UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025927
Receipt number R000029802
Scientific Title Patient's acceptance of non-stick method for anesthesia of trannasal endoscopy
Date of disclosure of the study information 2017/01/31
Last modified on 2020/06/02 13:14:14

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Basic information

Public title

Patient's acceptance of non-stick method for anesthesia of trannasal endoscopy

Acronym

Patient's acceptance of non-stick method for anesthesia of trannasal endoscopy

Scientific Title

Patient's acceptance of non-stick method for anesthesia of trannasal endoscopy

Scientific Title:Acronym

Patient's acceptance of non-stick method for anesthesia of trannasal endoscopy

Region

Japan


Condition

Condition

upper gastrointestinal disease

Classification by specialty

Gastroenterology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the patient's acceptance of non-stick method for nasal endoscopy

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

VSA of nasal pain during endoscopic examination

Key secondary outcomes

VSA of nasal patient's acceptance during endoscopic examination, the success rate of endoscopic insertion and nasal hemorrhage


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Maneuver

Interventions/Control_1

Transnasal endoscopic examination was performed using non-stick method for anesthesia

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

20 years-old <=

Age-upper limit

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Cases evaluated by unsadated upper gastrointestinal endoscopy

Key exclusion criteria

Cases with severe complications are excluded

Target sample size

800


Research contact person

Name of lead principal investigator

1st name Masashi
Middle name
Last name Hattori

Organization

Medical corporation Yamashita Hospital

Division name

Gastroenterology

Zip code

4918531

Address

1-3-5, Nakamachi, Ichinomiya

TEL

0586-45-4511

Email

m.hattori@yamashita.or.jp


Public contact

Name of contact person

1st name Ippei
Middle name
Last name Matsuzaki

Organization

Medical corporation Yamashita Hospital

Division name

Gastroenterology

Zip code

4918531

Address

1-3-5, Nakamachi, Ichinomiya

TEL

0586-45-4511

Homepage URL


Email

imatsu@med.nagoya-u.ac.jp


Sponsor or person

Institute

Medical corporation Yamashita Hospital

Institute

Department

Personal name



Funding Source

Organization

Medical corporation Yamashita 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

Medical corporation Yamashita Hospital

Address

1-3-5, Nakamachi, Ichinomiya

Tel

0586-45-4511

Email

y.okudaira@yamashita.or.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

2017 Year 01 Month 31 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

2017 Year 01 Month 31 Day

Date of IRB

2017 Year 01 Month 26 Day

Anticipated trial start date

2017 Year 01 Month 31 Day

Last follow-up date

2018 Year 01 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

2017 Year 01 Month 31 Day

Last modified on

2020 Year 06 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029802


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name