UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057901
Receipt number R000066178
Scientific Title Elucidating the relationship between obstructive sleep apnea and sarcopenia
Date of disclosure of the study information 2025/05/19
Last modified on 2025/05/19 11:18:24

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Basic information

Public title

Elucidating the relationship between obstructive sleep apnea and sarcopenia

Acronym

Elucidating the relationship between obstructive sleep apnea and sarcopenia

Scientific Title

Elucidating the relationship between obstructive sleep apnea and sarcopenia

Scientific Title:Acronym

Elucidating the relationship between obstructive sleep apnea and sarcopenia

Region

Japan


Condition

Condition

No disease

Classification by specialty

Oral surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study was to examine whether there is a relationship between sarcopenia and oral function in elderly OSA

Basic objectives2

Others

Basic objectives -Others

Relationship between sleep apnea and sarcopenia

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Correlation between severity of AHI and oral function

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


Not applicable

Gender

Male and Female

Key inclusion criteria

1. who are scheduled to undergo general anesthesia surgery at this hospital and have undergone perioperative oral management by an oral surgeon
2. who are 65 years of age or older at the time of consent (regardless of gender)
3. who have received a full explanation of the participation in this study, and who have given written consent of their own free will based on full understanding

Key exclusion criteria

1) Patients with central sleep disorders
(2) Patients with dementia
(3) Patients who cannot give consent for the research
(4) Other patients deemed inappropriate as research subjects by the principal investigator

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Yuki
Middle name
Last name Sakamoto

Organization

Kansai medical university medical center

Division name

Oral surgery

Zip code

5708507

Address

10-15Fumizono-cyo Moriguchi-shi Osaka-fu

TEL

0669939420

Email

s.yukioutdoor@gmail.com


Public contact

Name of contact person

1st name Yuki
Middle name
Last name Sakamto

Organization

Kansai medical university medical center

Division name

Oral surgery

Zip code

5708507

Address

10-15 Fumizono-cho Moriguchi-shi

TEL

0669939420

Homepage URL


Email

s.yukioutdoor@gmail.com


Sponsor or person

Institute

Kansai medical university

Institute

Department

Personal name



Funding Source

Organization

Kansai medical university

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

Kansai Medical University Medical Center

Address

10-15 Fumizono-cho Moriguchi-shi

Tel

0669939420

Email

s.yukioutdoor@gmail.com


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW

大阪府


Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2025 Year 05 Month 19 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

2023 Year 08 Month 18 Day

Date of IRB

2023 Year 08 Month 18 Day

Anticipated trial start date

2023 Year 08 Month 22 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

nothing


Management information

Registered date

2025 Year 05 Month 19 Day

Last modified on

2025 Year 05 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066178