UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029734
Receipt number R000033970
Scientific Title Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2 against local failure after chemoradiotherapy or radiotherapy for esophageal cancer
Date of disclosure of the study information 2017/10/27
Last modified on 2019/10/30 18:46:50

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Basic information

Public title

Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2 against local failure after chemoradiotherapy or radiotherapy for esophageal cancer

Acronym

Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2

Scientific Title

Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2 against local failure after chemoradiotherapy or radiotherapy for esophageal cancer

Scientific Title:Acronym

Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2

Region

Japan


Condition

Condition

esophageal cancer

Classification by specialty

Medicine in general Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Photodymanic diagnosis against esophageal cancer by using Talaporfin and Sie-P2.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Phase I


Assessment

Primary outcomes

Safety and efficacy of PDD

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

PDD

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

1.The patient of recurrent esopphageal cacner after CRT who will be trated by Photodynamic therapy(PDT) with Talaporfin. Local failure after CRT or RT:more than 50Gy
2.histologically proven local failure
3.either not candidates for salvage surgery or having a physical status that would make the surgery intolerable
4.lesions limited to within the muscularis propria
5.age more than 20 years old
6.the patient who has no disturbance in liver and kidney.
7.provision of written informed consent

Key exclusion criteria

1. the patinet who can not be inserted endoscope
2. with malignant hypertension, conjestive heart failure, liver dysfunction, myocardil infarction within 3 months, endostage of liver cirrhosis, poor controled DM, severe lung fibrosis, active pneumonitis
3. with active infection
4. inability to comply the sun shade restrictions
5. porphyria
6. severe psychosomatic disturbance
7. allergy against Talaporfin
8. for women, pregnancy or lactation,
or unwillingness to use contraception
9. T3 or T4
10. larger than 3cm in diameter
11. half the circumference of the lumen or less
12. invasion to the cervical esophagus
13. patients who judged by the investigator that enrollment was inappropriate

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Hiromi
Middle name
Last name Kataoka

Organization

Nagoya City University Hospital

Division name

Division of Endoscopy

Zip code

467-8601

Address

1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya

TEL

052-851-5511

Email

hkataoka@med.nagoya-cu.ac.jp


Public contact

Name of contact person

1st name Hiromi
Middle name
Last name Kataoka

Organization

Division of Gastroenterology

Division name

Division of Gastroenterology

Zip code

467-8601

Address

1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya

TEL

052-851-5511

Homepage URL


Email

hkataoka@med.nagoya-cu.ac.jp


Sponsor or person

Institute

Nagoya City University Hospital

Institute

Department

Personal name



Funding Source

Organization

nothing

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nagoya City University

Address

1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya

Tel

052-851-5511

Email

hkataoka@med.nagoya-cu.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

名古屋市立大学病院(愛知県)


Other administrative information

Date of disclosure of the study information

2017 Year 10 Month 27 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

2

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

2017 Year 10 Month 24 Day

Date of IRB

2018 Year 02 Month 07 Day

Anticipated trial start date

2018 Year 04 Month 07 Day

Last follow-up date

2018 Year 12 Month 04 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 10 Month 27 Day

Last modified on

2019 Year 10 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033970


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name