UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013950
Receipt number R000016256
Scientific Title Contribution of Mg supplementation and hight volume hydration to the renal toxicity in patients with lung cancer treated by cisplatin: a historical prospective cohort study.
Date of disclosure of the study information 2014/05/13
Last modified on 2014/05/13 21:30:20

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Basic information

Public title

Contribution of Mg supplementation and hight volume hydration to the renal toxicity in patients with lung cancer treated by cisplatin: a historical prospective cohort study.

Acronym

An examination of reducing the renal toxicity caused by cisplatin.

Scientific Title

Contribution of Mg supplementation and hight volume hydration to the renal toxicity in patients with lung cancer treated by cisplatin: a historical prospective cohort study.

Scientific Title:Acronym

An examination of reducing the renal toxicity caused by cisplatin.

Region

Japan


Condition

Condition

lung cancer patients treated with cisplatin

Classification by specialty

Pneumology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Objective is the contribution of Mg infusion and high volume hydration to reducing the renal toxicity.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

delta creatinine, delta creatinine clearance

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with malignant chest tumors who were receiving their first cycle of cisplatin-based chemotherapy at the Osaka City University Hospital between December 2011 and October 2013.

Key exclusion criteria

We excluded four patients whose complications or medical histories may have affected their renal function.

Target sample size

85


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tatsuo Kimura

Organization

Graduate school of Medicine, Osaka City University

Division name

Department of Respiratory Medicine

Zip code


Address

1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan

TEL

81-6-6645-3916

Email

kimutats@med.osaka-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tatsuo Kimura

Organization

Graduate school of Medicine, Osaka City University

Division name

Department of Respiratory Medicine

Zip code


Address

1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan

TEL

81-6-6645-3916

Homepage URL


Email

kimutats@med.osaka-cu.ac.jp


Sponsor or person

Institute

Department of Respiratory Medicine, Graduate school of Medicine, Osaka City University

Institute

Department

Personal name



Funding Source

Organization

Department of Respiratory Medicine, Graduate school of Medicine, Osaka City University

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


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

2014 Year 05 Month 13 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

Completed

Date of protocol fixation

2013 Year 10 Month 31 Day

Date of IRB


Anticipated trial start date

2013 Year 10 Month 31 Day

Last follow-up date

2013 Year 10 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

until December 2012, we performed conventional high-volume hydration without Mg infusion for cases undergoing cisplatin-based chemotherapy (high-volume Mg-). We initiated the administration of Mg sulfate during the pre-hydration stage in December 2012 (high-volume Mg+). Subsequently, the new low-volume hydration with Mg infusion regimen was initiated in July 2013 (low-volume Mg+).


Management information

Registered date

2014 Year 05 Month 13 Day

Last modified on

2014 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=R000016256


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name