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Comparative Study of Ischemia Techniques in Partial Nephrectomy and Their Effects on Kidney Function

Prospective Controlled Study on the Impact of Ischemia Techniques during Partial Nephrectomy on Postoperative Renal Function

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119792
Enrollment
Unknown
Registered
2026-03-03
Start date
2025-07-21
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Primary malignant tumor of the kidney

Interventions

Zero ischemia group:Zero ischemia
Cold ischemia group:Cold ischemia
Warm ischemia group:Warm ischemia group

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with renal cell carcinoma (RCC) who are highly suspected by pathology or imaging and are scheduled for surgical resection, and meet the clinical diagnostic criteria for locally advanced or high-risk renal cell carcinoma; (YNMT)·; 2.Planned to undergo partial nephrectomy; 3.Complete clinical assessment data are available before the operation, including imaging examinations (such as enhanced CT, MRI, renal dynamic imaging, etc.) and laboratory indicators (such as renal function, tumor markers); 4.Age >=18 years old, gender not limited; 5.There are no other active malignant tumors, and no complications that seriously affect the safety of surgery or adjuvant therapy.

Exclusion criteria

Exclusion criteria: 1.Patients with non-renal cell carcinoma or those with an unclear pathological diagnosis; 2.Previously received systemic targeted therapy, immunotherapy or radiotherapy, and currently in the recurrence or extensive metastasis stage; 3.It is complicated with severe cardiopulmonary insufficiency, liver and kidney failure, active infection, etc., and cannot tolerate surgery or adjuvant therapy; 4.Combined with severe mental illness, cognitive impairment or other conditions that affect research compliance; 5.Unable to cooperate with postoperative follow-up or expected to be unable to complete relevant evaluations and data collection during the study period; 6.Currently participating in other interventional clinical studies that may interfere with the evaluation of this study.

Design outcomes

Primary

MeasureTime frame
Change in estimated Glomerular Filtration Rate;Recurrence-Free Survival (RFS);;Overall Survival (OS);

Secondary

MeasureTime frame
Intraoperative blood loss;Ischemia duration;Chronic kidney disease stage change;Perioperative complications;Incidence of AKI;

Countries

China

Contacts

Public ContactQi Zhang

Zhejiang Provincial People's Hospital

clinic@126.com+86 138 5801 9285

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026