UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000033481
Receipt number R000038173
Scientific Title Efficacy of Erector Spinae Plane block for lumbar spine surgery :prospective study:
Date of disclosure of the study information 2018/07/23
Last modified on 2018/07/23 16:44:10

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Basic information

Public title

Efficacy of Erector Spinae Plane block for lumbar spine surgery :prospective study:

Acronym

Efficacy of ESP block for lumbar spine surgery

Scientific Title

Efficacy of Erector Spinae Plane block for lumbar spine surgery :prospective study:

Scientific Title:Acronym

Efficacy of ESP block for lumbar spine surgery

Region

Japan


Condition

Condition

lumbar spine disease

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

prospective study of postoperative analgesic efficacy of erector spinae plane block

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

amount of additional bolus fentanyl from intravenous patient-controlled-analgesia at 24 hour after operation

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine Maneuver

Interventions/Control_1

after general anesthesia induction, injecting 40 ml of 0.25% levobupivacaine as erector spinae plane block

Interventions/Control_2

after general anesthesia induction, injecting 40 ml of natural saline in area of erector spinae plane block

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

patient scheduled lumbar spine surgery at Showa university hospital
patient who agree with the study

Key exclusion criteria

past history of lumbar spine surgery
scheduled emergency lumbar spine surgery
allergy with local anesthesia
hepatic or renal abnormality in blood test
regarded as unfit by examination doctor

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hironobu Ueshima

Organization

Showa university

Division name

department of anesthesiology

Zip code


Address

1-5-8, Hatanodai Shinagawa-ku Tokyo

TEL

03-3784-8000

Email

ueshimhi@med.showa-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Mayumi Inagaki

Organization

Showa university

Division name

department of anesthesiology

Zip code


Address

1-5-8, Hatanodai Shinagawa-ku Tokyo

TEL

03-3784-8000

Homepage URL


Email

mymhtt0120@gmail.com


Sponsor or person

Institute

Showa university

Institute

Department

Personal name



Funding Source

Organization

Showa university

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


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

昭和大学病院


Other administrative information

Date of disclosure of the study information

2018 Year 07 Month 23 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

2018 Year 07 Month 23 Day

Date of IRB


Anticipated trial start date

2018 Year 07 Month 23 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 07 Month 23 Day

Last modified on

2018 Year 07 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000038173


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name