UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000058972
Receipt number R000067440
Scientific Title Research on orofacial myofunctional therapy in patients with cleft lip and palate
Date of disclosure of the study information 2025/12/31
Last modified on 2025/09/02 21:16:07

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Basic information

Public title

Research on orofacial myofunctional therapy in patients with cleft lip and palate

Acronym

Research on orofacial myofunctional therapy in patients with cleft lip and palate

Scientific Title

Research on orofacial myofunctional therapy in patients with cleft lip and palate

Scientific Title:Acronym

Research on orofacial myofunctional therapy in patients with cleft lip and palate

Region

Japan


Condition

Condition

Cleft lip,Cleft lip and jaw,Cleft lip and palate,Cleft palate

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To implement myofunctional therapy in patients with cleft lip and palate and to clarify its effectiveness and characteristics across different ages.

Basic objectives2

Others

Basic objectives -Others

Patients with cleft lip and palate undergo treatments such as cheiloplasty, palatoplasty, and orthodontics to restore morphology. Although oral functions have been studied extensively, the effectiveness of orofacial myofunctional therapy is still unclear. This study therefore aimed to examine the effectiveness of orofacial myofunctional therapy in patients with cleft lip and palate.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Myofunctional therapy was performed for a total of three months, and lip-closing strength was measured monthly.

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

4 years-old <=

Age-upper limit

12 years-old >=

Gender

Male and Female

Key inclusion criteria

(1)Disease name:Cleft lip,Cleft lip and jaw,Cleft lip and palate,Cleft palate
(2)Age: 4 years old or older, 13 years old or younger
(3) Gender: Male and female
(4) Those who have obtained written consent on behalf of their guardians for research participation.

Key exclusion criteria

(1)Patients with other congenital abnormalities
(2)Other patients deemed inappropriate by the research director

Target sample size

45


Research contact person

Name of lead principal investigator

1st name hiroyasu
Middle name
Last name kanetaka

Organization

Tohoku University Graduate of Dentistry

Division name

Department of Orthodontics

Zip code

980-8575

Address

4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi Prefecture

TEL

022-717-8374

Email

hiroyasu.kanetaka.e6@tohoku.ac.jp


Public contact

Name of contact person

1st name kasumi
Middle name
Last name hasegawa

Organization

Tohoku University Graduate of Dentistry

Division name

Craniofacial Anomalies

Zip code

980-8575

Address

4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi Prefecture

TEL

022-7171-8277

Homepage URL


Email

kawamura.kasumi.p4@dc.tohoku.ac.jp


Sponsor or person

Institute

other

Institute

Department

Personal name



Funding Source

Organization

other

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

Tohoku University Graduate of Dentistry

Address

4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi Prefecture

Tel

0227178379

Email

kawamura.kasumi.p4@dc.tohoku.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

2025 Year 12 Month 31 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

Open public recruiting

Date of protocol fixation

2025 Year 08 Month 13 Day

Date of IRB

2025 Year 08 Month 13 Day

Anticipated trial start date

2025 Year 08 Month 13 Day

Last follow-up date

2028 Year 10 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Target audience
:Among patients attending Tohoku University Hospital Department of Oral and Maxillofacial Functional Treatment, men and women aged 4 years and under 12 with cleft lip, cleft lip and jaw, cleft lip and palate, or cleft palate or above.
Measurement item
:Lip pressure


Management information

Registered date

2025 Year 09 Month 02 Day

Last modified on

2025 Year 09 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067440