UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000009575
Receipt number R000011233
Scientific Title Efficacy and safety analysis of monthly minodronic acid in Japanese osteoporotic patients switched from traditional bisphosphonates
Date of disclosure of the study information 2012/12/18
Last modified on 2018/03/08 08:40:24

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Basic information

Public title

Efficacy and safety analysis of monthly minodronic acid in Japanese osteoporotic patients switched from traditional bisphosphonates

Acronym

Usefulness of switching to monthly minodronic acid in Japanese osteoporotic patients

Scientific Title

Efficacy and safety analysis of monthly minodronic acid in Japanese osteoporotic patients switched from traditional bisphosphonates

Scientific Title:Acronym

Usefulness of switching to monthly minodronic acid in Japanese osteoporotic patients

Region

Japan


Condition

Condition

Osteoporosis

Classification by specialty

Medicine in general Endocrinology and Metabolism Clinical immunology
Geriatrics Obstetrics and Gynecology Orthopedics
Radiology Laboratory medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the usefulness of switching to
monthly minodronic acid in Japanese osteoporotic patients who were taking traditional bisphosphonates (BPs). –Six months intervention study

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Bone mineral density
Bone turnover marker

Key secondary outcomes

Low back pain
Abdominal symptoms
Preference and adherence for BPs
Osteoporotic fracture


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Minodronic acid (50mg/month)

Interventions/Control_2

Another BPs

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

1. Patients with osteoporosis
2. Patients who were taking traditional BPs
3. Patients giving informed consent

Key exclusion criteria

Patients with
1. Esophageal stricture or achalasia
2. Incapability in remaining upright for 30 min
3.Hypersensitivity to minodronic acid and other bisphosphonates
4. Hypocalcemia
5. Pregnancy
6. Aphagia, Esophagitis, Gastritis, Duodenitis or Ulcers
7. Severe renal dysfunction

Target sample size

600


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Satoshi Ikeda

Organization

Ken-Ai Memorial Hospital

Division name

Department of Orthopedic Surgery

Zip code


Address

1191 Oaza Kimori, Onga-Machi, Onga-Gun Fukuoka, 811-4313 Japan

TEL

093-293-7090

Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Ken-Ai Memorial Hospital

Division name

Department of Orthopedic Surgery

Zip code


Address


TEL


Homepage URL


Email

s-ikeda@med.uoeh-u.ac.jp


Sponsor or person

Institute

Ken-Ai Memorial Hospital

Institute

Department

Personal name



Funding Source

Organization

Astellas Pharma Inc.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Sanzai Hospital
Tsurukami Orthopaedic and Rheumatoid Clinic
Kitakyushu General Hospital
Makiyama Chuou Hospital
Obase Hospital
Katsuki Neurosurgery and Orthopaedic Clinic

Name of secondary funder(s)


Teshima Orthopaedic Clinic
Okimoto Clinic
Sakamidorii Hospital
Okamoto Orthopaedic Clinic


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



Other administrative information

Date of disclosure of the study information

2012 Year 12 Month 18 Day


Related information

URL releasing protocol


Publication of results

Published


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

2011 Year 09 Month 28 Day

Date of IRB


Anticipated trial start date

2011 Year 10 Month 01 Day

Last follow-up date

2014 Year 09 Month 30 Day

Date of closure to data entry

2014 Year 09 Month 30 Day

Date trial data considered complete

2014 Year 09 Month 30 Day

Date analysis concluded

2014 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2012 Year 12 Month 18 Day

Last modified on

2018 Year 03 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011233


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name