Calcific Uremic Arteriolopathy, Calciphylaxis
Conditions
Brief summary
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.
Detailed description
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.
Interventions
DRUGSodium thiosulfate
Additional treatment(s) due to lesion progression When intervention occurs, the date of the intervening event should be recorded in the source documents and the (CRF). The subject should continue in the study as scheduled.
DRUGPlacebo
Additional treatment(s) due to lesion progression When intervention occurs, the date of the intervening event should be recorded in the source documents and the (CRF). The subject should continue in the study as scheduled.
Sponsors
American Regent, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Males or females ≥18 years of age who are able to give informed consent. 2. Calcific uremic arteriolopathy (CUA), either newly-diagnosed or pre-existing, currently on STS or not yet treated with STS and either not on pain medication or on a stable pain medication regimen. The diagnosis of calciphylaxis can be made when: * The following clinical features are all present, or two (2) of the following clinical features and typical histopathological findings are present. Clinical features: 1. A patient on chronic hemodialysis for chronic kidney disease or with a glomerular filtration rate (GFR) of less than 15/ml/min/1.73 m2 2. More than 2 painful and non-treatable skin ulcers with concomitant painful purpura 3. Painful and non-treatable skin ulcers on the trunk, extremities, or penis with concomitant painful purpura Histopathological findings by skin biopsy when 3 clinical findings are not present: 1. Necrosis and ulceration of the skin with calcification of the tunica media and internal elastic membrane of small to medium-sized arterioles of dermis and subcutaneous fat are essential for the diagnosis 2. Concentric stenosis due to edematous intimal thickening is also seen in the small to medium-sized arterioles of dermis and subcutaneous fat 3. End stage renal disease (ESRD) on chronic maintenance hemodialysis. 4. Willingness to undergo washout of pre-existing STS treatment (if required by treatment allocation) and to continue in a double blind treatment period of 4 weeks, during which they might receive placebo. 5. Ability to comply with all study requirements.
Exclusion criteria
1. History of allergic or other adverse reaction to STS 2. Current treatment with STS for indications other than CUA (e.g. cyanide poisoning) 3. Currently on alternative treatment for CUA as listed below. Unless treatment has been discontinued for at least 1 month prior to the screening visit. 1. Steroids 2. Hyperbaric Oxygen 3. Bisphosphonates 4. Pentoxifylline 5. Tissue Plasminogen Activator 6. Lucilia sericata larvae (maggot therapy) 7. On Cinacalcet for treatment for CUA (i.e. cinacalcet was either started or dose increased after the appearance of lesions) 4. Any co-existing disease or problem that makes participation in the study unadvisable for the patient or compromises integrity of the study 1. Cirrhosis of the liver 2. History of congestive heart failure (New York Heart Association class III or IV) with multiple hospital admissions (at least 3 admissions in 6 months) 3. Persistent and uncontrolled metabolic acidosis 5. Chronic kidney disease or renal transplant patients with diagnosis of calciphylaxis who are not on hemodialysis. 6. Any other disease or condition which, in the judgment of the Investigator, would place a subject at undue risk by being enrolled in the trial, or cause inability to comply with the trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Reduction in Analgesic Requirement | up to 28 Days | The length of time in days, from first treatment with blinded study drug; to when subject requires rescue analgesic |
Countries
United States
Outcome results
None listed