UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019751
Receipt number R000022801
Scientific Title Prospective study of predictor for efficiency of treatment with Nintedanib for idiopathic pulmonary fibrosis
Date of disclosure of the study information 2015/11/11
Last modified on 2019/11/15 15:43:50

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Basic information

Public title

Prospective study of predictor for efficiency of treatment with Nintedanib for idiopathic pulmonary fibrosis

Acronym

Study of predictor for treatment with Nintedanib

Scientific Title

Prospective study of predictor for efficiency of treatment with Nintedanib for idiopathic pulmonary fibrosis

Scientific Title:Acronym

Study of predictor for treatment with Nintedanib

Region

Japan


Condition

Condition

idiopathic pulmonary fibrosis

Classification by specialty

Pneumology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Analysis of biomarker for efficiency of treatment with Nintedanib for idiopathic pulmonary fibrosis

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

The correlation between serum periostin level and change of pulmonary function

Key secondary outcomes

1. The correlation between serum periostin level and clinical data except for pulmonary function
2. Predictors of overall survival and progression-free-survival


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

40 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

The case with idiopathic pulmonary fibrosis who visited to the hospitals participated to this study.
Patients who fulfilled all of the following criteria
1. Age is more than 40 years old.
2. After receiving enough explanations about participation in the study, there was the document consent by free will of patients thorough his enough understanding.
3. Patient who was diagnosed as idiopathic pulmonary fibrosis by criteria of this study
4. Disease activity is stable at registration
5. Patient who need treatment with nintedanib
6. Patient who can be treated with nintedanib within 2 weeks from obtaining informed consent

Key exclusion criteria

The patients who fulfilled one of the following criteria
1. Pregnant women.
2. Patient who was determined as ineligible by the investigator or the subinvestigator.
3. Patients treated with the following drug at the start of observation.
Corticosteroid (more than 10 mg per day in term of prednizolone)
Immunosuppressant
N-acetylcysteine
Pirfenidone
Study drug for idiopathic pulmonary fibrosis
4. Case with exclusion disease

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Tomoaki
Middle name
Last name Hoshino

Organization

Kurume University, School of Medicine

Division name

Division of Respirology, Neurology and Rheumotology, Department of Internal Medicine

Zip code

8300011

Address

Asahi-machi 67, Kurume, Japan

TEL

81-942-31-7560

Email

hoshino@med.kurume-u.ac.jp


Public contact

Name of contact person

1st name Masaki
Middle name
Last name Okamoto

Organization

Kurume University, School of Medicine

Division name

Division of Respirology, Neurology and Rheumotology, Department of Internal Medicine

Zip code

8300011

Address

Asahi-machi 67, Kurume, Japan

TEL

81-942-31-7560

Homepage URL


Email

okamoto_masaki@med.kurume-u.ac.jp


Sponsor or person

Institute

Kurume University, School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Division of Respirology, Neurology and Rheumotology, Department of Internal Medicine, Kurume University, School of Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Department of Radiology and Center for Diagnostic Imaging, Kurume University, School of Medicine
Department of Radiology, Kinki Central Hospital of the Mutual Aid Association of Public School Teachers
Second Department of Internal Medicine, Nagasaki University, School of Medicine
Department of Pathology, Nagasaki University, School of Medicine
Department of Respiratory Medicine and Allergy, Tosei General Hospital
Department of Respiratory Medicine, Graduate School of Medicine, Osaka City University
Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine
Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center
Kirigaoka Tsuda Hospital
The First Department of Internal Medicine, Shinshu University School of Medicine
Division of Pathology, Saitama Cardiovascular Respiratory Centre
Department of Respiratory Medicine and Infectious Diseases, Oita University Faculty of Medicine
Japan Community Health care Organization (JCHO) Kurume General Hospital
Institute for Advancement of Clinical and Translational Science, Kyoto University School of Medicine

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Academic Research Organization of Kurume University

Address

Asahi-machi 67, Kurume, Fukuoka

Tel

0942-35-3311

Email

i_rinri@kurume-u.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

久留米大学病院 (福岡県)
長崎大学病院 (長崎県)
産業医科大学 (福岡県)
公立陶生病院 (愛知県)
大阪市立大学病院 (大阪府)
札幌医科大学病院 (北海道)
神奈川県立循環器呼吸器病センター (神奈川県)
信州大学病院 (長野県)
大分大学病院 (大分県)
九州大学病院 (福岡県)
広島大学病院 (広島県)
天理よろづ相談所病院 (奈良県)
国立病院機構東京病院 (東京都)
NHO近畿中央胸部疾患センター (大阪府)
浜松医科大学 (静岡県)
東邦大学医療センター大森病院 (東京都)
獨協医科大学 (栃木県)
NHO茨城東病院 (茨城県)
富山大学附属病院 (富山県)
沖縄県立中部病院 (沖縄県)
順天堂大学医学部 (東京都)
京都大学病院 (京都府)
福島県立医科大学 (福島県)
高知大学病院 (高知県)
東京医科歯科大学 (東京都)
福岡大学病院 (福岡県)
日本医科大学病院 (東京都)
北海道大学病院 (北海道)


Other administrative information

Date of disclosure of the study information

2015 Year 11 Month 11 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

95

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

No longer recruiting

Date of protocol fixation

2015 Year 10 Month 13 Day

Date of IRB

2015 Year 08 Month 11 Day

Anticipated trial start date

2015 Year 11 Month 11 Day

Last follow-up date

2020 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This study was a cohort study to analyze the clinical data and preserve sera.

Study design
Prospective cohort study

Subjects
Patients with idiopathic pulmonary
fibrosis who visited collaborative study
hospitals from November 2015 until
September 2018

Measuring substance
Serum levels of periostin



Management information

Registered date

2015 Year 11 Month 11 Day

Last modified on

2019 Year 11 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022801


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name