UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055994 |
|---|---|
| Receipt number | R000063991 |
| Scientific Title | Patient Satisfaction Survey on Intravenous Sedation in a Dental Anesthesia Clinic |
| Date of disclosure of the study information | 2024/10/30 |
| Last modified on | 2024/10/31 14:53:46 |
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Basic information
Public title
Patient Satisfaction Survey on Intravenous Sedation in a Dental Anesthesia Clinic
Acronym
Patient Satisfaction Survey on Intravenous Sedation in a Dental Anesthesia Clinic
Scientific Title
Patient Satisfaction Survey on Intravenous Sedation in a Dental Anesthesia Clinic
Scientific Title:Acronym
Patient Satisfaction Survey on Intravenous Sedation in a Dental Anesthesia Clinic
Region
| Japan |
Condition
Condition
dental anxiety disorder, hyperactive gag reflex, arterial hypertension, and related conditions
Classification by specialty
| Anesthesiology | Dental medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Intravenous sedation is administered alongside dental treatment for patients with dental anxiety, a hyperactive gag reflex, or systemic conditions requiring special care. Its primary purposes are to reduce anxiety and stabilize hemodynamics; however, some patients experience significant anxiety regarding the sedation itself. This study evaluates patient satisfaction and the effectiveness of intravenous sedation in alleviating anxiety.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Satisfaction Survey(11-point scale: 0-10)
Key secondary outcomes
Anxiety levels pre- and post-treatment (numeric rating scale), sedation depth during procedure (modified observer's assessment of alertness/sedation; MOAA/S score), sedative dosage, patient background information.
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
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Patients who received intravenous sedation for dental treatment between August 2023 and March 2024.
Key exclusion criteria
Patients with intellectual disabilities and those who have difficulty responding to the questionnaire.
Target sample size
300
Research contact person
Name of lead principal investigator
| 1st name | Shigeru |
| Middle name | |
| Last name | Maeda |
Organization
Graduate School of Medical and Dental Science, Institute of Science Tokyo
Division name
Department of Dental Anesthesiology
Zip code
113-8549
Address
1-5-45 Yushima, Bunkyo-Ku, Tokyo
TEL
03-5803-5548
maedas.daop@tmd.ac.jp
Public contact
Name of contact person
| 1st name | Shigeru |
| Middle name | |
| Last name | Maeda |
Organization
Graduate School of Medical and Dental Science, Institute of Science Tokyo
Division name
Department of Dental Anesthesiology
Zip code
113-8549
Address
1-5-45 Yushima, Bunkyo-Ku, Tokyo
TEL
03-5803-5548
Homepage URL
maedas.daop@tmd.ac.jp
Sponsor or person
Institute
Institute of Science Tokyo
Institute
Department
Personal name
Funding Source
Organization
Institute of Science Tokyo
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
Institute of Science Tokyo
Address
1-5-45 Yushima, Bunkyo-Ku, Tokyo
Tel
03-5803-5548
kawauchi.aki@tmd.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
東京科学大学病院（東京都）
Other administrative information
Date of disclosure of the study information
| 2024 | Year | 10 | Month | 30 | 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
300
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
No longer recruiting
Date of protocol fixation
| 2023 | Year | 07 | Month | 10 | Day |
Date of IRB
| 2023 | Year | 07 | Month | 10 | Day |
Anticipated trial start date
| 2023 | Year | 08 | Month | 01 | Day |
Last follow-up date
| 2024 | Year | 12 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
The aim of this study is to investigate patient satisfaction and the effectiveness of intravenous sedation in reducing anxiety in patients undergoing dental treatment.
Management information
Registered date
| 2024 | Year | 10 | Month | 30 | Day |
Last modified on
| 2024 | Year | 10 | Month | 31 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063991
