UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054686
Receipt number R000062494
Scientific Title Analysis of the effect of wearing elastic stockings during the day to improve nocturnal polyuria
Date of disclosure of the study information 2024/06/17
Last modified on 2025/03/03 16:30:46

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Basic information

Public title

Analysis of the effect of wearing elastic stockings during the day to improve nocturnal polyuria

Acronym

Analysis of the effect of wearing elastic stockings during the day to improve nocturnal polyuria

Scientific Title

Analysis of the effect of wearing elastic stockings during the day to improve nocturnal polyuria

Scientific Title:Acronym

Analysis of the effect of wearing elastic stockings during the day to improve nocturnal polyuria

Region

Japan


Condition

Condition

nocturnal polyuria

Classification by specialty

Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to evaluate whether or not elastic stockings can improve nocturia and polyuria in patients with nocturnal polyuria.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Change in nocturnal urine volume with and without elastic stockings.

Key secondary outcomes



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

Treatment

Type of intervention

Other

Interventions/Control_1

Wearing elastic stockings for 3 days to 1 week (daytime only)

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

40 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) Over 40 years old.
(2) Patients with nocturia due to nocturnal polyuria who visit (or are hospitalized at) our hospital and collaborating institutions.
(3) Patients with spontaneous voiding: urinate at least twice between going to bed and waking up.
Patients with indwelling urinary catheters: nocturnal urine output greater than 1/3 of daily urine output.

Key exclusion criteria

(1) Patients who do not wish to participate in this study.
(2) Patients deemed by the investigator to be ineligible for the study.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Mitsuru
Middle name
Last name Noguchi

Organization

Saga University Hospital

Division name

Urology

Zip code

849-8501

Address

5-1-1, Nabeshima, Saga City, Saga Prefecture

TEL

0952-34-2344

Email

nogman@cc.saga-u.ac.jp


Public contact

Name of contact person

1st name Shohei
Middle name
Last name Tobu

Organization

Saga University Hospital

Division name

Urology

Zip code

849-8501

Address

5-1-1, Nabeshima, Saga City, Saga Prefecture

TEL

0952-34-2344

Homepage URL


Email

toubu7@cc.saga-u.ac.jp


Sponsor or person

Institute

Saga University

Institute

Department

Personal name



Funding Source

Organization

IIDA HOSIERY CO. LTD.

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

Clinical Research Ethics Committee of Saga University Hospital

Address

5-1-1, Nabeshima, Saga City, Saga Prefecture

Tel

0952-34-3357

Email

kenkyu-shinsei@ml.cc.saga-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 06 Month 17 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 02 Month 14 Day

Date of IRB

2023 Year 06 Month 05 Day

Anticipated trial start date

2023 Year 06 Month 05 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



Management information

Registered date

2024 Year 06 Month 17 Day

Last modified on

2025 Year 03 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062494