UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009111
Receipt number R000007591
Scientific Title Study of the effect of flurbiprofen for prevention of mesenteric traction syndrome.
Date of disclosure of the study information 2012/10/14
Last modified on 2017/10/21 19:14:13

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Basic information

Public title

Study of the effect of flurbiprofen for prevention of mesenteric traction syndrome.

Acronym

MTS trial

Scientific Title

Study of the effect of flurbiprofen for prevention of mesenteric traction syndrome.

Scientific Title:Acronym

MTS trial

Region

Japan


Condition

Condition

mesenteric traction syndrome (colorectal cancer)

Classification by specialty

Surgery in general Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate whether the mesenteric traction syndrome can be prevented by administration of flurbiprofen.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

The incidence of mesenteric traction syndrome

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Medicine

Interventions/Control_1

Administration of flurbiprofen axetil during induction of anesthesia

Interventions/Control_2

Administration of flurbiprofen axetil after the onset of mesenteric traction syndrome.

Interventions/Control_3

No preventive action

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

Elected abdominal colorectal surgery patients in our hospital

Key exclusion criteria

Liver dysfunction
Renal dysfunction
Gastroduodenal ulcer
Aspirin-induced asthma
Laparoscopic surgery

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hidemasa takahashi

Organization

Tokyo Metropolitan Bokutoh Hospital

Division name

Dept. anesthesiology

Zip code


Address

4-23-15,Kotobashi,Sumida-ku, Tokyo,130-8575,Japan

TEL

03-3633-6151

Email



Public contact

Name of contact person

1st name
Middle name
Last name Hidemasa takahashi

Organization

Tokyo Metropolitan Bokutoh Hospital

Division name

Dept. anesthesiology

Zip code


Address

4-23-15,Kotobashi,Sumida-ku, Tokyo,130-8575,Japan

TEL

03-3633-6151

Homepage URL


Email



Sponsor or person

Institute

Tokyo Metropolitan Bokutoh Hospital

Institute

Department

Personal name



Funding Source

Organization

Tokyo Metropolitan

Organization

Division

Category of Funding Organization

Local Government

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo

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

東京都立墨東病院(東京都)


Other administrative information

Date of disclosure of the study information

2012 Year 10 Month 14 Day


Related information

URL releasing protocol


Publication of results

Published


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

Completed

Date of protocol fixation

2011 Year 09 Month 22 Day

Date of IRB


Anticipated trial start date

2011 Year 10 Month 01 Day

Last follow-up date

2015 Year 12 Month 31 Day

Date of closure to data entry

2015 Year 12 Month 31 Day

Date trial data considered complete

2015 Year 12 Month 31 Day

Date analysis concluded

2015 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2012 Year 10 Month 14 Day

Last modified on

2017 Year 10 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007591


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name