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The measurement of predictors on acute kidney injury in patients with robot-assisted partial nephrectomy

The measurement of predictors on acute kidney injury in patients with robot-assisted partial nephrectomy - The measurement of predictors on acute kidney injury in patients with robot-assisted partial nephrectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051201
Enrollment
20
Registered
2023-05-30
Start date
2019-08-20
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

Renal cell carcinoma

Interventions

from August 2019 to March 2020

Sponsors

Department of Urology, Kurume University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Clinically diagnosed as cT1 (including some cT1b) renal cancer by abdominal contrast-enhanced CT (or MRI examination for patients in whom contrast agents are not applicable), and partial nephrectomy is possible 2) No lymph node and metastasis to other intra-abdominal organs (cN0, cM0) by abdominal contrast-enhanced CT (MRI examination for patients who cannot adapt to contrast agents) 3) Chest CT and bone scintigraphy show no metastasis (cM0) 4) Single tumor 5) The latest test values within 6 weeks (42 days) before registration meet all of the criteria for the following items (WBC, Platelet, AST, ALT, T-Bil, Serum creatinine) 6) Aged 20 years or older at the time of informed consent 7) Written consent has been obtained from the patient to participate in the study

Exclusion criteria

Exclusion criteria: 1) Active double cancer 2) History of renal transplantation in the past 3) Receiving treatment for renal cancer within 6 months 4) Inability to discontinue anticoagulants 5) Anemia requiring blood transfusion or bleeding tendency 6) Patients with morbid obesity (BMI 35 over) 7) Patients undergoing dialysis 8) Pregnant women, women who may be pregnant, or women who are breastfeeding 9) Complications of psychiatric disease or psychiatric symptoms and judged to be difficult to participate in the study 10) Other reasons - the principal investigator or subinvestigator of the medical institution participating in this study determines that the participant is ineligible to participate in this study

Design outcomes

Primary

MeasureTime frame
urine and blood biomarker for acute renal injury (L-FABP, NGAL, KIM-1)

Countries

Japan

Contacts

Public ContactMitsunori Matsuo

Kurume University School of Medicine Department of Urology

mmatsuo@med.kurume-u.ac.jp0942-31-7572

Outcome results

None listed

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