UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055989
Receipt number R000063404
Scientific Title A study to verify the usefulness of telemedicine in the field of hand surgery
Date of disclosure of the study information 2024/10/30
Last modified on 2024/10/30 12:33:25

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Basic information

Public title

A study to verify the usefulness of telemedicine in the field of hand surgery

Acronym

A study to verify the usefulness of telemedicine in the field of hand surgery

Scientific Title

A study to verify the usefulness of telemedicine in the field of hand surgery

Scientific Title:Acronym

telemedicine in the field of hand surgery

Region

Japan


Condition

Condition

Lateral humeral epicondylitis, de Quervain tendonitis, carpal tunnel syndrome, trauma

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

telemedicine can be used in the field of hand surgery

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Questionnaire for doctors

Key secondary outcomes

Questionnaire for patients


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Maneuver

Interventions/Control_1

telemedicine

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

Lateral humeral epicondylitis, de Quervain tendonitis, carpal tunnel syndrome, trauma

Key exclusion criteria

Patients who are unable to respond to questionnaires due to mental illness, inability to speak Japanese, etc.
Patients who have fresh wounds on their upper limbs and cannot use equipment

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Michiro
Middle name
Last name Yamamoto

Organization

Nagoya University

Division name

Hand Surgery

Zip code

4668550

Address

65Turumai Shouwaku Nagoya

TEL

052-744-2965

Email

michi-ya@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Michiro
Middle name
Last name Yamamotp

Organization

Nagoya Universiy

Division name

Hand Surgery

Zip code

466-8550

Address

65 Turumai Showaku Nagoya

TEL

052-744-2965

Homepage URL


Email

michi-ya@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name



Funding Source

Organization

NEDO

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

Nagoya University

Address

65 Turumai SHowaku Nagoya

Tel

052-744-2111

Email

ethics@med.nagoya-u.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

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


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

Preinitiation

Date of protocol fixation

2024 Year 10 Month 30 Day

Date of IRB


Anticipated trial start date

2024 Year 12 Month 01 Day

Last follow-up date

2029 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 10 Month 30 Day

Last modified on

2024 Year 10 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063404