Shiga Progression of Diabetes, Nephropathy and Retinopathy

NCT00846716 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2009-02-19

No results posted yet for this study

Summary

The purpose of this study is to investigate whether the oral anti-diabetic drug, Thiazolidine (TZD) is effective in suppression of onset or progressin of diabetic nephropathy in Japanese type 2 diabetic patients.

Conditions

Interventions

DRUG

Pioglitazone add on to SU or biguanide

As an initial dosing, 15mg/day of pioglitazone is administered to the patients for 2 years, who are taking SU or biguanide.

DRUG

SU or Biguanide

As an initial dose,a common dose of SU or biguanide is administered to the patients for 2 years.

Sponsors & Collaborators

  • Kanazawa Medical University

    collaborator OTHER
  • Nagahama Red Cross Hospital

    collaborator OTHER
  • Nagahama City Hospital

    collaborator OTHER
  • Kohka Public Hospital

    collaborator UNKNOWN
  • Second Okamoto General Hospital

    collaborator UNKNOWN
  • Omihachiman COmmunity Medical Center

    collaborator UNKNOWN
  • Yasu Hospital

    collaborator UNKNOWN
  • Toyosato Hospital

    collaborator UNKNOWN
  • Ako City Hospital

    collaborator OTHER
  • Horide Clinic

    collaborator UNKNOWN
  • Kawabata Clinic

    collaborator UNKNOWN
  • Seta Clinic

    collaborator UNKNOWN
  • Shiga Clinic

    collaborator UNKNOWN
  • Osaka University

    collaborator OTHER
  • NTT West Osaka Hospital

    collaborator UNKNOWN
  • Hyogo prefectural Amagasaki Hospital

    collaborator UNKNOWN
  • Tomita Clinic

    collaborator UNKNOWN
  • Sawada Clinic

    collaborator UNKNOWN
  • Social Insurance Shiga Hospital

    collaborator UNKNOWN
  • Shiga University

    lead OTHER

Principal Investigators

  • Atsunori Kashiwagi, PhD. · Tsukiwa-machi, Seta, Otsu, Shiga, Japan

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2011-11-30
Completion
2011-11-30

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00846716 on ClinicalTrials.gov