Hemolytic Uremic Syndrome

3

Review clinical trials related to Hemolytic Uremic Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Hyperhydration in Children With Shiga Toxin-Producing E. Coli Infection

The objective of this study is to determine if early high volume intravenous fluid administration (hyperhydration) may be effective in mitigating or preventing complications of shiga toxin-producing E. coli (STEC) infection in children and adolescents when compared with traditional approaches (conservative fluid management).

Participants needed: 1,040
Trial details
Age: 9-21Biological sex: AllType: InterventionalSponsor: University of CalgaryUpdated: May 18, 2026Locations: 26
Eligibility criteria

Aged 9.0 months to <21 years at the time of informed consent. [+8]

Hematocrit <30% AND [+11]

Status: Recruiting

Efficacy of INM004 in Children With STEC-HUS

The objectives of this study are to evaluate the efficacy, safety, and pharmacokinetics of INM004 in pediatric patients with Hemolytic Uremic Syndrome associated to infection by Shiga toxin-producing Escherichia coli (STEC-HUS).

Participants needed: 220
Trial details
Phase: Phase 3Age: 9-17Biological sex: AllType: InterventionalSponsor: Inmunova S.A.Updated: Jan 15, 2026Locations: 52
Eligibility criteria

Age ≥ 9 months and < 18 years at the time of randomization. [+13]

Start of dialysis within 48 hours prior to admission to the participating instit... [+16]

Status: Recruiting

Complement Prospective Evaluation of Thrombotic Microangiopathy on Endothelium

Thrombotic microangiopathy (TMA) is a severe and life-threatening condition, often affecting the kidneys and brain. It can occur on the background of various clinical conditions. Dysregulation of the alternative pathway of complement may be the etiological factor and this type of TMA is classified, according to the current nomenclature, as primary atypical hemolytic uremic syndrome (HUS). Half the patients with primary atypical HUS present with rare variants in complement genes, although coexisting conditions are often needed for the TMA to become manifest. In patients with secondary atypical HUS, certain coexisting conditions appear to drive the disease and treatment should target the underlying condition to remit the TMA. Recently, the investigators demonstrated, by using a novel in-house developed functional endothelial cell-based test, that complement dysregulation and overactivation is the dominant cause of disease and its sequelae in a subset of patients with secondary atypical HUS, having impact on treatment and prognosis. The investigators did first prove this concept in patients presenting with TMA and hypertensive emergency. A prospective study is needed to further corroborate these findings along the spectrum of TMA. The investigators hypothesize that their functional endothelial cell-based test, the so-called "HMEC" test, can better categorizes the TMA into different groups with potential therapeutic and prognostic implications. Thus, paving the road to the ultimate goal of precision medicine.

Participants needed: 42
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Maastricht University Medical CenterUpdated: Oct 1, 2025Locations: 1Duration: 12 Months
Eligibility criteria

Males or females at least 18 years of age; [+7]

Have secondary causes of hypertensive emergency, including renovascular hyperten... [+8]