UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000021914
Receipt number R000022971
Scientific Title The study to evaluate effects of a short term improvement of hyperglycemia in diabetic polyneuropathy
Date of disclosure of the study information 2016/04/16
Last modified on 2023/04/21 17:16:44

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Basic information

Public title

The study to evaluate effects of a short term improvement of hyperglycemia in diabetic polyneuropathy

Acronym

Short term glycemic control and diabetic polyneuropathy

Scientific Title

The study to evaluate effects of a short term improvement of hyperglycemia in diabetic polyneuropathy

Scientific Title:Acronym

Short term glycemic control and diabetic polyneuropathy

Region

Japan


Condition

Condition

Diabetic Polyneuropathy

Classification by specialty

Medicine in general Endocrinology and Metabolism Neurology
Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the influences of acute lowering of blood glucose to diabetic polyneuropathy

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

1. Change from screening in corneal confocal microscopic findings at week 2 and month 36

2. Change from screening in nerve conduction studies at week 2 and month 36

Key secondary outcomes

Changes from screeining in tests as below at week 2 and month 36
1. Score of Michigan Neuropathy Screening Instrument(MNSI)
2. Clinical findings: i) Absent or hypoactive Achilles tendon reflexes, ii) Impaired vibration sensation
3. HbA1c, blood glucose
4. Coefficients of variance of RR intervals
5. Diabetic nephropathy, Diabetic retinopathy
6. Laboratory data, blood pressure
7. Safety
8. Current potential threshold
9. Iriscorder
10. Elctroretinography


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

20 years-old <=

Age-upper limit

75 years-old >=

Gender

Male and Female

Key inclusion criteria

Correspond to all of the following in recruitment of participants with type 2 diabetes:
1. Patients whose hospitalization periods are expected more than two weeks.
2. Patients who meets more than 2 of 3 below:
i) Bilateral neuropathic symptom of lower extremities
ii) Bilateral decreased vibration sensation of lower extremities
iii) Bilateral decrease or absence of Achilles tendon reflexes.
3. HbA1c >= 8.0%

Key exclusion criteria

1. Pregnancy, lactation
2. Severe infection, Severe injuries
3. Treatment with steroids
4. Current/Past malignancy
5. Allergic to anesthetic drugs
6. Inappropriate patients for entry on this study in the judgement of the investigator

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Jiro
Middle name
Last name Nakamura

Organization

Aichi Medical University

Division name

Diabetes

Zip code

480-1195

Address

1-1 Yazakokarimata, Nagakute, Aichi 480-1195

TEL

0561-63-1683

Email

jiro@aichi-med-u.ac.jp


Public contact

Name of contact person

1st name Hideki
Middle name
Last name Kamiya

Organization

Aichi Medical University

Division name

Diabetes

Zip code

480-1195

Address

1-1 Yazakokarimata, Nagakute, Aichi 480-1195

TEL

0561-63-1683

Homepage URL


Email

hkamiya@aichi-med-u.ac.jp


Sponsor or person

Institute

Aichi Medical University

Institute

Department

Personal name



Funding Source

Organization

Division of Diabetes, Department of Internal Medicine, Aichi Medical University

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

Aichi Medical University School of Medicine

Address

1-1 Yazakokarimata, Nagakute, Aichi 480-1195

Tel

0561-63-1683

Email

thimeno@aichi-med-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

2016 Year 04 Month 16 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

Enrolling by invitation

Date of protocol fixation

2015 Year 11 Month 20 Day

Date of IRB

2015 Year 11 Month 20 Day

Anticipated trial start date

2015 Year 12 Month 01 Day

Last follow-up date

2026 Year 11 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

1. Longitudinal study without a control group
2. Cases are selected from inpatients of Aichi Medical University


Management information

Registered date

2016 Year 04 Month 15 Day

Last modified on

2023 Year 04 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022971


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name