UMIN-CTR Clinical Trial

Recruitment status Terminated
Unique ID issued by UMIN UMIN000009521
Receipt No. R000011172
Official scientific title of the study Evaluation of Neonatal Adrenal Function in Preterm Infants by Serum and Urine Steroids Assay
Date of disclosure of the study information 2012/12/13
Last modified on 2017/04/24 (Ver. 4)

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Basic information
Official scientific title of the study Evaluation of Neonatal Adrenal Function in Preterm Infants by Serum and Urine Steroids Assay
Title of the study (Brief title) Evaluation of Neonatal Adrenal Function in Preterm Infants by Using Steroids Assay
Region
Japan

Condition
Condition preterm infants
Classification by specialty
Pediatrics
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 The porpose is to be able to properly evaluate the adrenal function in preterm infants and is to set the reference value.
Basic objectives2 Others
Basic objectives -Others The second porpose is to be able to use steroids properly to preterm infants
Trial characteristics_1 Confirmatory
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes A comparison of serum and urine steroids hormon consentration of preterm and term infants.
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

Not applicable
Age-upper limit
7 years-old >=
Gender Male and Female
Key inclusion criteria preterm infants.
term infants as controls.
Key exclusion criteria preterm infants with complications such as heart disease, chromosomal abnormality and so on.
term infants there was some kind of medical intervention.
Target sample size 800

Research contact person
Name of lead principal investigator Tomonobu Hasegawa
Organization Keio University School of Medicine
Division name Departmento of Pediatrics
Address Shinanomachi35, Shinjuku, Tokyo
TEL 0333531211
Email thaseg@z6.keio.jp

Public contact
Name of contact person Masayuki Miwa
Organization Keio University School of Medicine
Division name Departmento of Pediatrics
Address Shinanomachi Shinjuku 35
TEL 03-3353-2071
Homepage URL
Email m38miwa@z2.keio.jp

Sponsor
Institute Department of Pediatrics, Keio University School of Medicine
Institute
Department

Funding Source
Organization Department of Pediatrics, Keio University School of Medicine
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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
2012 Year 12 Month 13 Day

Progress
Recruitment status Terminated
Date of protocol fixation
2012 Year 01 Month 17 Day
Anticipated trial start date
2012 Year 02 Month 10 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Unpublished
URL releasing results
Results This research was terminated before analysis.
Other related information There is stratified analysis according to the presence or absence of steroid administration to preterm infants.

Management information
Registered date
2012 Year 12 Month 11 Day
Last modified on
2017 Year 04 Month 24 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011172