UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022459
Receipt number R000025881
Scientific Title Optimum fluid therapy to minimize the postoperative complications of long surgery : randomized controlled trial
Date of disclosure of the study information 2016/07/01
Last modified on 2019/03/29 09:00:30

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Basic information

Public title

Optimum fluid therapy to minimize the postoperative complications of long surgery : randomized controlled trial

Acronym

Study of optimal fluid therapy and lung protection ventilation to minimize the postoperative complications of long surgery

Scientific Title

Optimum fluid therapy to minimize the postoperative complications of long surgery : randomized controlled trial

Scientific Title:Acronym

Study of optimal fluid therapy and lung protection ventilation to minimize the postoperative complications of long surgery

Region

Japan


Condition

Condition

Gastrointestinal Surgery

Classification by specialty

Gastrointestinal surgery Hepato-biliary-pancreatic surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To clarify the optimal combination of ifluid therapy and optimal respiration method of managing long abdominal surgery

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Postoperative hospital stay

Key secondary outcomes

Postoperative complications of up to either early the day of up to hospital discharge after surgery or 28 days


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment

Pseudo-randomization


Intervention

No. of arms

4

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Restrictive transfusion management /
1) with respect to blood pressure lowering at the time of induction of anesthesia, the administration of phenylephrine.
2) intraoperative maintenance infusion dose and 3ml / kg / h.
3) If the stroke volume change of arterial pressure cardiac output sensor (flow tracks) (SVV) becomes 15 or more, VOL (: 6% HES130 / 0.4 / 9) rapidly administering the (5ml / kg) and, if .SVV that SVV is to stop administered in 13 or less is 13 or more, again, rapid administration (5ml / kg) of the VOL.
4) If the amount of urine is less than or equal to 0.5ml / kg / h, to VOL bolus administration (5ml / kg).
5) the time of bleeding, if the Hb is 7 or less, to start the transfusion of packed red blood cells, as long as 7 or more, the amount of bleeding and an equal amount administering the VOL.
6) blood pressure is lowered, if you do not want to recover the baseline value in the above infusion management will review the administration of the vasoconstrictor, if SVI is less than or equal to 35, to consider the DOB administration.

Interventions/Control_2

Non-limiting infusion management /
1) For low blood pressure during anesthesia induction, when administering a crystalloid solution. Responsible anesthesiologist physician determines that it is necessary to vasopressors, administering an appropriate vasopressor.
2) Maintenance infusion is administered at 6ml / kg / h.
3) hemodynamic after crystalloid fluid administration to measure the baseline vital signs in a stable point in time, blood pressure, HR together so as to maintain the baseline value 20%, managed by the amorphous liquid dosage and vasoconstrictor to.
4) If the amount of urine is less than or equal to 1ml / kg / h, the rapid administration of the VOL (5ml / kg).
5) With respect to anesthesia management other than those described above and the judgment of the attending anesthesiologist.

Interventions/Control_3

Lung protection management /
1) pressure-limited ventilation with PEEP (the positive end-expiratory pressure) is set to 5 ~ 10cmH2O, tidal
The amount shall be 5 ~ 7ml / kg.
2) PaO2 / FIO2 (P / F ratio: the arterial pressure oxidation oxygen partial pressure / inhalation phase oxygen partial pressure) lung pressure is when it becomes 80% or less of the case or the expected P / F ratio falls below 400 make up to 1 times / h. Lung pressurizing method is, I: E: the (inspiratory time expiratory time) 0.8 seconds: using a three-breathing 0.5 seconds. (High peep: 45 / low peep: 10)
3) extubation, the pressurized pressure relief tube, when it is not necessary, the endotracheal suction is not performed.

Interventions/Control_4

A non-lung-protective ventilator management / 1) PEEP 5cmH2O, tidal volume and 8 ~ 10ml / kg.
2) pulmonary pressure is not performed.
3) at the time of extubation to pressure the pressure relief tube from the suction in the trachea.

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

1)Undergo elective abdominal surgery of more than 3 hours elective surgery time in our hospital, the patient's plan to use the intraoperative arterial pressure catheter
2)Adult patients test responsible can understand the description of the doctor, can be their own signature
3)The weight of the patient 35Kg during surgery

Key exclusion criteria

1) Patient ASA-PS is 3 or more
2) Patients can not be controlled by drug therapy cardiogenic of arrhythmia is as comorbidities
3) Pregnant patient
4) Patients with unresectable malignant tumors in addition to the surgical site
5) Patients other attending physician and responsible anesthesiology physician, it is determined that it should not participate in the study

Target sample size

260


Research contact person

Name of lead principal investigator

1st name Kohji
Middle name
Last name Uzawa

Organization

Kyorin University Hospital

Division name

Department of Anesthesiology

Zip code

181-0004

Address

6-20-2 Shinkawa Mitaka City Tokyo Japan

TEL

0422-47-5511

Email

kohji.fentanyl@gmail.com


Public contact

Name of contact person

1st name Kohji
Middle name
Last name Uzawa

Organization

Kyorin University Hospital

Division name

Department of Anesthesiology

Zip code

181-0004

Address

6-20-2 Shinkawa Mitaka City Tokyo Japan

TEL

0422-47-5511

Homepage URL


Email

kohji.fentanyl@gmail.com


Sponsor or person

Institute

Kyorin University

Institute

Department

Personal name



Funding Source

Organization

kyorin university

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kyorin University School of Medicine Ethics Committee

Address

6-20-2 Shinkawa Mitaka-shi Tokyo Japan

Tel

0422-47-5511

Email

irb@ks.kyorin-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

杏林大学病院(東京都)


Other administrative information

Date of disclosure of the study information

2016 Year 07 Month 01 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

2016 Year 07 Month 01 Day

Date of IRB

2016 Year 05 Month 02 Day

Anticipated trial start date

2016 Year 07 Month 01 Day

Last follow-up date

2019 Year 03 Month 28 Day

Date of closure to data entry

2019 Year 03 Month 28 Day

Date trial data considered complete

2019 Year 03 Month 28 Day

Date analysis concluded

2019 Year 12 Month 31 Day


Other

Other related information



Management information

Registered date

2016 Year 05 Month 25 Day

Last modified on

2019 Year 03 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025881


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name