UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000028679
Receipt number R000032832
Scientific Title Effectiveness of acetaminophen for rebound pain
Date of disclosure of the study information 2017/08/15
Last modified on 2019/08/17 09:07:32

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Basic information

Public title

Effectiveness of acetaminophen for rebound pain

Acronym

Effectiveness of acetaminophen for rebound pain

Scientific Title

Effectiveness of acetaminophen for rebound pain

Scientific Title:Acronym

Effectiveness of acetaminophen for rebound pain

Region

Japan


Condition

Condition

Fractures of the upper limbs

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Effectiveness

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

the number of requested PCA dose delivered at 24 hours post procedure

Key secondary outcomes

the number of pushed PCA dose delivered at 24 hours post procedure


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

No therapy

Interventions/Control_2

regular acetaminophen

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

the patients performed supraclavicular approach brachial plexus block for upper limbs fracture

Key exclusion criteria

1) less than 50kg
2) the patients performed uneffective brachial plexus block
3)tha patients who have renal or liver dysfunction

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Hironobu
Middle name
Last name Ueshima

Organization

Showa university hospital

Division name

Anesthesiology

Zip code

142-8666

Address

1-5-8, hatanodai, shinagawa-ku, tokyo

TEL

03-3784-8575

Email

ueshimhi@med.showa-u.ac.jp


Public contact

Name of contact person

1st name Hironobu
Middle name
Last name Ueshima

Organization

Showa university hospital

Division name

Anesthesiology

Zip code

142-8666

Address

1-5-8, hatanodai, shinagawa-ku, tokyo

TEL

03-3784-8575

Homepage URL


Email

ueshimhi@med.showa-u.ac.jp


Sponsor or person

Institute

Showa university hospital

Institute

Department

Personal name



Funding Source

Organization

Showa university hospital

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Showa university hospital

Address

1-5-8, hatanodai, shinagawa-ku, tokyo

Tel

03-3784-8575

Email

ueshimhi@med.showa-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



Other administrative information

Date of disclosure of the study information

2017 Year 08 Month 15 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

Preinitiation

Date of protocol fixation

2017 Year 08 Month 15 Day

Date of IRB

2017 Year 08 Month 15 Day

Anticipated trial start date

2017 Year 08 Month 15 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 08 Month 15 Day

Last modified on

2019 Year 08 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032832


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name