UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status No longer recruiting
Unique ID issued by UMIN UMIN000036847
Receipt No. R000041783
Scientific Title Association of Iliacus Muscle Enlargement with Blood Transfusion in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Date of disclosure of the study information 2019/05/25
Last modified on 2019/07/12

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title Association of Iliacus Muscle Enlargement with Blood Transfusion in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Acronym Association of Iliacus Muscle Enlargement with Blood Transfusion in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Scientific Title Association of Iliacus Muscle Enlargement with Blood Transfusion in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Scientific Title:Acronym Association of Iliacus Muscle Enlargement with Blood Transfusion in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Region
Japan

Condition
Condition Hip fracture(Femoral neck fracture, Trochanteric fracture)
Classification by specialty
Geriatrics Orthopedics Operative medicine
Blood transfusion Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To reveal the association of iliacus muscle enlargemant with blood transfusion after injury in the acute hip fracture patient.
Basic objectives2 Others
Basic objectives -Others To reveal the association of iliacus muscle enlargemant with blood transfusion after injury in the acute hip fracture patient.
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Blood transfusion after injury.
Key secondary outcomes Hemoglobin level on admission.

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
65 years-old <=
Age-upper limit
100 years-old >
Gender Male and Female
Key inclusion criteria 1.Hospitalized patients of femoral neck fracture or femoral trochanteric fracture.
2.CT scan was conducted in a week after injury.
Key exclusion criteria 1.High energy injury(ex. traffic accident),or multiple trauma.
2.With other fracture.
3.With a hemorrhagic event during hospitalization(ex. organ hemorrhage, reoperation).
4.Basicervical fracture or periprosthetic fracture.
5.Patients who have no surgery.
Target sample size 450

Research contact person
Name of lead principal investigator
1st name Takeru
Middle name
Last name Yokota
Organization Iwaki city medical center
Division name Orthopedics
Zip code 973-8555
Address 16chi, Uchigo Mimayamachi Kusehara, Iwaki Shi, Fukushima Ken, 973-8402, Japan
TEL 0246263151
Email yokota_ishi_takeru@yahoo.co.jp

Public contact
Name of contact person
1st name Takeru
Middle name
Last name Yokota
Organization Iwaki city medical center
Division name Orthopedics
Zip code 973-8555
Address 16chi, Uchigo Mimayamachi Kusehara, Iwaki Shi, Fukushima Ken, 973-8402, Japan
TEL 0246263151
Homepage URL
Email yokota_ishi_takeru@yahoo.co.jp

Sponsor
Institute Iwaki city medical center
Institute
Department

Funding Source
Organization None
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 Iwaki city medical center
Address 16chi, Uchigo Mimayamachi Kusehara, Iwaki Shi, Fukushima Ken, 973-8402, Japan
Tel 0246263151
Email yokota_ishi_takeru@yahoo.co.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 いわき市医療センター(福島県)

Other administrative information
Date of disclosure of the study information
2019 Year 05 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 No longer recruiting
Date of protocol fixation
2019 Year 04 Month 01 Day
Date of IRB
2019 Year 07 Month 11 Day
Anticipated trial start date
2014 Year 01 Month 01 Day
Last follow-up date
2017 Year 12 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information Retrospective cohort study

Management information
Registered date
2019 Year 05 Month 25 Day
Last modified on
2019 Year 07 Month 12 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041783

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.