UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013785
Receipt number R000015290
Scientific Title Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system
Date of disclosure of the study information 2014/04/23
Last modified on 2016/05/31 20:34:42

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Basic information

Public title

Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system

Acronym

Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system

Scientific Title

Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system

Scientific Title:Acronym

Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system

Region

Japan


Condition

Condition

renal tumor

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Clinical trial on the efficacy and safety of robot assisted laparoscopic partial nephrectomy using Davinci surgical system

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Efficacy and safety of robot assisted laparoscopic partial nephrectomy
(surgical margine negative,WIT<25min,no blood transfusion,no complication)

Key secondary outcomes

operative time, complication, pathology, prognosis


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

patient of renal cellcarcinoma

Interventions/Control_2


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

80 years-old >

Gender

Male and Female

Key inclusion criteria

clinical stage T1aN0M0

Key exclusion criteria

performance status 2
ASA 4

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tadashi Matsuda

Organization

Kansai medical university Hirakata hospital

Division name

urology

Zip code


Address

2-3-1 hirakata osaka

TEL

072-804-0101

Email

matsudat@takii.kmu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Motohiko Sugi

Organization

Kansai medical university Hirakata hospital

Division name

urology

Zip code


Address

2-3-1 hirakata osaka

TEL

072-804-0101

Homepage URL


Email

sugim@takii.kmu.ac.jp


Sponsor or person

Institute

the department of urology, kansai medical university

Institute

Department

Personal name



Funding Source

Organization

the department of urology, kansai medical university

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


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

関西医科大学 枚方病院


Other administrative information

Date of disclosure of the study information

2014 Year 04 Month 23 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

Completed

Date of protocol fixation

2014 Year 04 Month 23 Day

Date of IRB


Anticipated trial start date

2014 Year 05 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 04 Month 22 Day

Last modified on

2016 Year 05 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015290


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name