UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009070
Receipt number R000010488
Scientific Title Phase II study of Neoadjuvant chemotherapy with Gemcitabine and S1 (GS therapy) for resectable pancreatic carcinoma (NAC GS2+2)
Date of disclosure of the study information 2012/10/15
Last modified on 2017/10/03 10:39:19

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Basic information

Public title

Phase II study of Neoadjuvant chemotherapy with Gemcitabine and S1 (GS therapy) for resectable pancreatic carcinoma (NAC GS2+2)

Acronym

Phase II study of Neoadjuvant chemotherapy with Gemcitabine and S1 (GS therapy) for resectable pancreatic carcinoma (NAC GS2+2)

Scientific Title

Phase II study of Neoadjuvant chemotherapy with Gemcitabine and S1 (GS therapy) for resectable pancreatic carcinoma (NAC GS2+2)

Scientific Title:Acronym

Phase II study of Neoadjuvant chemotherapy with Gemcitabine and S1 (GS therapy) for resectable pancreatic carcinoma (NAC GS2+2)

Region

Japan


Condition

Condition

resectable pancreatic cancer

Classification by specialty

Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and feasibilty for gemcitabine and S1 therapy as Neoadjuvant against pancreatic cancer

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase II


Assessment

Primary outcomes

True R0 resection rate; The rate of R0 resection with the normalized post-operative tumor markers

Key secondary outcomes

Adverse effect, pathological effect, recurrence free survival, overall survival, patterns of recurrence, reduction rate and normalization rate for tumor marker


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

Interventions/Control_1

Neoadjuvant chemotherapy with gemcitabine and S1

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) invasive ductal carcinoma of the pancreas
2) no distant metastasis
3) R0/1 resectable
4) all adult who anticipate to undergo pancreatectomy
5) no prior therapy
6) written informed consent

Key exclusion criteria

1) pulmonary fibrosis or interstitial pneumonitis
2) tumor other than ductal carcinoma
3) distant metastasis
4) R2 resection
5) prior anti-cnacer therapy
6) pregnancy
7) under 18 years old

Target sample size

35


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Michiaki Unno

Organization

Tohoku University Graduate School of Medicine

Division name

Gastroenterological Surgery

Zip code


Address

1-1, Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan

TEL

022-717-7205

Email

m_unno@surg1.med.tohoku.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kei Nakagawa

Organization

NEXTSURG

Division name

Coordinating office

Zip code


Address

1-1, Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan

TEL

022-343-9234

Homepage URL

http://nextsurg.kenkyuukai.jp/about/

Email

kein_h11@surg1.med.tohoku.ac.jp


Sponsor or person

Institute

NEXTSURG

Institute

Department

Personal name



Funding Source

Organization

None (Self-funding)

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

2012 Year 10 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

Terminated

Date of protocol fixation

2012 Year 08 Month 24 Day

Date of IRB


Anticipated trial start date

2012 Year 10 Month 15 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

2012 Year 10 Month 09 Day

Last modified on

2017 Year 10 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010488


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name