UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000037462 |
|---|---|
| Receipt number | R000042709 |
| Scientific Title | Study on influence on intraoral sense (taste and the sense of touch) of nitrous oxide for healthy adults |
| Date of disclosure of the study information | 2019/08/01 |
| Last modified on | 2021/01/26 18:24:57 |
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Basic information
Public title
Study on influence on intraoral sense (taste and the sense of touch) of the laughing gas for healthy adults
Acronym
Influence on intraoral sense of the laughing gas
Scientific Title
Study on influence on intraoral sense (taste and the sense of touch) of nitrous oxide for healthy adults
Scientific Title:Acronym
Influence on intraoral sense of nitrous oxide
Region
| Japan |
Condition
Condition
Dental phobia
Classification by specialty
| Dental medicine | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Nitrous oxide is discovered and is going to greet 250 years. Nitrous oxide was effective in the "painkilling" "sedation" "poor memory" and has been used for initial first aid at the time of delivery in dental treatment all over the world. By the dental treatment, many patients who came held uneasiness, strain, fear, the unpleasant feelings such as the pain, and such feelings have been used expecting an effect of the "sedation" "poor memory" among other things to enlarge the risk such as the aggravation of complications much less the resistance to the dental treatment of the patient. Nitrous oxide is shown to act on hearing and the sense of touch, optic restraint in a past study, but the influence on taste is not apparent. I have a sense of fear for the intraoral sense (taste and the sense of touch) except the sense of pain to feel during dental treatment in the dental phobia patient and may lead to a refusal action. It is intended that I clarify it about usefulness of the nitrous oxide use to a dental treatment patient by inspecting the effect to an intraoral sense of the nitrous oxide in this study.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
I obtain its consent with predetermined written consent at the time of a study cooperation request. I let a target person obtained its consent reply a young man, an adult sense profile and a questionnaire.
Under 0% of laughing gas (nitrous oxide), 20%, 30%, 50%, 70%, I carry out following experiments.
1.Blood pressure, the pulse, temperature, ventilatory frequency, the measurement of the percutaneous arterial blood oxygen saturation
2.Judgment (Ramsay score) of the sedation degree by the sedation score
3.The measurement (a mental stress activates excitement of the sympathetic system, and amylase activity increases as an internal self-defense reaction.) of saliva amylase
4.Examination of electric pulpal stimulation (A-delta fiber of four or five maxillary pulps, the threshold measurement by the C fiber stimulation)
5.The measurement of the surface of a body ache by the perception meter (10-20 g) and the oral pain
6.Examination of taste with the electric taste meter
7.Examination of taste with the reagent for examinations for taste qualitative fixed-quantity of the filter paper disk (sweetness, saltiness, acidity, bitterness)
8.Examination for R-R distance (examination of heart rate change)
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
| 40 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
The person that I performed written informed consent by the adult volunteer including the student of Kyushu Dental College, and consent was provided.
Key exclusion criteria
The person who corresponds to a taboo of the laughing gas. Or the person that a case and the agreement that had difficulty in understanding of study contents were not provided.
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | NOZOMU |
| Middle name | |
| Last name | HARANO |
Organization
Kyushu Dental University
Division name
Dental Anesthesiology
Zip code
803-8580
Address
2-6-1, manaduru, kokurakitaku, kitakyushu city, Fukuoka, Japan
TEL
093-581-1131
harano@kyu-dent.ac.jp
Public contact
Name of contact person
| 1st name | Nozomu |
| Middle name | |
| Last name | Harano |
Organization
Kyushu Dental University
Division name
Dental Anesthesiology
Zip code
803-8580
Address
2-6-1, manaduru, kokurakitaku, kitakyushu city, Fukuoka, Japan
TEL
093-581-1131
Homepage URL
harano@kyu-dent.ac.jp
Sponsor or person
Institute
Kyushu Dental University
Institute
Department
Personal name
Funding Source
Organization
Japan Science and Technology Agency
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Kyushu Dental University
Address
2-6-1, manaduru, kokurakitaku, kitakyushu city, Fukuoka, Japan
Tel
093-701-9551
harano@kyu-dent.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
| 2019 | Year | 08 | 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
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 | 04 | Month | 09 | Day |
Date of IRB
| 2019 | Year | 06 | Month | 03 | Day |
Anticipated trial start date
| 2019 | Year | 07 | Month | 01 | Day |
Last follow-up date
| 2019 | Year | 12 | Month | 01 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
There is no Important Notice.
Management information
Registered date
| 2019 | Year | 07 | Month | 24 | Day |
Last modified on
| 2021 | Year | 01 | Month | 26 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042709
| Research Plan | |
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| Registered date | File name |
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