UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000052485
Receipt number R000059902
Scientific Title A trial to predict of pain treatment progress with questionnaires and visual analogue scale.
Date of disclosure of the study information 2023/10/13
Last modified on 2023/10/13 13:42:03

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

A trial to predict of pain treatment progress with questionnaires and visual analogue scale.

Acronym

To predict of pain treatment progress with questionnaires and VAS.

Scientific Title

A trial to predict of pain treatment progress with questionnaires and visual analogue scale.

Scientific Title:Acronym

To predict of pain treatment progress with questionnaires and VAS.

Region

Japan


Condition

Condition

Various pain

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To study to find specific patterns of questionnaire scores and VAS in the first visit to predict of pain treatment progress and/or to choice useful treatment measures.

Basic objectives2

Others

Basic objectives -Others

To predict of pain treatment progress with VAS and questionnaires

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Relationship between the change of VAS with treatment progress and questionnaires scores in the first visit.

Key secondary outcomes

Relationship between questionnaire scores and change of VAS three months after the first visit.


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Pain patients

Key exclusion criteria

Patients who could not answer questionnaires and VAS.

Target sample size

1679


Research contact person

Name of lead principal investigator

1st name Osamu
Middle name
Last name Nishida

Organization

Fujita Health University School of Medicine

Division name

Department of Anesthesiology and Critical Care Medicine

Zip code

470-1192

Address

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, Japan

TEL

0562-93-2925

Email

nishida@fujita-hu.ac.jp


Public contact

Name of contact person

1st name Junpei
Middle name
Last name Shibata

Organization

Fujita Health University Okazaki Medical Center

Division name

Department of Anesthesiology

Zip code

444-0827

Address

1 Gotanda, Harisaki-cho, Okazaki-shi, Aichi, Japan

TEL

0564-64-8800

Homepage URL


Email

shibata@fujita-hu.ac.jp


Sponsor or person

Institute

Fujita Health University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Fujita Health University School of Medicine Department of Anesthesiology and Critical Care Medicine

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Review Committee of Fujita Health University

Address

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, Japan

Tel

0562-93-2865

Email

f-irb@fujita-hu.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



Other administrative information

Date of disclosure of the study information

2023 Year 10 Month 13 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

1679

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

2023 Year 06 Month 30 Day

Date of IRB

2023 Year 07 Month 11 Day

Anticipated trial start date

2023 Year 07 Month 11 Day

Last follow-up date

2028 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To study to find specific patterns of questionnaire scores and VAS in the first visit to predict of pain treatment progress and/or to choice useful treatment measures.


Management information

Registered date

2023 Year 10 Month 13 Day

Last modified on

2023 Year 10 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000059902


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name