UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055669
Receipt number R000063617
Scientific Title A multicenter prospective observational study of clinical outcome and prognostic factors of fragility fractures of the pelvis
Date of disclosure of the study information 2024/12/01
Last modified on 2026/02/01 09:03:57

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Basic information

Public title

A multicenter prospective observational study of clinical outcome and prognostic factors of fragility fractures of the pelvis

Acronym

A multicenter prospective observational study of clinical outcome and prognostic factors of fragility fractures of the pelvis

Scientific Title

A multicenter prospective observational study of clinical outcome and prognostic factors of fragility fractures of the pelvis

Scientific Title:Acronym

A multicenter prospective observational study of clinical outcome and prognostic factors of fragility fractures of the pelvis

Region

Japan


Condition

Condition

fragility fractures of the pelvis

Classification by specialty

Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

An objective of this study is to investigate the factors influencing clinical outcomes in fragility fractures of the pelvis.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

mortality

Key secondary outcomes

Majeed pelvic score, Barthel Index, living situation


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


Not applicable

Gender

Male and Female

Key inclusion criteria

fragility fractures of the pelvis

Key exclusion criteria

Not applicable

Target sample size

400


Research contact person

Name of lead principal investigator

1st name Koichi
Middle name
Last name Sairyo

Organization

Tokushima University Hospital

Division name

Department of Orthopaedic Surgery

Zip code

770-8503

Address

3-18-15 Kuramoto, Tokushima, Tokushima, Japan

TEL

0886337240

Email

ksairyo@tokushima-u.ac.jp


Public contact

Name of contact person

1st name Keizo
Middle name
Last name Wada

Organization

Tokushima University Hospital

Division name

Department of Orthopaedic Surgery

Zip code

770-8503

Address

3-18-15 Kuramoto, Tokushima, Tokushima, Japan

TEL

0886337240

Homepage URL


Email

wada.keizou@tokushima-u.ac.jp


Sponsor or person

Institute

Tokushima University Hospital

Institute

Department

Personal name



Funding Source

Organization

self funding

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

The Ethics Committee of Tokushima University Hospital

Address

2-50-1 Kuramoto, Tokushima, Tokushima, Japan

Tel

0886158512

Email

first-ec@tokushima-u.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 12 Month 01 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

2024 Year 11 Month 25 Day

Date of IRB

2024 Year 11 Month 25 Day

Anticipated trial start date

2024 Year 12 Month 01 Day

Last follow-up date

2028 Year 12 Month 31 Day

Date of closure to data entry

2028 Year 12 Month 31 Day

Date trial data considered complete


Date analysis concluded



Other

Other related information

An objective of this study is to investigate the factors influencing clinical outcomes in fragility fractures of the pelvis.


Management information

Registered date

2024 Year 09 Month 29 Day

Last modified on

2026 Year 02 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063617