UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027605
Receipt number R000031288
Scientific Title A comparison of clinical outcomes after ACL reconstruction using patellar tendon versus hamstring autograft
Date of disclosure of the study information 2017/07/01
Last modified on 2017/06/02 16:16:52

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Basic information

Public title

A comparison of clinical outcomes after ACL reconstruction using patellar tendon versus hamstring autograft

Acronym

A comparison of BTB vs STG for ACLR

Scientific Title

A comparison of clinical outcomes after ACL reconstruction using patellar tendon versus hamstring autograft

Scientific Title:Acronym

A comparison of BTB vs STG for ACLR

Region

Japan


Condition

Condition

Anterior cruciate ligament injury

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of the study is to compare the clinical outcomes in anterior cruciate ligament reconstruction between bone-patellar tendon-bone (BTB) versus hamstrings tendon (STG) grafts.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Stability of the knee joint

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

ACL reconstruction with bone-patellar tendon-bone(BTB)

Interventions/Control_2

Double-bundle ACL reconstruction with hamstrings(STG)

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

14 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Primary ACL reconstruction for isolated ACL injury

Key exclusion criteria

Bilateral ACL-injury, multiple ligament injury, and past injured/surgical history of the knee

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hideyuki Koga

Organization

Tokyo Medical and Dental University

Division name

Department of Joint Surgery and Sports Medicine

Zip code


Address

1-5-45 Yushima, Bunkyo-ku, Tokyo

TEL

03-5803-4020

Email

koga.orj@tmd.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masafumi Horie

Organization

Tokyo Medical and Dental University

Division name

Department of Joint Surgery and Sports Medicine

Zip code


Address

1-5-45 Yushima, Bunkyo-ku, Tokyo

TEL

03-5803-4775

Homepage URL


Email

horie.orj@tmd.ac.jp


Sponsor or person

Institute

Tokyo Medical and Dental University

Institute

Department

Personal name



Funding Source

Organization

Tokyo Medical and Dental 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


Address


Tel


Email



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 07 Month 01 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

Preinitiation

Date of protocol fixation

2017 Year 06 Month 02 Day

Date of IRB


Anticipated trial start date

2017 Year 08 Month 01 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry

2025 Year 03 Month 31 Day

Date trial data considered complete

2025 Year 03 Month 31 Day

Date analysis concluded

2026 Year 03 Month 30 Day


Other

Other related information



Management information

Registered date

2017 Year 06 Month 02 Day

Last modified on

2017 Year 06 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031288


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name