UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036670
Receipt number R000041785
Scientific Title A randomized analysis for subcuticular sutures versus staples for skin closure after liver resection
Date of disclosure of the study information 2019/05/08
Last modified on 2020/11/07 12:49:38

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Basic information

Public title

A randomized analysis for subcuticular sutures versus staples for skin closure after liver resection

Acronym

Methods for skin closure after liver resection

Scientific Title

A randomized analysis for subcuticular sutures versus staples for skin closure after liver resection

Scientific Title:Acronym

RCT for skin closure after liver resection

Region

Japan


Condition

Condition

Require for liver resection

Classification by specialty

Surgery in general Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Subcuticular sutures is known as a prefer for infectious complication after surgery. We planned to assess the infection rate between subcuticular sutures and staples for skin closure after liver resection.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Infectious complication of the surgical wound.

Key secondary outcomes

total infection rate, terms of administration and total medical cost


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration

Institution is considered as adjustment factor in dynamic allocation.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment Maneuver

Interventions/Control_1

Subcuticular sutures

Interventions/Control_2

staples for skin closure

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Require liver resection
2) entire treatment case
3) no other other resection but for gull bladder
4) EGOG PS 0-2
5) No co-morbidity for operation
6) Enough liver functional reserve
7) more than 20Y

Key exclusion criteria

1) No other abdominal surgery within 1 month.
2) No OMI or unstable angina within 6 month.
3) No idiopathic pneumonia or severe fibrosis of lung
4) Allergic reaction for operation materials
5) Stable psychologic status
6) Under pregnancy
7) Emergency operation
8) judged as "no inclusion" by the treatment doctors

Target sample size

530


Research contact person

Name of lead principal investigator

1st name SHINTARO
Middle name
Last name YAMAZAKI

Organization

Nihon university school of medicine

Division name

Digestive surgery

Zip code

1738610

Address

30-1 Ohyaguchkamicho Itabashiku Tokyo Japan

TEL

0339728111

Email

yamazaki-nmed@umin.ac.jp


Public contact

Name of contact person

1st name SHINTARO
Middle name
Last name YAMAZAKI

Organization

Nihon university school of medicine

Division name

Digestive surgery

Zip code

1738610

Address

30-1 Ohyaguchkamicho Itabashiku Tokyo Japan

TEL

0339728111

Homepage URL


Email

yamazaki-nmed@umin.ac.jp


Sponsor or person

Institute

Nihon university school of medicine

Institute

Department

Personal name



Funding Source

Organization

No funding in this study

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

Nihon university school of medicine

Address

30-1 Ohyaguchkamicho Itabashiku Tokyo Japan

Tel

0339728111

Email

yamazaki-nmed@umin.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

2019 Year 05 Month 08 Day


Related information

URL releasing protocol

none

Publication of results

Partially published


Result

URL related to results and publications

none

Number of participants that the trial has enrolled

560

Results

As the primary outcome, the wound complication rate did not differ significantly. As the secondary endpoint the wound complication rate in repeat resection significantly less frequent in subcuticular suture.

Results date posted

2020 Year 05 Month 08 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

common liver resection without biliary reconstruction.

Participant flow

Of the 581 enrolled patients, 281 patients with subcuticular sutures and 283 patients with staples were analysed.

Adverse events

None

Outcome measures

Primary: total wound complication.
Secondary: wound complication in repeat resection.

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2016 Year 12 Month 15 Day

Date of IRB

2017 Year 02 Month 15 Day

Anticipated trial start date

2017 Year 02 Month 16 Day

Last follow-up date

2019 Year 02 Month 15 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2019 Year 05 Month 08 Day

Last modified on

2020 Year 11 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041785


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name