UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022054
Receipt number R000025414
Scientific Title The observational study of the incidence of respiratory depression induced by intrathecal or epidural morphine in Cesarean section
Date of disclosure of the study information 2016/04/25
Last modified on 2019/10/31 11:26:27

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Basic information

Public title

The observational study of the incidence of respiratory depression induced by intrathecal or epidural morphine in Cesarean section

Acronym

The respiratory depression of intrathecal or epidural morphine

Scientific Title

The observational study of the incidence of respiratory depression induced by intrathecal or epidural morphine in Cesarean section

Scientific Title:Acronym

The respiratory depression of intrathecal or epidural morphine

Region

Japan


Condition

Condition

status after Cesarean section

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to clarify the incidence of respiratory depression induced by intrathecal or epidural morphine in Cesarean section

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

the incidence of respiratory depression from just after operation to 9 am postoperative day 1

Key secondary outcomes

the problem and adverse event of this device


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

50 years-old >=

Gender

Female

Key inclusion criteria

post-cesarean patient administered intrathecal or epidural morphine

Key exclusion criteria

Off-label use for intrathecal and epidural anesthesia
contraindication of morphine administeration
patient who managed by respirator

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Shingo
Middle name
Last name Irikoma

Organization

Seirei Hamamatsu General Hospital

Division name

Department of Anesthesiology

Zip code

43008558

Address

2-12-12, Sumiyoshi, Naka-ku, Hamamatsu City

TEL

053-474-2222

Email

s.irikoma@gmail.com


Public contact

Name of contact person

1st name Shingo
Middle name
Last name Irikoma

Organization

Seirei Hamamatsu General Hospital

Division name

Department of Anesthesiology

Zip code

4308558

Address

2-12-12, Sumiyoshi, Naka-ku, Hamamatsu City

TEL

053-474-2222

Homepage URL


Email

s.irikoma@gmail.com


Sponsor or person

Institute

Seirei Hamamatsu General Hospital

Institute

Department

Personal name



Funding Source

Organization

Nothing

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor

National Center for Child Health and Development

Name of secondary funder(s)



IRB Contact (For public release)

Organization

IRB in Seirei Hamamatsu General Hospital

Address

2-12-12, Sumiyoshi, Naka-ku, Hamamatsu City

Tel

0534742222

Email

s.irikoma@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



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2016 Year 04 Month 25 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

Completed

Date of protocol fixation

2015 Year 10 Month 29 Day

Date of IRB

2016 Year 04 Month 25 Day

Anticipated trial start date

2016 Year 04 Month 25 Day

Last follow-up date

2019 Year 04 Month 25 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2017 Year 08 Month 31 Day


Other

Other related information

We will write a scientific article as soon as possible after finishing this study.


Management information

Registered date

2016 Year 04 Month 25 Day

Last modified on

2019 Year 10 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025414


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name