UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000007245
Receipt number R000008495
Scientific Title Optimal reversal dose of Sugammadex in a short post-operative period in adult patients
Date of disclosure of the study information 2012/02/15
Last modified on 2012/08/08 20:53:39

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Optimal reversal dose of Sugammadex in a short post-operative period in adult patients

Acronym

Optimal dose of Sugammadex after rocuronium administration

Scientific Title

Optimal reversal dose of Sugammadex in a short post-operative period in adult patients

Scientific Title:Acronym

Optimal dose of Sugammadex after rocuronium administration

Region

Japan


Condition

Condition

the patients scheduled for elective surgery requiring general anesthesia

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Optimal reversal dose of rocuronium block with Sugammadex

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Evaluation of neuromuscular responses with a peripheral neurostimulator

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Single blind -participants are 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

the group of rising T1 height over 10% after additional dosage of suggamadex

Interventions/Control_2

the group of rising T1 height not over 10% after additional dosage of suggamadex

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

18 years-old <=

Age-upper limit

85 years-old >

Gender

Male and Female

Key inclusion criteria

the patients scheduled for elective surgery requiring general anesthesia.

the patients were ASA physical status 1-2.

Key exclusion criteria

the patients were ASA physical status 3-4.

the diabetic patients.

the patients who heve neurodegenerating disease.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shigeaki Otomo

Organization

Asahikawa Medical University

Division name

Anesthesiology And Critical Care Medicine

Zip code


Address

2-1-1-1 Midorigaoka Higashi Asahikawa Hokkaido Japan

TEL

+81-166-68-2583

Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Asahikawa Medical University

Division name

Anesthesiology And Critical Care Medicine

Zip code


Address


TEL

0166-68-2583

Homepage URL


Email



Sponsor or person

Institute

Department of Anesthesiology and Critical Care Medicine,
Asahikawa Medical University

Institute

Department

Personal name



Funding Source

Organization

None

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

旭川医科大学病院(北海道)


Other administrative information

Date of disclosure of the study information

2012 Year 02 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

Completed

Date of protocol fixation

2012 Year 01 Month 27 Day

Date of IRB


Anticipated trial start date

2012 Year 03 Month 01 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

2012 Year 02 Month 08 Day

Last modified on

2012 Year 08 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008495


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name