UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029914
Receipt number R000034171
Scientific Title The efficacy of Quadratus Lumborum Block as a postoperative analgesia for Total Hip Arthroplasty.
Date of disclosure of the study information 2017/11/14
Last modified on 2021/08/07 15:27:27

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Basic information

Public title

The efficacy of Quadratus Lumborum Block as a postoperative analgesia for Total Hip Arthroplasty.

Acronym

The efficacy of Quadratus Lumborum Block as a postoperative analgesia for Total Hip Arthroplasty.

Scientific Title

The efficacy of Quadratus Lumborum Block as a postoperative analgesia for Total Hip Arthroplasty.

Scientific Title:Acronym

The efficacy of Quadratus Lumborum Block as a postoperative analgesia for Total Hip Arthroplasty.

Region

Japan


Condition

Condition

Hip osteoarthritis

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The strength maintenance of Hip joint after Quadratus Lumborum Block(QLB).

Basic objectives2

Others

Basic objectives -Others

Analgesic effect in postoperative period.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The muscle strength of hip flexion using by hand held dynamometer 6 hours after total hip arthroplasty.

Key secondary outcomes

Postoperative analgesic scores (0,6,12,24,48 hours), The muscle strength of hip flexion using by hand held dynamometer(0,12,24,48 hours), Complications. The effective are of QLB.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

QLB

Interventions/Control_2

Lumber Plexus Block(LPB)

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

75 years-old >

Gender

Male and Female

Key inclusion criteria

Initial total hip arthroplasty.

Key exclusion criteria

Blood platelet disorder, Coagulation intolerance. Difficulty to have a communicate.

Target sample size

58


Research contact person

Name of lead principal investigator

1st name Takafumi
Middle name
Last name Iida

Organization

Asahikawa Medical University

Division name

Anesthesiology and Critical Care Medicine

Zip code

0788510

Address

Midorigaoka-higashi 2-1-1-1,Asahikawa,Hokkaido,Japan

TEL

0166682583

Email

takka1845@fg7.so-net.ne.jp


Public contact

Name of contact person

1st name Takafumi
Middle name
Last name Iida

Organization

Asahikawa Medical University

Division name

Anesthesiology and Critical Care Medicine

Zip code

0788510

Address

Midorigaoka-higashi 2-1-1-1,Asahikawa,Hokkaido,Japan

TEL

0166682583

Homepage URL


Email

takka1845@fg7.so-net.ne.jp


Sponsor or person

Institute

Asahikawa medical university

Institute

Department

Personal name



Funding Source

Organization

Department of Anesthesiology and critical care medicine ,Asahikawa medical 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

Asahikawa Medical University

Address

Midorigaoka-higashi 2-1-1-1,Asahikawa,Hokkaido,Japan

Tel

0166682583

Email

pikaseika@jimu.asahikawa-med.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 11 Month 14 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

Terminated

Date of protocol fixation

2017 Year 09 Month 22 Day

Date of IRB

2017 Year 11 Month 10 Day

Anticipated trial start date

2017 Year 11 Month 20 Day

Last follow-up date

2021 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 11 Month 10 Day

Last modified on

2021 Year 08 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034171


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name