UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000028294
Receipt number R000032290
Scientific Title A study on effectiveness of local anesthetic injected by the pre-administration method in tooth extracted patients with essential hypertension
Date of disclosure of the study information 2017/07/20
Last modified on 2017/07/20 08:26:21

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Basic information

Public title

A study on effectiveness of local anesthetic injected by the pre-administration method in tooth extracted patients with essential hypertension

Acronym

A study on local anesthetic injected by the pre-administration method for patients with essential hypertension

Scientific Title

A study on effectiveness of local anesthetic injected by the pre-administration method in tooth extracted patients with essential hypertension

Scientific Title:Acronym

A study on local anesthetic injected by the pre-administration method for patients with essential hypertension

Region

Japan


Condition

Condition

Periodontitis
Essential hypertension

Classification by specialty

Cardiology Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We investigate the effect of divided administration of local anesthesia on the circulatory dynamics of essential hypertension patients at tooth extraction and examine its effectiveness.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

systolic blood pressure 1, 2, 3, 4, 5, 10 minutes after local anesthetic administration

Key secondary outcomes

diastolic blood pressure
pulse rate
rate pressure product


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

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

Maneuver

Interventions/Control_1

1 group: 2% lidocaine with 1/80,000 adrenaline 2.3 ml administration

Interventions/Control_2

2 group: 2% lidocaine with 1/80,000 adrenaline 0.5 ml pre-administration, 1.8 ml administration after 5 minutes

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

Extraction is planned and adult patients with essential hypertension being treated

Key exclusion criteria

Patient taking medication contraindicated with adrenaline

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tohru Akashiba

Organization

The Nippon Dental University Niigata Hospital

Division name

Oral and Maxillofacial Surgery

Zip code


Address

1-8 Hamaura-cho, Chuo-ku Niigata , 951-8151, Japan

TEL

025-267-1500

Email

aka@ngt.ndu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tohru Akashiba

Organization

The Nippon Dental University Niigata Hospital

Division name

Oral and Maxillofacial Surgery

Zip code


Address

1-8 Hamaura-cho, Chuo-ku Niigata , 951-8151, Japan

TEL

025-267-1500

Homepage URL


Email

aka@ngt.ndu.ac.jp


Sponsor or person

Institute

The Nippon Dental University Niigata Hospital

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



Other administrative information

Date of disclosure of the study information

2017 Year 07 Month 20 Day


Related information

URL releasing protocol


Publication of results

Partially published


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

Preinitiation

Date of protocol fixation

2017 Year 07 Month 20 Day

Date of IRB


Anticipated trial start date

2017 Year 07 Month 24 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

2017 Year 07 Month 20 Day

Last modified on

2017 Year 07 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032290


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name