UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037660
Receipt number R000042946
Scientific Title Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline
Date of disclosure of the study information 2019/09/01
Last modified on 2019/08/10 16:59:58

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Basic information

Public title

Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline

Acronym

Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline

Scientific Title

Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline

Scientific Title:Acronym

Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline

Region

Japan


Condition

Condition

none

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Analysis of hemodynamic alteration triggered by infiltration anesthesia using lidocaine with adrenaline

Basic objectives2

PK,PD

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

SVR before and after using local anesthetic for dental use

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

15 years-old <=

Age-upper limit

99 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients planning dental treatment in the operating room of Showa University Dental Hospital

Key exclusion criteria

1) Patients with contraindications to anesthetics and local anesthetics used during surgery
2) Patients suffering from severe liver / kidney disorder or heart disease that may affect the operation
3) Patients judged to be ineligible based on the judgment of the doctor in charge
4) Patients who have not given consent for participation in this study

Target sample size

30


Research contact person

Name of lead principal investigator

1st name kanamrua
Middle name
Last name masako

Organization

showa university

Division name

Department of Perioperative Medicine,Division of Anesthesiology

Zip code

145-8515

Address

2-1-1 Kitasenzuka, Ota-ku, Tokyo

TEL

03-3787-1151

Email

ka76ra@dent.showa-u.ac.jp


Public contact

Name of contact person

1st name kanamura
Middle name
Last name masako

Organization

showa university

Division name

Department of Perioperative Medicine,Division of Anesthesiology

Zip code

145-8515

Address

2-1-1 Kitasenzuka, Ota-ku, Tokyo

TEL

03-3787-1151

Homepage URL


Email

ka76ra@dent.showa-u.ac.jp


Sponsor or person

Institute

showa university

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

showa university

Address

2-1-1 Kitasenzuka, Ota-ku, Tokyo

Tel

03-3787-1151

Email

ka76ra@dent.showa-u.ac.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

DH-2019-007

Org. issuing International ID_1

showa university

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2019 Year 09 Month 01 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

26

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

2019 Year 05 Month 27 Day

Date of IRB

2019 Year 05 Month 27 Day

Anticipated trial start date

2019 Year 05 Month 27 Day

Last follow-up date

2019 Year 05 Month 27 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

none


Management information

Registered date

2019 Year 08 Month 10 Day

Last modified on

2019 Year 08 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042946


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name