UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051684
Receipt number R000058981
Scientific Title taoc and vaping
Date of disclosure of the study information 2023/07/21
Last modified on 2023/07/21 23:17:13

* 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

taoc and vaping

Acronym

taoc and vaping

Scientific Title

taoc and vaping

Scientific Title:Acronym

taoc and vaping

Region

Asia(except Japan)


Condition

Condition

The lack of clarity regarding the effect of switching to vaping from tobacco cigarettes on gingival health

Classification by specialty

Dental medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to evaluate the effect of switching from tobacco smoking to vaping on gingival health

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

taoc increased.

Key secondary outcomes


Base

Study type

Interventional


Study design

Basic design

n-of-1

Randomization

Randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Diagnosis

Type of intervention

Other

Interventions/Control_1

smoking

Interventions/Control_2

vaping

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

65 years-old >=

Gender

Male and Female

Key inclusion criteria

smokers

Key exclusion criteria

having an acute illness that required treatment (subjects who had a viral infection) within 4 weeks before the enrolment visit, having oral soft tissue disease or any type of gingival overgrowth other than those caused by plaque, suffering from periodontitis, having a history of tooth loss due to periodontitis, being treated with anticoagulant therapy in the previous six months, using prostheses or orthodontic appliances, history of alcoholism or drug/chemical abuse, taking any drug or substance (other than tobacco) that interferes with the cyclooxygenase pathway (e.g. anti-inflammatory drugs including aspirin and ibuprofen) in the 14 days prior to the enrolment visit, taking antibiotics in the 14 days prior to the enrolment visit, breastfeeding or pregnant women.

Target sample size

34


Research contact person

Name of lead principal investigator

1st name indra
Middle name mustikasetia
Last name pribadi

Organization

universitas Padjadjaran

Division name

periodonsia

Zip code

40134

Address

sekeloa selatan no 1 Bandung west java Indonesia

TEL

+628562143662

Email

indra.mustika@unpad.ac.id


Public contact

Name of contact person

1st name Indra
Middle name Mustikasetia
Last name Pribadi

Organization

Universitas Padjadjaran

Division name

Periodonsia

Zip code

40134

Address

Sekeloa selatan no 1 Bandung west java Indonesia

TEL

+628562143662

Homepage URL


Email

indra.mustika@unpad.ac.id


Sponsor or person

Institute

Universitas Padjadajaran

Institute

Department

Personal name



Funding Source

Organization

universitas Padjadjaran and Smile study project

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

Universitas Padjadjaran

Address

sekeloa selatan no 1 Bandung West java Indonesia

Tel

+628562143662

Email

indra.mustika@unpad.ac.id


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

2023 Year 07 Month 21 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

34

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

2022 Year 07 Month 01 Day

Date of IRB

2022 Year 07 Month 10 Day

Anticipated trial start date

2022 Year 07 Month 10 Day

Last follow-up date

2022 Year 12 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2023 Year 07 Month 21 Day

Last modified on

2023 Year 07 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058981


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name