UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000032988
Receipt number R000037617
Scientific Title The comparison of analgesia and quadriceps strength between intermittent bolus and continuous technique for femoral nerve block after total knee arthroplasty
Date of disclosure of the study information 2018/07/15
Last modified on 2020/12/16 10:28:08

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Basic information

Public title

The comparison of analgesia and quadriceps strength between intermittent bolus and continuous technique for femoral nerve block after total knee arthroplasty

Acronym

The comparison of analgesia and quadriceps strength between intermittent bolus and continuous technique for femoral nerve block after total knee arthroplasty

Scientific Title

The comparison of analgesia and quadriceps strength between intermittent bolus and continuous technique for femoral nerve block after total knee arthroplasty

Scientific Title:Acronym

The comparison of analgesia and quadriceps strength between intermittent bolus and continuous technique for femoral nerve block after total knee arthroplasty

Region

Japan


Condition

Condition

Knee osteoarthritis

Classification by specialty

Orthopedics Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We compare between intermittent bolus and continuous technique of femoral nereve block for postoperative analgesia after total knee arthroplasty.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

analgesia after total knee arthroplasty

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

automated intermittent bolus technique

Interventions/Control_2

continuous technique

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with knee osteoarthritis who will undergo tatal knee arthroplasty

Key exclusion criteria

Patients with sever liver dysfunction, ranal failure, dementia or mental disorder

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Hiromi
Middle name
Last name Yoshinuma

Organization

Kameda Medical Center

Division name

Department of Anesthesiology

Zip code

2968602

Address

929 Higashi-cho, Kamogawa, Chiba, Japan

TEL

0470922211

Email

yoshinuma.hiromi@kameda.jp


Public contact

Name of contact person

1st name Hiromi
Middle name
Last name Yoshinuma

Organization

Kameda Medical Center

Division name

Department of Anesthesiology

Zip code

2968602

Address

929 Higashi-cho, Kamogawa, Chiba,Japan

TEL

0470922211

Homepage URL


Email

yoshinuma.hiromi@kameda.jp


Sponsor or person

Institute

Kameda Medical Center
Department of Anesthesiology

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

Kameda medical Center

Address

929 Higashicho, kamogawa, Chiba, Japan

Tel

0470922211

Email

clinical_research@kameda.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 07 Month 15 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

53

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

No longer recruiting

Date of protocol fixation

2014 Year 04 Month 22 Day

Date of IRB

2014 Year 04 Month 22 Day

Anticipated trial start date

2014 Year 05 Month 01 Day

Last follow-up date

2016 Year 04 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 06 Month 14 Day

Last modified on

2020 Year 12 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000037617


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name