UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053563
Receipt number R000061060
Scientific Title Development of nursing care products for pain relief around the vulva during ongoing labor
Date of disclosure of the study information 2024/02/07
Last modified on 2024/02/07 09:51:55

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Basic information

Public title

Development of nursing care products for pain relief around the vulva during ongoing labor

Acronym

Development of maternity pain relief care products

Scientific Title

Development of nursing care products for pain relief around the vulva during ongoing labor

Scientific Title:Acronym

Development of maternity pain relief care products

Region

Japan


Condition

Condition

pregnant woman

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study aim to development of nursing care products for pain relief around the vulva.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Effects of using care products

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Use of development care item

Interventions/Control_2

Use of normal care item

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


Not applicable

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

Pregnant women planning to have a natural childbirth

Key exclusion criteria

Pregnant women no planning to have a natural childbirth

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Keiko
Middle name
Last name Mano

Organization

FUJITA HEALTH UNIVERSITY HOSPITAL

Division name

Nursing Department

Zip code

470-1192

Address

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

TEL

0562-93-2111

Email

hp1.nurse@fujita-hu.ac.jp


Public contact

Name of contact person

1st name Akiko
Middle name
Last name Watanabe

Organization

FUJITA HEALTH UNIVERSITY

Division name

Center for Collaboration in Research and Innovation

Zip code

470-1192

Address

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

TEL

0562-93-2111

Homepage URL


Email

fuji-san@fujita-hu.ac.jp


Sponsor or person

Institute

FUJITA HEALTH UNIVERSITY HOSPITAL

Institute

Department

Personal name



Funding Source

Organization

FUJITA HELTH UNIVERSITY

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

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

Address

1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

Tel

0562-93-2111

Email

f-irb@fujita-hu.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 02 Month 07 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

Enrolling by invitation

Date of protocol fixation

2024 Year 01 Month 22 Day

Date of IRB

2024 Year 01 Month 22 Day

Anticipated trial start date

2024 Year 01 Month 23 Day

Last follow-up date

2025 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 02 Month 07 Day

Last modified on

2024 Year 02 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061060


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name