UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010705
Receipt number R000012513
Scientific Title Safety and effectiveness of robotic assisted laparoscopic pyeloplasty using da Vinci S surgical system
Date of disclosure of the study information 2013/05/15
Last modified on 2013/05/13 19:52:11

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Basic information

Public title

Safety and effectiveness of robotic assisted laparoscopic pyeloplasty using da Vinci S surgical system

Acronym

Safety and effectiveness of robotic assisted laparoscopic pyeloplasty

Scientific Title

Safety and effectiveness of robotic assisted laparoscopic pyeloplasty using da Vinci S surgical system

Scientific Title:Acronym

Safety and effectiveness of robotic assisted laparoscopic pyeloplasty

Region

Japan


Condition

Condition

Ureteropelvic Junction Obstruction

Classification by specialty

Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effectiveness and feasibility of robotic-assisted laparoscopic radical cystectomy in patients with invasive bladder cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Improvement of the hydronephrosis

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Robotic-assisted laparoscopic pyeloplasty

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

Patients with ureteropelvic Junction Obstruction.
No evidence of distant metastasis.
Age 20 years old or more, and less than 80 years old.
Patients who wish to come into compliance with protocol.
Each patient voluntarily gave written informed consent before treatment.

Key exclusion criteria

Patients who is or may be pregnant.
Patients who is breast feeding at the time of treatment.
Patients who are not suitable for laparoscopic surgery.
Patients who are not considered for being eligible to this trial by investigator.

Target sample size

5


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kanayama Hiro-omi

Organization

Tokushima university

Division name

Department of Urology

Zip code


Address

3-18-15 Kuramoto-cho Tokushima

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Tokushima university

Division name

depatment of urology

Zip code


Address


TEL


Homepage URL


Email



Sponsor or person

Institute

Tokushima university

Institute

Department

Personal name



Funding Source

Organization

Tokushima 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



Other administrative information

Date of disclosure of the study information

2013 Year 05 Month 15 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

Preinitiation

Date of protocol fixation

2013 Year 05 Month 15 Day

Date of IRB


Anticipated trial start date

2013 Year 05 Month 21 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

2013 Year 05 Month 13 Day

Last modified on

2013 Year 05 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012513


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name