UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000021068
Receipt number R000024165
Scientific Title New Diagnostic Method of Lymph Nodes metastases and Surgical Margins Using 5-Aminolevulinic Acid in Urothelial Carcinoma and Prostate Cancer.
Date of disclosure of the study information 2016/06/01
Last modified on 2023/03/03 13:53:08

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Basic information

Public title

New Diagnostic Method of Lymph Nodes metastases and Surgical Margins Using 5-Aminolevulinic Acid in Urothelial Carcinoma and Prostate Cancer.

Acronym

Diagnosis of lymph nodes metastases of urological malignancy using 5-ALA

Scientific Title

New Diagnostic Method of Lymph Nodes metastases and Surgical Margins Using 5-Aminolevulinic Acid in Urothelial Carcinoma and Prostate Cancer.

Scientific Title:Acronym

Diagnosis of lymph nodes metastases of urological malignancy using 5-ALA

Region

Japan


Condition

Condition

Urothelial cancer, Prostate cancer

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy of new diagnosis system using 5-ALA for urothelial carcinoma and prostate cancer as pathological diagnosis during surgery

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Efficacy

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

Diagnosis

Type of intervention

Medicine Device,equipment

Interventions/Control_1

Single oral dose of 5-ALA before surgery

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Prostate or urothelial cancer who undergo prostatectomy, cystectomy or nephroureterectomy

PS 0-1

given written informed consent

Key exclusion criteria

Porphyria
Hypersensitivity of 5-ALA
pregnant or possibly pregnant women
severe cardiac, pulmonary, renal, hepatic, or hematopoietic impairment or uncontrolled diabetes mellitus

Target sample size

250


Research contact person

Name of lead principal investigator

1st name Osamu
Middle name
Last name Ukimura

Organization

Kyoto Prefectural University of Medicine

Division name

Department of Urology

Zip code

6028566

Address

465 kajiicho, Kamigyoku, Kyoto

TEL

075-251-5595

Email

ukimura@koto.kpu-m.ac.jp


Public contact

Name of contact person

1st name Yoshio
Middle name
Last name Naya

Organization

Kyoto Prefectural University of Medicine

Division name

Department of Urology

Zip code

6028566

Address

465kajiicho, Kamigyoku, Kyoto

TEL

075-251-5595

Homepage URL


Email

ynaya@koto.kpu-m.ac.jp


Sponsor or person

Institute

Kyoto Prefectural University of Medicine

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

USHIO INC.

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kyoto Prefectural University of Medicine, Clinical Reserach Review Board

Address

465 kajii-cho, Kawaramachi-Hirokoji, kamigyo-ku, Kyoto, japan

Tel

075-251-5337

Email

rinri@koto.kpu-m.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

2016 Year 06 Month 01 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

Terminated

Date of protocol fixation

2016 Year 02 Month 17 Day

Date of IRB

2016 Year 02 Month 17 Day

Anticipated trial start date

2016 Year 06 Month 01 Day

Last follow-up date

2022 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 02 Month 17 Day

Last modified on

2023 Year 03 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000024165


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name