UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010239
Receipt number R000011962
Scientific Title Estimation of platelet-rich fibrin on prevention of bisphosphonate-related osteonecrosis of the jaw
Date of disclosure of the study information 2013/04/01
Last modified on 2015/05/12 11:29:49

* 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

Estimation of platelet-rich fibrin on prevention of bisphosphonate-related osteonecrosis of the jaw

Acronym

Estimation of platelet-rich fibrin on prevention of bisphosphonate-related osteonecrosis of the jaw

Scientific Title

Estimation of platelet-rich fibrin on prevention of bisphosphonate-related osteonecrosis of the jaw

Scientific Title:Acronym

Estimation of platelet-rich fibrin on prevention of bisphosphonate-related osteonecrosis of the jaw

Region

Japan


Condition

Condition

bisphosphonate-related osteonecrosis of the jaw

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety and efficacy of platelet-rich fibrin on wound healing and bone regeneration of tooth extraction in a patient receiving oral bisphosphonate therapy.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase



Assessment

Primary outcomes

percentage of the cases without impaired healing of socket
The incidence of adverse event

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver Other

Interventions/Control_1

A total of 10 subjects,3 months study.
a patientreceiving oral bisphosphonate therapy for not less than 1 year.
platelet-fibrin is separated from blood and plugged into extraction socket.

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


Not applicable

Gender

Male and Female

Key inclusion criteria

a patient receiving oral bisphosphonate therapy for not less than 1 year.
a patient who needs to extract teeth

Key exclusion criteria

poor general condition
a patients who is difficult to visit our hospital for 3 months after tooth extraction.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takuya Asaka

Organization

Hokkaido University

Division name

Graduate School of Dental Medicine

Zip code


Address

Kita-13, Nishi-7, Kita-ku, Sapporo 060-8586

TEL

011-706-4280

Email

asakatakuya@den.hokudai.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takuya Asaka

Organization

Hokkaido University

Division name

Graduate School of Dental Medicine

Zip code


Address

Kita-13, Nishi-7, Kita-ku, Sapporo 060-8586

TEL

011-706-4280

Homepage URL


Email

asakatakuya@den.hokudai.ac.jp


Sponsor or person

Institute

Hokkaido University

Institute

Department

Personal name



Funding Source

Organization

Hokkaido University

Organization

Division

Category of Funding Organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

北海道大学病院


Other administrative information

Date of disclosure of the study information

2013 Year 04 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

Completed

Date of protocol fixation

2013 Year 03 Month 04 Day

Date of IRB


Anticipated trial start date

2013 Year 04 Month 01 Day

Last follow-up date

2015 Year 04 Month 30 Day

Date of closure to data entry

2015 Year 04 Month 30 Day

Date trial data considered complete

2015 Year 04 Month 30 Day

Date analysis concluded

2015 Year 04 Month 30 Day


Other

Other related information



Management information

Registered date

2013 Year 03 Month 13 Day

Last modified on

2015 Year 05 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011962


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name