UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022303
Receipt number R000025696
Scientific Title A Phase II trial of neoadjuvant therapy with GEM/IMRT for potentially resectable pancreatic cancer
Date of disclosure of the study information 2016/06/07
Last modified on 2016/05/13 15:22:51

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Basic information

Public title

A Phase II trial of neoadjuvant therapy with GEM/IMRT for potentially resectable pancreatic cancer

Acronym

Neoadjuvant chemoradiation therapy for potentially resectable pancreatic cancer

Scientific Title

A Phase II trial of neoadjuvant therapy with GEM/IMRT for potentially resectable pancreatic cancer

Scientific Title:Acronym

Neoadjuvant chemoradiation therapy for potentially resectable pancreatic cancer

Region

Japan


Condition

Condition

potentially resectable pancreatic cancer

Classification by specialty

Hepato-biliary-pancreatic medicine Hepato-biliary-pancreatic surgery Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and safety of neoadjuvant chemoradiation therapy using Gemcitabine combined with IMRT for potentially resectable pancreatic cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Phase II


Assessment

Primary outcomes

overall survival

Key secondary outcomes

disease-free survival, pathological responce rate, incident of adverse event, mortality


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

Medicine Maneuver

Interventions/Control_1

To investigate the overall survival rate following chemoradiation using Gemcitabine combined with IMRT for potentially resectable pancreatic cancer

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

1.Patients with Histo-cytologically confirmed pancreatic cancer
2.Patients with radiologically defined patentially borderline resectable pancreatic cancer
3.Patients with Performance status of 0/1
4.Patients who have not undergone chemo and/or radiotherapyPatients with no metastatic disease confirmed by staging laparoscopy
5.Patiants who can oral intake
6.Patients with normal ECG findings
7.Patients with sustained organ function
8.Patients who received informed consent

Key exclusion criteria

1) Patients with lung fibrosis or interstitional pneumonia
2) Patients who can not underwent radiation therapy because of past radiation therapy
3) Severe co-morbid diseases
4) Intractable pleural and pericardical effusion, or ascites
5) Patients with other active cancers
6)Pregnancy or insufficient contraception
7) severe mental illness
8) Patients seems inadequate for this study by investigator(s)

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shinji Uemoto

Organization

Graduate School of Medicine and Faculty of Medicine, Kyoto University

Division name

Hepato-pancreato-biliary Surgery and Transplantation

Zip code


Address

54 Kawaharacho, Shogoin, Sakyo-ku Kyoto,

TEL

075-751-3242

Email

tmasui@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Toshihiko Masui

Organization

Graduate School of Medicine and Faculty of Medicine KyotoUniversity

Division name

Hepato-pancreato-biliary Surgery and Transplantation

Zip code


Address

54 Kawaharacho, Shogoin, Sakyo-ku Kyoto,

TEL

075-751-3242

Homepage URL


Email

tmasui@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Kyoto University

Institute

Department

Personal name



Funding Source

Organization

Hepato-pamcreato-biliary Surgery and Transplantation,
Graduate School of Medicine and Faculty of Medicine, Kyoto 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

京都大学医学部附属病院(京都府)


Other administrative information

Date of disclosure of the study information

2016 Year 06 Month 07 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

Open public recruiting

Date of protocol fixation

2016 Year 05 Month 07 Day

Date of IRB


Anticipated trial start date

2016 Year 06 Month 13 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

2016 Year 05 Month 13 Day

Last modified on

2016 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=R000025696


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name