UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030996
Receipt number R000034979
Scientific Title Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty
Date of disclosure of the study information 2018/01/25
Last modified on 2021/10/01 08:56:43

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Basic information

Public title

Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty

Acronym

Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty

Scientific Title

Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty

Scientific Title:Acronym

Comparison of ultrasound guided femoral nerve block and adductor canal block for postoperative analgesia after total knee arthroplasty

Region

Japan


Condition

Condition

patients receiving bilateral total knee arthroplasty

Classification by specialty

Orthopedics Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We compare femoral nerve block and adductor canal block for influence on postoperative analgesia and rehabilitation after bilateral TKA.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Phase III


Assessment

Primary outcomes

Postoperative 24h Numerical Rating Scale(NRS) at rest

Key secondary outcomes

Postoperative NRS at rest (0,6,12,48h)
Postoperative NRS during knee movement (0,6,12,24,48h)
Postoperative Range of Motion (ROM)(12,24,48h)
Postoperative effect of Sciatic nerve block (0,12,24h)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -investigator(s) and 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

Femoral nerve block

Interventions/Control_2

Adductor canal 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

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients scheduled bilateral total knee arthroplasty

Key exclusion criteria

history of complications
Patients who can not evaluate NRS
Patients with local anesthetics allergy

Target sample size

46


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

kyokui090018@gmail.com


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

kyokui090018@gmail.com


Sponsor or person

Institute

Asahikawa Medical University
Anesthesiology and Critical Care Medicine

Institute

Department

Personal name



Funding Source

Organization

Asahikawa Medical University
Anesthesiology and Critical Care Medicine

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

Asahkawa Medical University

Address

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

Tel

0166682297

Email

rs-kk.g@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

2018 Year 01 Month 25 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 10 Month 20 Day

Date of IRB

2017 Year 10 Month 27 Day

Anticipated trial start date

2017 Year 11 Month 20 Day

Last follow-up date

2022 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 01 Month 25 Day

Last modified on

2021 Year 10 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034979


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name