UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018115
Receipt number R000020968
Scientific Title The effect of tranexamic acid on blood loss in bimaxillary orthognathic surgery.
Date of disclosure of the study information 2015/07/01
Last modified on 2020/12/25 17:51:36

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Basic information

Public title

The effect of tranexamic acid on blood loss in bimaxillary orthognathic surgery.

Acronym

The effect of tranexamic acid on blood loss in bimaxillary orthognathic surgery.

Scientific Title

The effect of tranexamic acid on blood loss in bimaxillary orthognathic surgery.

Scientific Title:Acronym

The effect of tranexamic acid on blood loss in bimaxillary orthognathic surgery.

Region

Japan


Condition

Condition

Jaw defomities

Classification by specialty

Oral surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine the efficacy of intraoperative treatment with tranexamic acid in reducing intraoperative blood loss in patients undergoing orthognathic surgery.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

intraoperative blood loss

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

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

A loading dose of 20mg/kg of tranexamic acid in infused intravenously before Le Fort 1 osteotomy.

Interventions/Control_2

A loading dose of 10mg/kg of tranexamic acid in infused intravenously before Le Fort 1 osteotomy and sagittal splitting ramus osteotomy.

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

16 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients older than 16 years old and undergoing orthognathic surgery agoreed to participate in this traial.

Key exclusion criteria

Exclusion criteria are atrial fibrillation, coronary artery disease treated with drug eluting stent, severe choronic renal failure, congenital or acquried thrombophillia, and known or suspected allergy to tranexamic acid.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Hideki
Middle name
Last name Ichikawa

Organization

Tokyo Metroplitan Ohtsuka Hospital

Division name

Department of Stomatology

Zip code

170-8476

Address

2-8-1 Minami-ohtsuka,Toshima-ku,Tokyo

TEL

03-3941-3211

Email

hideki_ichikawa@tmhp.jp


Public contact

Name of contact person

1st name Hideki
Middle name
Last name Ichikawa

Organization

Tokyo Metropolitan Ohtsuka Hospital

Division name

Depertment of Stomatology

Zip code

170-8476

Address

2-8-1 Minami-ohtsuka,Toshima-ku,Tokyo

TEL

03-3941-3211

Homepage URL


Email

hideki_ichikawa@tmhp.jp


Sponsor or person

Institute

Tokyo Metropolitan Ohtsuka Hospital

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

Tokyo Metropolitan Ohtsuka Hospital

Address

2-8-1 Minami-ohtsuka,Toshima-ku,Tokyo

Tel

03-3941-3211

Email

hideki_ichikawa@tmhp.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

東京都立大塚病院


Other administrative information

Date of disclosure of the study information

2015 Year 07 Month 01 Day


Related information

URL releasing protocol

https://doi.org/10.5927/jjjd.28.269

Publication of results

Partially published


Result

URL related to results and publications

https://doi.org/10.5927/jjjd.28.269

Number of participants that the trial has enrolled

99

Results

It has been suggested that TXA may be able to reduce intraoperative blood loss during orthognathic surgery.

Results date posted

2020 Year 12 Month 25 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results

2018 Year 12 Month 25 Day

Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2015 Year 05 Month 26 Day

Date of IRB

2015 Year 08 Month 01 Day

Anticipated trial start date

2015 Year 07 Month 01 Day

Last follow-up date

2020 Year 12 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 06 Month 27 Day

Last modified on

2020 Year 12 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020968


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name