UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013926
Receipt number R000016240
Scientific Title a study of tissue adhesive (DERMABOND TM) in transumbilical approach for laparo-endoscopic surgery
Date of disclosure of the study information 2014/05/12
Last modified on 2020/08/20 18:20:48

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Basic information

Public title

a study of tissue adhesive (DERMABOND TM) in transumbilical approach for laparo-endoscopic surgery

Acronym

a study of tissue adhesive (DERMABOND TM) in transumbilical approach for laparo-endoscopic surgery

Scientific Title

a study of tissue adhesive (DERMABOND TM) in transumbilical approach for laparo-endoscopic surgery

Scientific Title:Acronym

a study of tissue adhesive (DERMABOND TM) in transumbilical approach for laparo-endoscopic surgery

Region

Japan


Condition

Condition

adrenal tumor

Classification by specialty

Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to declear whether there is a significant difference by using DERMABOND TM in transumbilical laparo-endoscopic surgery

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

QOL

Key secondary outcomes



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


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

use of DERMABOND TM

Interventions/Control_2

control

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. patient who can understand this study and decided to join this study
2. patient who will undergo transumbilical laparo-endoscopic surgery

Key exclusion criteria

1. patient who have skin disease
2. patient who have metal allergy
3. patient who have experienced skin troubles by tape

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Mototsugu
Middle name
Last name Oya

Organization

Keio University School of Medicine

Division name

Department of Urology

Zip code

1600016

Address

35 Shinanomachi, Shinjuku, Tokyo

TEL

03-3353-1211

Email

moto-oya@z3.keio.jp


Public contact

Name of contact person

1st name Kazuhiro
Middle name
Last name Matsumoto

Organization

Keio University School of Medicine

Division name

Department of Urology

Zip code

1600016

Address

35 Shinanomachi, Shinjuku, Tokyo

TEL

03-3353-1211

Homepage URL


Email

kazz_matsumoto@yahoo.co.jp


Sponsor or person

Institute

Department of Urology, Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Department of Urology, Keio University School of Medicine

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

Department of Urology, Keio University School of Medicine

Address

35 Shinanomachi, Shinjuku, Tokyo

Tel

03-3353-1211

Email

yabuyobi@gmail.com


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

2014 Year 05 Month 12 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

36

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

2014 Year 05 Month 12 Day

Date of IRB

2014 Year 04 Month 28 Day

Anticipated trial start date

2014 Year 05 Month 12 Day

Last follow-up date

2020 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2018 Year 06 Month 30 Day


Other

Other related information



Management information

Registered date

2014 Year 05 Month 12 Day

Last modified on

2020 Year 08 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016240


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name