UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000021885
Receipt number R000025237
Scientific Title Is continuous transmuscular quadrates lumborum (QLB) block an effective perioperative analgesia for total hip arthroplasty?
Date of disclosure of the study information 2016/04/13
Last modified on 2020/02/21 06:28:33

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Basic information

Public title

Is continuous transmuscular quadrates lumborum (QLB) block an effective perioperative analgesia for total hip arthroplasty?

Acronym

An efficacy of continuous transmuscular QLB block for THA.

Scientific Title

Is continuous transmuscular quadrates lumborum (QLB) block an effective perioperative analgesia for total hip arthroplasty?

Scientific Title:Acronym

An efficacy of continuous transmuscular QLB block for THA.

Region

Japan


Condition

Condition

Total hip arthroplasty.

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

An efficacy of perioperative pain management for transmusucular QLB

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

the cumulative fentanyl (rescue analgesia) consumption during the first 48 hours post-surgery

Key secondary outcomes

1.the number of demanded and delivered fentanyl boluses
2. the number of patients with complications such as nausea and vomiting during the first 48 hours after surgery
3. sensory level by cold tests at awake situation


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) 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

Transmuscular QLB group

Interventions/Control_2

Lumbar plexus nerve block group

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

the patients planned a total hip arthroplasty

Key exclusion criteria

secondary surgery
Bilateral THA

Target sample size

72


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@yahoo.co.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@yahoo.co.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, ota-ku

Tel

03-3784-8575

Email

ueshimhi@yahoo.co.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

2016 Year 04 Month 13 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

72

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

2016 Year 04 Month 13 Day

Date of IRB

2016 Year 04 Month 13 Day

Anticipated trial start date

2016 Year 04 Month 13 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

2016 Year 04 Month 12 Day

Last modified on

2020 Year 02 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025237


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name