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A prospective observational cohort study on the renal injury related to non-cardiac surgery in different types of anemia

A prospective observational cohort study on the renal injury related to non-cardiac surgery in different types of anemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111959
Enrollment
Unknown
Registered
2025-11-07
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Kidney injury

Interventions

Sponsors

The First Affiliated Hospital of Wannan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2.Scheduled elective non-cardiac, non-intracranial surgery, with an expected duration of surgery > 1 hour and a post-operative hospital stay > 24 hours; 3. The subject or their family member can understand the study protocol and is willing to participate in this study, providing written informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnancy status; 2.Long-term living at altitudes above 2500 meters, or recent residence in areas above 2500 meters for more than 3 months; 3. Suffering from blood system diseases other than anemia; 4.Presence of serious comorbidities that may interfere with outcome indicators, such as uremia or neurological disorders; 5.Unable to cooperate or unable to understand the conditions and objectives of this study, or refusing to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Incidence of kidney injury;

Secondary

MeasureTime frame
The difference in the incidence of perioperative acute kidney injury between patients with preoperative anemia and non-anemic patients.;Allogeneic blood transfusion;Hospitalization time;Second hospitalization;Severe complications at different time points after surgery (Clavien-Dindo grade III and above complications) and mortality.;Incidence of adverse events (e.g., nausea and vomiting, pulmonary infection, cough with sputum, thrombosis, etc.);

Countries

China

Contacts

Public ContactChen Yongquan, Lu Meijing

The First Affiliated Hospital of Wannan Medical College

619466076@qq.com+86 139 5536 7332

Outcome results

None listed

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