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Purpura, Schoenlein-Henoch clinical trials

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NCT ID: NCT04655378 Completed - Pediatric ALL Clinical Trials

Validation of the IgA1 Detection Method With Gradient Glycosylation by Mass Spectrometry as a Potential Marker of Renal Involvement in Pediatric Rheumatoid Purpura

FOXIGA-2020
Start date: October 22, 2020
Phase:
Study type: Observational

In this ancillary study on the FoxTreg cohort, the study investigators will select variables to input and thus develop two models (Linear Discriminant Analysis and Decision Tree). The aim of this study is to validate the method in terms of repeatability, reproducibility, control of pre-analytical conditions and sample conservation, to complete the screening of IgA glycosylation in individuals of the FoxTreg cohort and to refine the glycopeptide signature to predict renal involvement.

NCT ID: NCT04387942 Completed - Clinical trials for Purpura, Schoenlein-Henoch

The Therapeutic Value and Mechanism of Recombinant Human Interleukin-2 in Children With Henoch-schönlein Purpura

HSP
Start date: June 14, 2020
Phase: N/A
Study type: Interventional

The study aims to explore the therapeutic value and mechanism of Interleukin-2 on children with Henoch-schönlein purpura.

NCT ID: NCT03410290 Completed - Clinical trials for Giant Cell Arteritis

Journey of Patients With Vasculitis From First Symptom to Diagnosis

Start date: January 11, 2018
Phase:
Study type: Observational [Patient Registry]

This study seeks to understand the journey that patients eventually are diagnosed with vasculitis experience in the period prior to their formal diagnosis by a healthcare provider. Data elements of interest include average time from the onset of the first symptoms to the time a diagnosis of vasculitis is confirmed. Other aims include identifying factors associated with the time to diagnosis. These factors will be divided into: a) intrinsic factors, or so-called "patient-related factors", such as the type of vasculitis symptoms, patient demographics, socioeconomic status, patients' beliefs regarding the etiology of their symptoms, and other factors, and b) extrinsic factors, or "professional/health system factors", such as healthcare access, referral patterns, testing patterns, and other factors. Understanding such factors can guide future efforts to shorten delays in diagnosis and thereby improve outcomes. All analyses will be done for the population of patients with vasculitis as a whole and by individual types of vasculitis.

NCT ID: NCT03222687 Completed - Clinical trials for Henoch-Schönlein Purpura Nephritis

Tacrolimus in Children With Henoch-Schönlein Purpura Nephritis

Start date: September 1, 2015
Phase: Phase 4
Study type: Interventional

Henoch-Schönlein purpura (HSP) is the most common vasculitis in children, with an incidence of approximately 10:100 000 children and a slight male predominance (male-to-female ratio of 1.5:1). Henoch-Schönlein purpura nephritis (HSPN) is the principal cause of morbidity for HSP and 1%-7% of HSPN patients may progress to renal failure or end-stage renal disease. Immunosuppressive therapy has become the standard treatment in children with HSPN, however the use of these drugs are still mainly in an off-label manner in clinical practice. Tacrolimus, a calcineurin inhibitor, has been recently suggested in the treatment of HSPN in children. However, the evidence-based clinical data are still limited. Given the potential benefits and unmet need in clinical practice, the purposes of this pilot study were to assess effectiveness and safety of tacrolimus in HSPN children and evaluate the potential impact of CYP3A5.

NCT ID: NCT02476292 Completed - Vasculitis Clinical Trials

Impact of Vasculitis on Employment and Income

Start date: June 2015
Phase: N/A
Study type: Observational

The purpose of this study is to learn about the impact of vasculitis on employment and income in patients with different systemic vasculitides. All patients enrolled in the Vasculitis Clinical Research Consortium (VCRC) Patient Contact Registry, living in USA or Canada, and followed for more than 1 year since the vasculitis diagnosis will be invited via email to participate in this study, based on an online survey.

NCT ID: NCT02317133 Completed - Clinical trials for Henoch Schönlein Purpura

Study of the Role of Regulator T Cells in the Pathophysiology of Childhood Henoch Schönlein Purpura

FOX-TREG
Start date: February 2015
Phase:
Study type: Observational

The primary objective of this study is to search for evidence of quantitative or functional defects in plasma regulatory T cells (Tregs) in pediatric patients with Henoch Schönlein Purpura (HSP) as compared to a control population.

NCT ID: NCT02190929 Completed - Clinical trials for Giant Cell Arteritis

Educational Needs of Patients With Systemic Vasculitis

Start date: March 2012
Phase: N/A
Study type: Observational [Patient Registry]

A cross-sectional study design and online questionnaire was used to assess the informational needs of patients with several different types of systemic vasculitis. Patients were recruited from within the Vasculitis Clinical Research Consortium (VCRC) online Patient Contact Registry1. Survey responses from participants in the VCRC Patient Contact Registry were compared to responses from a similar survey recently administered to patients within a United Kingdom (UK) based vasculitis support group (Vasculitis UK).

NCT ID: NCT02190916 Completed - Clinical trials for Giant Cell Arteritis

Vasculitis Illness Perception (VIP) Study

Start date: October 2011
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to learn about how patients with vasculitis think about their illness and to assess to what extent patient perceptions of illness are associated with physical, mental, and social functioning

NCT ID: NCT02176070 Completed - Clinical trials for Giant Cell Arteritis

Reproductive Health in Men and Women With Vasculitis

Start date: February 2011
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to learn about reproductive health, including fertility and pregnancies, in people with vasculitis.

NCT ID: NCT00425724 Completed - Clinical trials for Purpura, Schoenlein-Henoch

HSP-glomerulonephritis Trial: MP vs CyA

Start date: January 2000
Phase: Phase 4
Study type: Interventional

No curative treatment of severe HSP nephritis is known. Apart from corticosteroids, immunosuppressive drugs, such as azathioprine and cyclophosphamide, have been used to treat severe HSP nephritis.Limited patient series treated with these drugs have been described, but there are no reports of controlled trials. Cyclosporine A have been used to treat corticosteroid-resistant or corticosteroid-dependent nephrosis. (11) Cyclosporine A has also been used to treat HSP nephritis, but as far as we know, there are no publications reporting such trials. The aim of the study is to compare MP pulses and cyclosporine A for their efficacy in the treatment of HSP nephritis. The efficacy of the two treatments will be assessed on the basis of the duration of nephrosis/nephritis, the maintenance of renal function and the renal biopsy findings.