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Risk Factors and Prediction Model Establishment for Acute Kidney Injury Following Transcatheter Aortic Valve Implantation

Risk Factors and Prediction Model Establishment for Acute Kidney Injury Following Transcatheter Aortic Valve Implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110257
Enrollment
Unknown
Registered
2025-10-11
Start date
2025-10-31
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Aortic Stenosis

Interventions

Case group:none

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age requirements: adult patients over 18 years old. 2. Diagnosis of moderate to severe aortic valve disease: Diagnosis of moderate to severe aortic valve disease based on echocardiography. 3. Undergo medical surgery: All patients undergo transcatheter aortic valve replacement. 4. Postoperative biochemical test available: At least one postoperative biochemical test data is available, and the data is complete. 5. Complete basic data: Comprehensive clinical and surgical data, including demographic characteristics, intraoperative and postoperative monitoring indicators, etc.

Exclusion criteria

Exclusion criteria: 1. Previous history of kidney disease: There is a history of chronic nephritis and renal insufficiency. 2. Serious underlying diseases: Combined with end-stage liver disease, renal insufficiency (especially in patients requiring dialysis), malignant tumors and other serious diseases. 3. Major perioperative complications: Such as severe perioperative infection or sepsis, which may significantly affect creatinine levels and interfere with study results. 4. Missing data: Patients with incomplete postoperative biochemical test data or other missing key clinical data. 5. Pregnant patients: Pregnant patients are excluded due to physiological differences and special circumstances. 6. Insufficient follow-up: The postoperative follow-up time is short or the patient dies from other reasons after surgery, and relevant data cannot be fully collected.

Design outcomes

Primary

MeasureTime frame
Hyperlactatemia is present;

Countries

Ching

Contacts

Public ContactZhang Xiaodan

Nanjing First Hospital

1174300725@qq.com+86 158 9595 0788

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026