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Effect of Pioglitazone on Serum FGF-23 Levels in Patients with Diabetic Kidney Disease: A Randomized Controlled Trial

Effect of Pioglitazone on Serum FGF-23 Levels in Patients with Diabetic Kidney Disease: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210316009
Enrollment
40
Registered
2021-03-16
Start date
2020-08-17
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

T2DM CKD stage 3-4 patients T2DM CKD stage 3-4 patients

Interventions

oral 15mg per day pioglitazone,standard treatment
Experimental Drug,No Intervention No treatment
Pioglitazone group,Control group

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age of 18 years or more 2. T2DM with stable HbA1c 6-8% 3. eGFR 15-59 ml/min/1.73m2 with stable renal function in 12 weeks 4. Stable calcium and phosphate level

Exclusion criteria

Exclusion criteria: 1. history of AKI in 12 weeks 2. History of heart failure or volume overload within 12 weeks 3. History of frequent hypoglycemia 4. History of fracture or bladder cancer 5. Previous pioglitazone and insulin use 6. Previous side effects of pioglitazone

Design outcomes

Primary

MeasureTime frame
reduction of serum intact FGF-23 at 16 weeks after end of intervention laboratory test

Secondary

MeasureTime frame
changes of serum calcium, phosphate, intact PTH, HbA1c and HOMA-IR 16 weeks laboratory test

Countries

Thailand

Contacts

Public ContactWutipong Triwatana

Department of internal medicine, Phramongkutklao hospital

wutipong.tri@pccms.ac.th0874966685

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026