Acute Kidney Injury (Nontraumatic)

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Review clinical trials related to Acute Kidney Injury (Nontraumatic). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

WISDOM UK: Low Dose-intensity Versus Standard Dose-intensity CRRT in Critically Ill Patients

Acute kidney injury is a potentially life threatening condition which affects 1 in 2 patients in the Intensive Care Unit (ICU). Patients often need dialysis treatment, also called renal replacement therapy. Renal replacement therapy is a treatment that removes toxins and excess fluid from the blood stream. It consists of having a small plastic catheter in a vein in the neck or in the groin through which blood flows through a dialysis machine and is cleansed and excess water is removed. The cleansed blood is then returned to the patient via the same catheter. One of the major areas of uncertainty for doctors in the ICU is "What is the right intensity of renal replacement therapy for patients with acute kidney injury?" A higher intensity indeed removes more toxins but also removes other substances in the blood, including vitamins, nutrients and important medications. The current usual dose is around 25 ml/kg/hr but clinical practice in the UK is very variable and some patients routinely receive higher doses and some get lower doses. Data from large databases worldwide have suggested that a lower dose is safe and effective and may potentially allow the kidneys to recover faster but confirmation is lacking. In this study, the investigators investigate whether renal replacement therapy at a lower intensity is as effective and safe as currently used doses. Participants will be randomised to receiving renal replacement therapy at usual or lower intensity. There will be no change to any other aspects of treatment. The results will inform the investigators whether the study protocol is feasible and how best to design a future larger research study.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Guy's and St Thomas' NHS Foundation TrustUpdated: Mar 5, 2026Locations: 1
Eligibility criteria

age ≥ 18 years [+3]

indication for sustained higher dose-intensity CRRT [+3]

Status: Recruiting

Effect of an Intervention to Prevent Acute Kidney Injury Versus Standard Care in High-risk Patients After Major Surgery

There is no specific therapy for acute kidney injury. It is presumed that supportive measures improve the care and outcome of patients with acute kidney injury. To investigate whether an implementation of a supportive extended care "bundle" in high-risk patients for persistent acute kidney injury (AKI) can reduce the occurrence of persistent surgical AKI. In order to investigate whether the extended KDIGO bundle can prevent persistent AKI in patients with high chemokine ligand 14 (CCL14) as well as in patients with low CCL14, patients will be randomized with stratification by the CCL-value.

Participants needed: 480
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital MuensterUpdated: Aug 1, 2024Locations: 1
Eligibility criteria

Adult patients (age ≥18 years) [+2]

Dialysis-dependent chronic kidney disease [+7]

Status: Recruiting

AKI Risk Factors Analysis After Intentional Hypotensive Anesthesia

This project investigates intentionally hypotensive management such as NTG (nitroglycerin) or NTG+Trandate during general anesthesia in patients undergoing orthognathic surgery. Throughout the entire surgical procedure, blood biochemical and urine monitoring will be conducted. Serum creatinine (Cr) levels, urine analysis, and perioperative monitoring will be utilized as indicators for assessing renal function during the surgery. The objective is to assess its potential renal injury and identify early risk factors for acute kidney injury (AKI). Timely recognition of these factors will allow for the implementation of appropriate intervention strategies, aiding in the prevention of postoperative acute kidney injury. This approach contributes to achieving the goals of Enhanced Recovery After Surgery (ERAS) for surgical patients, promoting faster postoperative recovery.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kaohsiung Medical University Chung-Ho Memorial HospitalUpdated: Feb 14, 2024Locations: 1Duration: 7 Days
Eligibility criteria

America society anesthesiologist classification class I to II patients undergoin... [+1]

patients with arthritis with limited mouth opening [+6]