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Study on the Safety of Easing Bed Rest Restrictions After Kidney Biopsy

A Prospective Case Series Study on the Safety of Easing Bed Rest Restrictions After Percutaneous Kidney Biopsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1040240010
Enrollment
179
Registered
2024-04-08
Start date
2024-04-11
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

Kidney diseases

Interventions

Alleviation of the post-renal biopsy rest requirements compared to the methods previously practiced at our institution

Sponsors

Iwakura Takamasa
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria 1. Patients who are 18 years of age or older and are independent in activities of daily living, and undergo percutaneous renal biopsy in the Department of Nephrology of our hospital. 2. Patients with preserved renal function (eGFR > 30 mL/min/1.73m2). 3. Patients whose blood pressure on the day of renal biopsy is managed to be less than 160/100 mmHg. 4. Patients for whom multiple nephrologists, including the principal investigator (Takamasa Iwakura), a specialist in nephrology, have determined a low risk of complications based on renal morphology depicted by ultrasound. 5. Patients for whom consent has been obtained by signing the informed consent form for participation in this study.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria will not be included in this study: 1. Patients who show coagulation abnormalities (prothrombin time, activated partial thromboplastin time prolongation) or thrombocytopenia (platelet count < 100,000/uL) on admission tests. 2. Patients who show anemia (hemoglobin < 10 g/dL) on admission tests. 3. Patients suspected of renal amyloidosis based on clinical course and blood/urine tests. 4. Patients with difficult blood pressure control in the post-renal biopsy course. 5. Patients who show a hematoma of 40 mL or more on ultrasound examination at the end of renal biopsy. 6. Patients who show a significant increase in hematoma size on ultrasound examination 1 hour after renal biopsy. 7. Patients who show bleeding symptoms (intractable back or abdominal pain, unstable vital signs) within 4 hours after renal biopsy. 8. Patients with gross hematuria.

Design outcomes

Primary

MeasureTime frame
The proportion of patients who underwent transfusion or endovascular treatment due to bleeding complications after relaxation of post-renal biopsy rest within 4 hours

Secondary

MeasureTime frame
1.The proportion of patients who exhibited bleeding symptoms (intractable back or abdominal pain, unstable vital signs) after relaxation of post-renal biopsy rest. 2. The proportion of patients who developed gross hematuria after relaxation of post-renal biopsy rest. 3. The proportion of patients who required extended hospitalization due to complications.

Contacts

Public ContactTakamasa Iwakura

Hamamatsu University school of Medicine

tkms0421@hama-med.ac.jp+81-534352261

Outcome results

None listed

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