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Multicenter clinical trial of pioitazone in type 2 diabetes: impact on expression of soluble receptor for advanced glycation end-products (PioRAGE)

Multicenter clinical trial of pioitazone in type 2 diabetes: impact on expression of soluble receptor for advanced glycation end-products (PioRAGE) - Effect of pioglitazone on circulating soluble receptor for advanced glycation end-products (PioRAGE)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002055
Enrollment
100
Registered
2009-06-09
Start date
2009-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

type 2 diabetes

Interventions

pioglitazone 15-30 mg/day glimepiride 1-4 mg/day

Sponsors

PioRAGE research group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)subjects who had a baseline glycated hemoglobin(HbA1C) level of 6.0 % or more and below 10.0 % 2)subjects who agreed to participate with written informed concent

Exclusion criteria

Exclusion criteria: 1)subjects currently on pioglitazone therapy 2)subjects under treatment with insulin 3)subjects under treatment with glimepiride 3-6 mg/day or gliclazide 80-160 mg/day or glibenclamide 5-10 mg/day 4)subjects with congestive heart failure 5)subjects with liver cirrhosis 6)subjects with renal dysfunction (serum creatinine level is 2.0 mg/dl or more) 7)subjects with malignant diseases or hard to be followed 8)subjects who were judged to be inappropriate for inclusion

Design outcomes

Primary

MeasureTime frame
serum soluble form of receptor for advanced glycation end-products(sRAGE), serum endogenous secretory RAGE(esRAGE)

Secondary

MeasureTime frame
1)surface RAGE expression on isolated peripheral blood mononuclear cells (PBMCs) 2)serum adiponectin, serum fetuin A, serum TNF-related apoptosis-inducing ligand(TRAIL), serum osteoprotegerin(OPG), serum high sensitivity C-reactive protein(hs-CRP) 3)gene expression of PBMCs(RAGE, ADAM10, ADAM17) 4)serum carboxymethyllysine(CML)

Countries

Japan

Contacts

Public ContactShinji Tanaka

Osaka City University Graduate School of Medicine Department of Metabolism, Endocrinology and Molecular Medicine

stana@med.osaka-cu.ac.jp06-6645-3806

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026