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Evaluation of efficacy of Kremezin in peripheral arterial disease patients with chronic kidney disease.

Evaluation of efficacy of Kremezin in peripheral arterial disease patients with chronic kidney disease. - Evaluation of efficacy of Kremezin in peripheral arterial disease patients with chronic kidney disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013577
Enrollment
40
Registered
2014-03-31
Start date
2014-04-01
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

Peripheral arterial disease with chronic kidney disease

Interventions

Treatment with Kremezin (6g/day) for 12 month

Sponsors

Shonan Kamakura General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) CKD: CKD stage G3a - G5 2) PAD: Fontaine classification I - II 3) Age 20 - 85 years old at the time of consent to participate in the study 4) Outpatient 5) Patients who have personally and voluntarily provided written informed consent, after having received and thoroughly understood an adequate explanation about participation in the study

Exclusion criteria

Exclusion criteria: 1) Patients with diabetes 2) Patients who have newly taken NSAIDs during this study 3) Patients who have taken iodinated contrast medium or gadolinium contrast medium during entry period 4) Patients with major limb amputation 5) Patients with prior stroke and/or prior coronary artery disease 6) Patients with coronary stent by arteriosclerosis 7) Patients who have gastrointestinal obstruction 8) Patients who in currently pregnant, parturient, breast-feeding, or plan to become pregnant during the study period 9) Patients who are judged unsuitable for this study by the doctor in charge of the patients

Design outcomes

Primary

MeasureTime frame
CAVI(Cardio-ankle vascular index)

Secondary

MeasureTime frame
1) Renal function: 1/sCr, eGFR 2) Marker: IS, FGF-23 3) Vascular function: PDMP, %FMD, ABI, SPP 4) Diagnostic imaging: pACS 5) Insulin resistance: HOMA-R 6) Safety: Adverse effect

Countries

Japan

Contacts

Public ContactTomoko Machida

Mirai Iryo Research Center Inc, Clinical Research Promotion Dept.

machida@mirai-iryo.com03-3263-4801

Outcome results

None listed

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