UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016877
Receipt number R000019595
Scientific Title A phase I/II trial of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function
Date of disclosure of the study information 2015/03/30
Last modified on 2021/03/31 22:10:33

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Basic information

Public title

A phase I/II trial of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function

Acronym

A phase I/II trial of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function

Scientific Title

A phase I/II trial of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function

Scientific Title:Acronym

A phase I/II trial of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function

Region

Japan


Condition

Condition

Patients with resectable pancreatic cancer and impaired renal function

Classification by specialty

Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate efficacy and safety of preoperative chemoradiotherapy with gemcitabine in patients with pancreatic cancer and impaired renal function

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Phase I: Safety
Phase II: Pathological response

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

Medicine

Interventions/Control_1

Preoperative chemoradiotherapy with gemcitabine

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) Histologically proven pancreatic adenocarcinoma
(2) Age between 20 and 80 years
(3) ECOG performance status of 0 or 1
(4) Creatinine clearance <60 ml/min (excluding dialysis patients)
(5) Surgically resectable
(6) Life Expectancy must be >=6 months
(7) Adequate hematologic, hepatic and respiratory function
(8) Interval of at least 4 weeks between prior treatment and start of present study
(9) Written informed consent

Key exclusion criteria

(1) Unresectable pancreatic cancer
(2) Dialysis patients
(3)Presence or past history of interstitial pneumonia or pulmonary fibrosis or possible
(4) Active infections (excluding viral hepatitis)
(5) Severe cardiac disorder, renal disorder, liver disorder, ulcer with bleeding, intestinal tract paralysis, uncontrollable diabetes mellitus
(6) Presence of pleural effusion or ascites requiring drainage
(7) Presence of metastasis in central nervous system
(8) Active double cancer except carcinoma in situ or intramucosal cancer (synchronous double cancer or asynchronous double cancer with disease-free duration to be within 3 years)
(9) Pregnant females or nursing mothers who can not stop lactation. Patients or partners, who don't attempt to doing contraception during the study period.
(10) Severe mental disorder
(11) Severe drug hypersensitivity
(12) As determined by the principal investigator or the sub-investigator the subject is not adequate to participate in the trial.

Target sample size

26


Research contact person

Name of lead principal investigator

1st name Hidetoshi
Middle name
Last name Eguchi

Organization

Osaka University

Division name

Gastroenterological Surgery

Zip code

5650871

Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3251

Email

heguchi@gesurg.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name Hidetoshi
Middle name
Last name Eguchi

Organization

Osaka University

Division name

Gastroenterological Surgery

Zip code

5650871

Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3251

Homepage URL


Email

heguchi@gesurg.med.osaka-u.ac.jp


Sponsor or person

Institute

Clinical Study Group of Osaka University

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

Clinical Study Group of Osaka University

Address

2-2 Yamadaoka, Suita, Osaka, Japan

Tel

06-6879-3251

Email

heguchi@gesurg.med.osaka-u.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

2015 Year 03 Month 30 Day


Related information

URL releasing protocol

https://link.springer.com/article/10.1007/s00280-019-04005-y

Publication of results

Published


Result

URL related to results and publications

https://link.springer.com/article/10.1007/s00280-019-04005-y

Number of participants that the trial has enrolled

8

Results

Refer to paper

Results date posted

2021 Year 03 Month 31 Day

Results Delayed


Results Delay Reason

Refer to paper

Date of the first journal publication of results


Baseline Characteristics

Refer to paper

Participant flow

Refer to paper

Adverse events

Refer to paper

Outcome measures

Refer to paper

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2015 Year 03 Month 11 Day

Date of IRB

2015 Year 03 Month 11 Day

Anticipated trial start date

2015 Year 03 Month 30 Day

Last follow-up date

2017 Year 03 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 03 Month 23 Day

Last modified on

2021 Year 03 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019595


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name