UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000032596
Receipt number R000037166
Scientific Title Changes in respiratory status caused by nitrous oxide during general anesthesia
Date of disclosure of the study information 2018/05/15
Last modified on 2019/02/05 07:47:32

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Basic information

Public title

Changes in respiratory status caused by nitrous oxide during general anesthesia

Acronym

Changes in respiratory status caused by nitrous oxide during general anesthesia

Scientific Title

Changes in respiratory status caused by nitrous oxide during general anesthesia

Scientific Title:Acronym

Changes in respiratory status caused by nitrous oxide during general anesthesia

Region

Japan


Condition

Condition

Patients who undergo general anesthesia

Classification by specialty

Child

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effect of nitrous oxide on tidal volume and partial pressure of end tidal and arterial carbon dioxide

Basic objectives2

Pharmacodynamics

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Changes in the tidal volume and partial pressure of end tidal and arterial carbon dioxide from the control

Key secondary outcomes

1. Changes in the lung compliance
2. Changes in the airway resistance
3. Body temperature
4. Cahanges in the end tidal sevoflurane concentration


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

We sustain anesthesia with concentration of 1MAC sevoflurane. Ventilator setting is pressure control ventilation with PEEP 5 cmH2O, tidal volume about 8 mL/kg, and adequate respiratory rate which maintains partial pressure of end tidal carbon dioxide 35-40 mmHg. Initial fresh gas flow is 4 L/min at an FIO2 0.25 in air. We measure respiratory status (tidal volume and partial pressure of end tidal and arterial carbon dioxide) as the control-1.
After measurement of the control-1, we alter FIO2 value to 0.3 in air and measure respiratory status as the air group 10 minutes or more after alteration.

Interventions/Control_2

After measurement of the air group, we alter FIO2 value to 0.25 again and measure respiratory status as the control-2 10 minutes or more after alteration.
After measurement of the control-2, we alter FIO2 value to 0.3 in nitrous oxide and measure respiratory status as the nitrous oxide group 10 minutes or more after alteration.

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

1 years-old <=

Age-upper limit

12 years-old >

Gender

Male and Female

Key inclusion criteria

1. Patients who undergo surgery at our hospital with general anesthesia using inhalational anesthetic
2. Supine position,
3. ASA-PS1,2
4. Intubated cuffed tracheal tube
5. Monitored with arterial line

Key exclusion criteria

1. Patient who have cardiac, respiratory, or neuromuscular disease
2. Patient who have upper respiratory infection
3. Extraordinary operation

Target sample size

5


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tomonari Shinozaki

Organization

Miyagi children's hospital

Division name

department of anesthesiology

Zip code


Address

4-3-17, Ochiai, Aoba-ku Sendai-shi, Miyagi, Japan

TEL

022-391-5111

Email

tmn316@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tomonari Shinozaki

Organization

Miyagi children's hospital

Division name

department of anesthesiology

Zip code


Address

4-3-17, Ochiai, Aoba-ku Sendai-shi, Miyagi, Japan

TEL

022-391-5111

Homepage URL


Email

tmn316@yahoo.co.jp


Sponsor or person

Institute

Miyagi children's hospital

Institute

Department

Personal name



Funding Source

Organization

none

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

2018 Year 05 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

Open public recruiting

Date of protocol fixation

2018 Year 05 Month 14 Day

Date of IRB


Anticipated trial start date

2018 Year 05 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

2018 Year 05 Month 15 Day

Last modified on

2019 Year 02 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000037166


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name