UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043925
Receipt number R000042200
Scientific Title Safety Assessment of Ultra-low-flow and Low-flow Sevoflurane Anesthesia Using Carbon Dioxide Absorbent YABASHI LIME-f
Date of disclosure of the study information 2021/04/14
Last modified on 2021/10/14 10:42:06

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Basic information

Public title

Safety Assessment of Ultra-low-flow and Low-flow Sevoflurane Anesthesia Using Carbon Dioxide Absorbent YABASHI LIME-f

Acronym

SAULSAY

Scientific Title

Safety Assessment of Ultra-low-flow and Low-flow Sevoflurane Anesthesia Using Carbon Dioxide Absorbent YABASHI LIME-f

Scientific Title:Acronym

SAULSAY

Region

Japan


Condition

Condition

Colon cancer, Benign colorectal disease

Classification by specialty

Surgery in general Gastrointestinal surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

In this study, we use Yabashilime-f and perform respiratory control under sevoflurane anesthesia with a fresh gas flow rate of 0.5 L / min (very low flow rate), 1 L / min (low flow rate), or 2 L / min of normal flow rate. In colorectal disease surgery, we will evaluate the concentration of Compound A in the anesthesia circuit over time and the presence or absence of postoperative acute kidney injury onset in patients. This will examine whether sevoflurane very low flow anesthesia and low flow anesthesia surgery can be performed without causing renal dysfunction.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Measurement of Compound A concentration in anesthesia circuit over time

Key secondary outcomes

Whether the patient has postoperative acute kidney disease


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Dose comparison

Stratification

NO

Dynamic allocation

YES

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

No need to know


Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

fresh gas frow rate 0.5 L/h

Interventions/Control_2

fresh gas frow rate 1 L/h

Interventions/Control_3

fresh gas frow rate 2 L/h

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

Scheduled colon cancer resection ( over 6 hours anesthesia )

Key exclusion criteria

Renal function is normal (eGFR 90 or more) and liver function is normal (total bilirubin is 1.5 times or less of the upper limit of the medical institution's standard value and AST and ALT are 2.5 times or less of the upper limit of the medical institution's standard value)

Target sample size

18


Research contact person

Name of lead principal investigator

1st name Kimitoshi
Middle name
Last name Nishiwaki

Organization

Nagoya university graduate school of medicine

Division name

Department of anesthesiology

Zip code

466-8550

Address

65 tsurumai showa nagoya

TEL

052-744-2340

Email

nishi@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Takahiro
Middle name
Last name Ando

Organization

Nagoya university hospital

Division name

Department of surgery section

Zip code

466-8550

Address

65 tsurumai showa nagoya

TEL

052-744-2340

Homepage URL


Email

bakagarasu7@gmail.com


Sponsor or person

Institute

Nagoya university graduate school of medicine

Institute

Department

Personal name



Funding Source

Organization

Nagoya university graduate school of medicine

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 university graduate school of medicine

Address

65 tsurumai showa nagoya

Tel

052-744-2973

Email

ethics@med.nagoya-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

2021 Year 04 Month 14 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

2019 Year 08 Month 15 Day

Date of IRB

2019 Year 08 Month 15 Day

Anticipated trial start date

2019 Year 08 Month 15 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 04 Month 14 Day

Last modified on

2021 Year 10 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042200


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name