UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017483
Receipt number R000020265
Scientific Title Accuracy of Patient Specific Instrumentation in Total Knee Arthroplasty
Date of disclosure of the study information 2015/05/11
Last modified on 2022/11/14 10:34:45

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Basic information

Public title

Accuracy of Patient Specific Instrumentation in Total Knee Arthroplasty

Acronym

Accuracy of Patient Specific Instrumentation in Total Knee Arthroplasty

Scientific Title

Accuracy of Patient Specific Instrumentation in Total Knee Arthroplasty

Scientific Title:Acronym

Accuracy of Patient Specific Instrumentation in Total Knee Arthroplasty

Region

Japan


Condition

Condition

Osteoarthritis of the knee

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the accuracy of patient specific instrumentation in total knee arthroplasty

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

accuracy of postoperative alignment
accuracy of the intraoperative registration

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Use the patient specific instrumentation

Interventions/Control_2


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

the patients with osteoarthritis or rheumatoid arthritis who are need total knee arthroplasty

Key exclusion criteria

the patients with with inflammatory disease, trauma nor surgical history

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Ken
Middle name
Last name Okazaki

Organization

Kyushu University

Division name

Department of Orthopaedic Surgery

Zip code

812-8582

Address

3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

TEL

092-642-5488

Email

okazaki@ortho.med.kyushu-u.ac.jp


Public contact

Name of contact person

1st name Hideki
Middle name
Last name Mizu-uchi

Organization

Kyushu University

Division name

Department of Orthopaedic Surgery

Zip code

812-8582

Address

3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

TEL

092-642-5488

Homepage URL


Email

himizu@ortho.med.kyushu-u.ac.jp


Sponsor or person

Institute

Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University

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

Center for Clinical and Translational Research of Kyushu University Hospital

Address

3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

Tel

092-642-5774

Email

tr-info@med.kyushu-u.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

2015 Year 05 Month 11 Day


Related information

URL releasing protocol

https://pubmed.ncbi.nlm.nih.gov/28888738/

Publication of results

Published


Result

URL related to results and publications

https://pubmed.ncbi.nlm.nih.gov/28888738/

Number of participants that the trial has enrolled

18

Results

Article was published

Results date posted

2022 Year 11 Month 14 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

18 knees

Participant flow

no problem

Adverse events

none

Outcome measures

radiological outcome
functional outcome

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2013 Year 11 Month 11 Day

Date of IRB

2013 Year 11 Month 11 Day

Anticipated trial start date

2013 Year 11 Month 12 Day

Last follow-up date

2017 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

2015 Year 05 Month 10 Day

Last modified on

2022 Year 11 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020265


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name