UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000041210
Receipt number R000047064
Scientific Title The immediate effect of a trigger point injection with local anesthetic affects the subsequent course of pain in myofascial pain syndrome in cancer patients
Date of disclosure of the study information 2020/07/26
Last modified on 2020/07/26 21:24:25

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Basic information

Public title

The immediate effect of a trigger point injection with local anesthetic affects the subsequent course of pain

Acronym

The immediate effect of a trigger point injection

Scientific Title

The immediate effect of a trigger point injection with local anesthetic affects the subsequent course of pain in myofascial pain syndrome in cancer patients

Scientific Title:Acronym

The immediate effect of a trigger point injection

Region

Japan


Condition

Condition

Myofascial pain syndrome

Classification by specialty

Anesthesiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To clarify how the effect of a decrease in pain immediately after TPI with local anesthetic affected the subsequent course of pain, and whether it increased expectations of a decrease in pain.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The primary outcome was a difference in the rate of patients with pain reduction at 7 days after TPI, between patients with and without a decrease in pain immediately after TPI.

Key secondary outcomes



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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Cancer patients who received TPI for MPS

Key exclusion criteria

(1) were younger than 20 years
(2) had any comorbidity relating to psychiatric diseases or conditions that made communication difficult, such as cognitive impairment

Target sample size

205


Research contact person

Name of lead principal investigator

1st name Hideaki
Middle name
Last name Hasuo

Organization

Kansai Medical University

Division name

Psychosomatic Medicine

Zip code

573-1010

Address

2-5-1-505, Shinmachi, Hirakata, Osaka

TEL

072-804-0101

Email

hasuohid@hirakata.kmu.ac.jp


Public contact

Name of contact person

1st name Hideaki
Middle name
Last name Hasuo

Organization

Kansai Medical University

Division name

Psychosomatic Medicine

Zip code

573-1010

Address

2-5-1-505, Shinmachi, Hirakata, Osaka

TEL

072-804-0101

Homepage URL


Email

hasuohid@hirakata.kmu.ac.jp


Sponsor or person

Institute

Kansai Medical University

Institute

Department

Personal name



Funding Source

Organization

Kansai Medical University

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kansai Medical University

Address

2-5-1-505, Shinmachi, Hirakata, Osaka

Tel

072-804-0101

Email

hasuohid@hirakata.kmu.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

2020 Year 07 Month 26 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

205

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

2018 Year 10 Month 01 Day

Date of IRB

2018 Year 12 Month 19 Day

Anticipated trial start date

2018 Year 12 Month 19 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Prospective, single-center, observational clinical trial


Management information

Registered date

2020 Year 07 Month 26 Day

Last modified on

2020 Year 07 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047064


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name