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Calciphylaxis clinical trials

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NCT ID: NCT03032835 Recruiting - Clinical trials for Chronic Kidney Diseases

Partners Calciphylaxis Biobank

PCB
Start date: January 2017
Phase:
Study type: Observational [Patient Registry]

Calciphylaxis, a vascular calcification disorder, is a rare and serious disorder characterized by calcification of dermal arterioles. There are significant gaps in the understanding of the pathophysiology and risk factors for calciphylaxis. At present, there is no effective treatment. Uncertain pathobiology, rare incidence and lack of collaborative approach have been some of the major limiting factors towards treating calciphylaxis. The Partners Calciphylaxis Biorepository (PCB) aims to address these gaps within calciphylaxis research by utilizing existing and, when necessary, developing new infrastructure to support the consent of patients and the collection of dedicated samples for a calciphylaxis repository.

NCT ID: NCT02854046 Completed - Calciphylaxis Clinical Trials

Calciphylaxis : Population, Risk Factors, Diagnostic Practice, Therapeutic and Outcome

CalciWest
Start date: July 1, 2016
Phase:
Study type: Observational

Calciphylaxis, also called Calcific Uremic Arteriolopathy (CUA) is a lethal affection mostly affecting patient in end stage renal disease. The survival rate is described around 20 to 46% at one year. Clinical presentation is very painful skin lesions with ulceration mostly located on the trunk or thigh. Current knowledge about physiopathology, diagnostic practice and therapeutic is very limited. Actually there is no European study about calciphylaxis and risk factors, diagnostic practice and outcome factors.

NCT ID: NCT02790073 Completed - Calciphylaxis Clinical Trials

Phase 2 Study With SNF472 in Calciphylaxis Patients

Start date: May 2016
Phase: Phase 2
Study type: Interventional

To evaluate the effect of SNF472 on top of standard of care on promoting wound healing and other parameters of therapeutic response in haemodialysis patients with calciphylaxis (calcific uraemic arteriolopathy, CUA).

NCT ID: NCT02635373 Recruiting - Calciphylaxis Clinical Trials

European Calciphylaxis Registry Network

EuCalNet
Start date: December 2015
Phase: N/A
Study type: Observational [Patient Registry]

Observational, registry, prospective, non-interventional collection of CUA patient data. Patient treatment is carried out within clinical routine, at the discretion of the physicians and according to existing treatment guidelines. Participating physicians will not be subject to any instructions with regard to the diagnosis and therapy of their patients.

NCT ID: NCT02527213 Terminated - Calciphylaxis Clinical Trials

Randomized Double Blind Placebo Controlled Trial of Sodium Thiosulfate for the Treatment of Pain Associated With Calcific Uremic Arteriolopath

Start date: January 30, 2015
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of Sodium Thiosulfate (STS) compared to placebo, in reducing analgesic requirement in subjects with calcific uremic arteriolopathy (CUA) during an initial 28-day treatment phase.

NCT ID: NCT02278692 Completed - Calciphylaxis Clinical Trials

Evaluation of Vitamin K Supplementation for Calcific Uremic Arteriolopathy

VitK-CUA
Start date: March 2015
Phase: N/A
Study type: Interventional

Calcific uremic arteriolopathy a.k.a. calciphylaxis is a vascular calcification disorder seen in dialysis patients. Calcific uremic arteriolopathy has 60-80% one-year mortality and significant morbidity associated with non-healing and extremely painful skin lesions. At present, there is no effective treatment for calcific uremic arteriolopathy. Vitamin K is an important vitamin for inhibiting vascular calcification. It is known to increase the circulating levels of carboxylated Matrix Gla Protein, a potent inhibitor of vascular calcification. However, the effects of vitamin K supplementation in patients with calcific uremic arteriolopathy are unknown. The purpose of this study is to conduct a pilot randomized controlled trial to examine the effects of oral vitamin K supplementation on circulating levels of anti-calcification factor (carboxylated Matrix Gla Protein) and clinical outcomes in patients with calcific uremic arteriolopathy.

NCT ID: NCT01578382 Completed - Calciphylaxis Clinical Trials

Pathophysiology of Martorell Hypertensive Ischemic Leg Ulcer (HYTILU)

Start date: September 2011
Phase:
Study type: Observational

Martorell hypertensive ischemic leg ulcer is a severe type of skin necrosis (skin infarction) which occurs in long-term hypertensive subjects. Calciphylaxis (calcific uremic arteriolopathy) is a severe type of skin necrosis (skin infarction) which occurs in subjects with end-stage kidney disease or after kidney transplantation.

NCT ID: NCT01289626 Completed - Calciphylaxis Clinical Trials

Efficacy of Lanthanum Carbonate in Calciphylaxis

Start date: February 2011
Phase: Phase 1
Study type: Interventional

The research question and primary aim is to determine if lanthanum carbonate is effective in treating calciphylaxis by measurement of complete or partial remission of skin lesions. Secondary endpoints will be measured to determine if lanthanum carbonate can lower calcium-phosphorus product levels, intact PTH and mortality. Albumin levels will be measured as a marker of nutritional status and inflammation.