UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036847
Receipt number R000041783
Scientific Title Association of Iliacus Muscle Enlargement with Anemia in the Acute Hip Fracture Patient: a Retrospective Cohort Study
Date of disclosure of the study information 2019/05/25
Last modified on 2021/05/25 00:53:22

* 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 Anemia in the Acute Hip Fracture Patient: a Retrospective Cohort Study

Acronym

Association of Iliacus Muscle Enlargement with Anemia in the Acute Hip Fracture Patient: a Retrospective Cohort Study

Scientific Title

Association of Iliacus Muscle Enlargement with Anemia in the Acute Hip Fracture Patient: a Retrospective Cohort Study

Scientific Title:Acronym

Association of Iliacus Muscle Enlargement with Anemia 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 anemia after injury in the acute hip fracture patient.

Basic objectives2

Others

Basic objectives -Others

To reveal the association of iliacus muscle enlargemant with anemia after injury in the acute hip fracture patient.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Hemoglobin level on admission.

Key secondary outcomes

1. Hemoglobin levels(preoperative, postoperative, at discharge).
2. Amount of transfusion.


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.Fracture type is AO type 31A3, 31B23, 31B3.
5.Periprosthetic fracture.
6.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 or person

Institute

Iwaki city medical center

Institute

Department

Personal name



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

2021 Year 05 Month 25 Day



Link to view the page

Value
https://center6.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