UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024561
Receipt number R000028165
Scientific Title Efficacy and safety of sedative agents for endoscopic submucosal dissection of esophageal carcinoma
Date of disclosure of the study information 2016/10/25
Last modified on 2022/05/02 20:22:38

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Basic information

Public title

Efficacy and safety of sedative agents for endoscopic submucosal dissection of esophageal carcinoma

Acronym

Efficacy and safety of sedative agents for endoscopic submucosal dissection of esophageal carcinoma

Scientific Title

Efficacy and safety of sedative agents for endoscopic submucosal dissection of esophageal carcinoma

Scientific Title:Acronym

Efficacy and safety of sedative agents for endoscopic submucosal dissection of esophageal carcinoma

Region

Japan


Condition

Condition

esophageal carcinoma

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To reveal efficacy and safety of propofol and midazolam in ESD for early esophageal cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

treatment performance for endoscopic submucosal dissection using midazolam or propofol

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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


Not applicable

Gender

Male and Female

Key inclusion criteria

The patients who have a superficial esophageal cancer treated by endoscopic resection or esophagectomy

Key exclusion criteria

Patients whom a researcher judged to be inappropriate as a subject.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Yuji
Middle name
Last name Naito

Organization

Kyoto Prefectural University of Medicine

Division name

Department of Molecular Gastroenterology and Hepatology

Zip code

602-8566

Address

465 Kajii-cho, Kamigyo-ku, Kyoto, Japan

TEL

075-251-5519

Email

ynaito@koto.kpu-m.ac.jp


Public contact

Name of contact person

1st name Osamu
Middle name
Last name Dohi

Organization

Kyoto Prefectural University of Medicine

Division name

Department of Molecular Gastroenterology and Hepatology

Zip code

602-8566

Address

465 Kawaramachi Hirokoji Kamigyo-ku, Kyoto

TEL

075-251-5519

Homepage URL


Email

osamu-d@koto.kpu-m.ac.jp


Sponsor or person

Institute

Kyoto Prefectural University of Medicine

Institute

Department

Personal name



Funding Source

Organization

Kyoto Prefectural University of Medicine

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

Kyoto Prefectural University of Medicine

Address

465 Kajiicho Hirokoji Kawaramachi Kamigyo-ku, Kyoto, Japan

Tel

0752515337

Email

rinri@koto.kpu-m.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

2016 Year 10 Month 25 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 06 Month 15 Day

Date of IRB

2017 Year 03 Month 03 Day

Anticipated trial start date

2016 Year 10 Month 25 Day

Last follow-up date

2020 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Clinical information was reviewed retrospectively.


Management information

Registered date

2016 Year 10 Month 25 Day

Last modified on

2022 Year 05 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028165


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name