UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000023673
Receipt number R000027255
Scientific Title Comparison of effects of BD Micro Fine Plus and NANOPASS Needle II in diabetic patients with insulin therapy
Date of disclosure of the study information 2016/08/19
Last modified on 2019/02/20 10:27:53

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Basic information

Public title

Comparison of effects of BD Micro Fine Plus and NANOPASS Needle II in diabetic patients with insulin therapy

Acronym

Comparison of effects of 32G 4mm and 34G 4mm insulin pen needle in diabetic patients with insulin therapy

Scientific Title

Comparison of effects of BD Micro Fine Plus and NANOPASS Needle II in diabetic patients with insulin therapy

Scientific Title:Acronym

Comparison of effects of 32G 4mm and 34G 4mm insulin pen needle in diabetic patients with insulin therapy

Region

Japan


Condition

Condition

Diabetes

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to compare the puncture site pain between 32G 4mm needle (BD Micro Fine Plus) and 34G 4mm needle (NANOPASS Needle II).

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Assessment of puncture site pain using the visual analogue scale

Key secondary outcomes

HbA1c, Adverse events (dribbling, bleeding, needle breakage)


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

Device,equipment

Interventions/Control_1

After obtaining informed consent from all patients, they switched from 32G 4mm needles to 34G 4mm needles.

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

Diabetic patients who perform self-injection of insulin with pen injectors.

Key exclusion criteria

Patients who have trouble determining the pain intensity, or any other criterion associated with the questionnaire.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tsunehiko Yamamoto

Organization

Kansai Rosai Hospital

Division name

Diabetes and Endocrinology

Zip code


Address

3-1-69, Inabaso, Amagasaki city, Hyogo

TEL

06-6416-1221

Email

tsunehiko@sannet.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Daisuke Saito

Organization

Kansai Rosai Hospital

Division name

Diabetes and Endocrinology

Zip code


Address

3-1-69, Inabaso, Amagasaki city, Hyogo

TEL

06-6416-1221

Homepage URL


Email

dsaitou@juntendo.ac.jp


Sponsor or person

Institute

Kansai Rosai Hospital

Institute

Department

Personal name



Funding Source

Organization

none

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


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

2016 Year 08 Month 19 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

2016 Year 07 Month 26 Day

Date of IRB


Anticipated trial start date

2016 Year 08 Month 22 Day

Last follow-up date

2017 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 08 Month 18 Day

Last modified on

2019 Year 02 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027255


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name