UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000032360
Receipt number R000028907
Scientific Title Influence of supporting method of tracheal tube during general anesthesia on postoperative sore throat
Date of disclosure of the study information 2018/04/24
Last modified on 2023/11/08 16:38:17

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Basic information

Public title

Influence of supporting method of tracheal tube during general anesthesia on postoperative sore throat

Acronym

Influence of supporting method of tracheal tube during general anesthesia on postoperative sore throat

Scientific Title

Influence of supporting method of tracheal tube during general anesthesia on postoperative sore throat

Scientific Title:Acronym

Influence of supporting method of tracheal tube during general anesthesia on postoperative sore throat

Region

Japan


Condition

Condition

Patients under general anesthesia

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare and examine whether the occurrence frequency of postoperative sore throat pain differs depending on the support method of two tracheal tubes for patients who underwent general anesthesia requiring tracheal intubation at Tsukuba University Hospital. It is a comparison of the tracheal tube support method that is usually done clinically and normally.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

On the day of surgery (2 hours after surgery): Yahara surveyed the presence or absence of sore throat pain and VAS and sore throat score after surgery
Next day after surgery (24 hours after surgery) APS examines the presence or absence of postoperative sore throat and VAS and sore throat score
VAS (0: no postoperative sore throat or hoarseness, 100: maximum imaginable postoperative sore throat or hoarseness)
The frequency and severity of postoperative sore throat pain between the two groups are compared using Chi-square test and Mann-Whitney test.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Cluster

Blinding

Double blind -all involved are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

Natural group: Connect the coiled tube using Godzilla while maintaining the natural shape of the tracheal tube.

Interventions/Control_2

Curved group: Connected to breathing circuit by towing in the plane direction to add curvature of product and curvature to right 90 degrees direction. The force applying curvature is the upper limit force that the lumen of the tracheal tube does not deform from the normal circle.

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

85 years-old >=

Gender

Male and Female

Key inclusion criteria

The subject is scheduled surgical patient for adult male and female (20 years old to 85 years old).

Key exclusion criteria

Smoker, more than 180 minutes, indwelling nasogastric tube, insertion of pharyngeal probes, tracheal aspiration, cases where intubation failed in one trial, patients requiring head and neck surgery, sputum

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Musashi Yahagi

Organization

University of Tsukuba Hospital

Division name

Department of Anesthesia

Zip code


Address

Osaka Suita Aoyamadai 3-32-7

TEL

08033348696

Email

musasum0710@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Musashi Yahagi

Organization

University of Tsukuba Hospital

Division name

Department of Anesthesia

Zip code


Address

Ibaraki Tsukuba Tennodai 2-1-1

TEL

029-853-3900

Homepage URL


Email

musasum0710@yahoo.co.jp


Sponsor or person

Institute

University of Tsukuba Hospital

Institute

Department

Personal name



Funding Source

Organization

University of Tsukuba Hospital

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


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 04 Month 24 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 01 Month 01 Day

Date of IRB

2016 Year 07 Month 01 Day

Anticipated trial start date

2016 Year 08 Month 01 Day

Last follow-up date

2023 Year 11 Month 08 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 04 Month 24 Day

Last modified on

2023 Year 11 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028907


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name