UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012133
Receipt number R000014165
Scientific Title The efficacy and safety of peripheral nerve block: a randomized controlled study
Date of disclosure of the study information 2013/10/29
Last modified on 2016/10/10 09:29:19

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Basic information

Public title

The efficacy and safety of peripheral nerve block: a randomized controlled study

Acronym

The efficacy and safety of peripheral nerve block: a randomized controlled study

Scientific Title

The efficacy and safety of peripheral nerve block: a randomized controlled study

Scientific Title:Acronym

The efficacy and safety of peripheral nerve block: a randomized controlled study

Region

Japan


Condition

Condition

Laparoscopic surgery

Classification by specialty

Anesthesiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Assess the efficacy and adverse effects of continuous peripheral nerve block in patients after laparoscopic surgery.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase



Assessment

Primary outcomes

Pain score
Affected area after block performance
Blood drug concentration
Elapsed time until first additional analgesia after surgery

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

0.5 % ropivacaine 30ml, rectus sheath block

Interventions/Control_2

0.5 % ropivacaine 30ml, transversus abdominis plane block

Interventions/Control_3

0.375 % ropivacaine 40ml, quadratus lumborum block

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

Patients (American Society of Anesthesiologists physical status I-III) scheduled for elective laparoscopic surgery under general anesthesia

Key exclusion criteria

Patients were excluded if they were younger than 18 years or older than 80 years of age, had a history of allergy to local anesthetics, had a history of neurological disorder affecting the corresponding limb, or were pregnant.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Soushi Iwasaki

Organization

Sapporo Medical University School of Medicine

Division name

Department of Anesthesiology

Zip code


Address

South 1 West 16 Chuo-ku, Sapporo, Hokkaido 060-8556, Japan

TEL

011-611-2111(ext.3568)

Email

iwasakis@sapmed.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takeshi Murouchi

Organization

Sapporo Medical University School of Medicine

Division name

Department of Anesthesiology

Zip code


Address

South 1 West 16 Chuo-ku, Sapporo, Hokkaido 060-8556, Japan

TEL

011-611-2111(ext.3568)

Homepage URL


Email

murouchi@sapmed.ac.jp


Sponsor or person

Institute

Sapporo Medical University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

none

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


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

札幌医科大学附属病院(北海道)


Other administrative information

Date of disclosure of the study information

2013 Year 10 Month 29 Day


Related information

URL releasing protocol


Publication of results

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

Completed

Date of protocol fixation

2013 Year 09 Month 19 Day

Date of IRB


Anticipated trial start date

2013 Year 10 Month 30 Day

Last follow-up date

2017 Year 12 Month 31 Day

Date of closure to data entry

2018 Year 01 Month 31 Day

Date trial data considered complete

2018 Year 01 Month 31 Day

Date analysis concluded

2018 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2013 Year 10 Month 27 Day

Last modified on

2016 Year 10 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014165


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name