleukin-6 receptor antibody

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

85 years-old >

Gender

Male and Female

Key inclusion criteria

1 Patients with low back pain, leg pain, or intermittent claudication
2 patients with pain that can beexplained X-ray, CT, MRIand discography.

Key exclusion criteria

1 Patients with impaired consciousness
2 Patients with severe heart failure, renal failure, liver failure and systemic complications such as respiratory failure.

Target sample size

90


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Seiji Ohtori

Organization

Graduate School of Medicine, Chiba University

Division name

Dept. of Orthopaedic Surgery

Zip code


Address

1-8-1 Inohana Chuo-ku, Chiba city, Chiba, Japan.

TEL

043-226-2117

Email

sohotri@faculty.chiba-u.jp


Public contact

Name of contact person

1st name
Middle name
Last name Seiji Ohtori

Organization

Graduate School of Medicine, Chiba University

Division name

Orthopaedic Surgery

Zip code


Address

1-8-1 Inohana Chuo-ku, Chiba city, Chiba, Japan.

TEL

043-226-2117

Homepage URL


Email

sohotri@faculty.chiba-u.jp


Sponsor or person

Institute

Dept. of Orthopaedic Surgery, Graduate School of Medicine, Chiba University

Institute

Department

Personal name



Funding Source

Organization

Uehara Memorial Foundation Research Grant

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



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



Other administrative information

Date of disclosure of the study information

2014 Year 11 Month 12 Day


Related information

URL releasing protocol


Publication of results

Partially published


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

Open public recruiting

Date of protocol fixation

2010 Year 08 Month 02 Day

Date of IRB


Anticipated trial start date

2014 Year 11 Month 12 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 11 Month 12 Day

Last modified on

2014 Year 11 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018212


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name