UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000052484 |
|---|---|
| Receipt number | R000059898 |
| Scientific Title | Effect of Kinesio Taping and Compression Taping on Facial Swelling After Orthognathic Surgery |
| Date of disclosure of the study information | 2023/10/13 |
| Last modified on | 2023/10/13 12:46:39 |
* 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
Effect of Kinesio Taping and Compression Taping on Facial Swelling After Orthognathic Surgery
Acronym
Effect of Kinesio Taping and Compression Taping on Facial Swelling After Orthognathic Surgery
Scientific Title
Effect of Kinesio Taping and Compression Taping on Facial Swelling After Orthognathic Surgery
Scientific Title:Acronym
Effect of Kinesio Taping and Compression Taping on Facial Swelling After Orthognathic Surgery
Region
| Japan |
Condition
Condition
Jaw deformity
Classification by specialty
| Oral surgery | Dental medicine | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To determine the inhibitory effect of compression tape and kinesio taping using the Epidermis, Dermis, and Fascia method on postoperative swelling of jaw deformities.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
swelling volume, body surface temperature
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -participants are blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Treatment
Type of intervention
| Device,equipment | Maneuver |
Interventions/Control_1
Taping the participants with Kinesio tape.
Interventions/Control_2
Compression taping on participants.
Interventions/Control_3
No taping
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
| 60 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
1. Participants who agreed with the study purpose and experimental procedures of this study.
2. Participants who have consented to participate in this study.
3. Participants who have signed an informed consent form.
Key exclusion criteria
1.Patients with hemorrhagic predisposition,
2.Patients with postoperative factor 13 deficiency,
3.Postoperative infection,
4.Patients with Le Fort 1 osteotomy only,
5.patients who underwent concomitant genioplasty
Target sample size
150
Research contact person
Name of lead principal investigator
| 1st name | Shogo |
| Middle name | |
| Last name | Hasegawa |
Organization
School of Dentistry, Aichi Gakuin University Graduate School of Medicine
Division name
Department of Maxillofacial Surgery
Zip code
464-8651
Address
2-11, Suemori-Dori, Chikusa-ku, Nagoya 464-8651, Japan
TEL
052-759-2160
shogo@dpc.aichi-gakuin.ac.jp
Public contact
Name of contact person
| 1st name | Shogo |
| Middle name | |
| Last name | Hasegawa |
Organization
School of Dentistry, Aichi Gakuin University Graduate School of Medicine
Division name
Department of Maxillofacial Surgery
Zip code
464-8651
Address
2-11, Suemori-Dori, Chikusa-ku, Nagoya 464-8651, Japan
TEL
052-759-2160
Homepage URL
shogo@dpc.aichi-gakuin.ac.jp
Sponsor or person
Institute
Department of Maxillofacial Surgery School of Dentistry, Aichi Gakuin University Graduate School of Medicine
Institute
Department
Personal name
Funding Source
Organization
No special note
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
Department of Maxillofacial Surgery, School of Dentistry, Aichi Gakuin University Graduate School of Medicine
Address
Suemori-Dori, Chikusa-ku, Nagoya 464-8651, Japan
Tel
052-759-2160
shogo@dpc.aichi-gakuin.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
| 2023 | Year | 10 | Month | 13 | 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
105
Results
Postoperative swelling was measured at 3, 7, 30, and 90 days postoperatively to compare the kinesio tape group, compression tape group, and control group, and no significant differences were found in postoperative swelling between the groups at each time point. Subgroup analysis by surgical technique also showed no significant differences between the groups at each time point. There was no significant difference in postoperative body surface temperature between the groups.
Results date posted
| 2023 | Year | 10 | Month | 13 | Day |
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
105 healthy male and female patients diagnosed with jaw deformities and underwent orthognathic surgery
Participant flow
Of 162 patients diagnosed with jaw deformities who underwent orthognathic surgery, 105 patients were included in the study after exclusion of patients with bleeding predisposition, genioplasty, and maxilloplasty alone, and after obtaining necessary data.
Patients were randomly divided into 3 groups: EDF-KT group, CT group, and no tape (group C).
Adverse events
No special note
Outcome measures
Swelling volume, body surface temperature
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2020 | Year | 04 | Month | 05 | Day |
Date of IRB
| 2019 | Year | 04 | Month | 09 | Day |
Anticipated trial start date
| 2023 | Year | 10 | Month | 13 | Day |
Last follow-up date
| 2024 | Year | 10 | Month | 13 | 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 | 10 | Month | 13 | Day |
Last modified on
| 2023 | Year | 10 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000059898
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
|---|---|
| Registered date | File name |
| Research case data | |
|---|---|
| Registered date | File name |
