Retrospective Study Evaluating the Contribution of Rheopheresis in the Treatment of Uremic Calciphylaxis (RHEO-CUA)

Sponsor
Association ECHO (Other)
Overall Status
Recruiting
CT.gov ID
NCT05633121
Collaborator
European Clinical Trial Experts Network (Other), Elsan (Other)
55
1
28.4
1.9

Study Details

Study Description

Brief Summary

Calcifying uremic arteriolopathy (or uremic calciphylaxis) is a rare disease (prevalence <1% of dialysis patients), but the prognosis is often catastrophic. The main non-modifiable risk factors are age, female gender, diabetes, obesity and length of time on dialysis. Today, there is no specific treatment for this pathology, and the therapeutic management is poorly codified. However, it is commonly accepted that the treatment is based on the control of risk factors, local care, and the possible addition of treatment with sodium thiosulfate. Hyperbaric oxygen therapy has also been proposed by some authors, but remains not very accessible in practice.

Recently, it has been proposed to use Rheopheresis as an adjuvant treatment for severe forms of uraemic calciphylaxis. It is a technique of apheresis in double filtration, allowing the extraction of molecules of high molecular weight, and thus the improvement of the rheological conditions of microcirculation. The expected effect is the improvement of tissue oxygenation and the acceleration of the healing of skin lesions, with the consequent reduction of infectious complications.

The aim of this study is to propose a large national retrospective study, studying the evolution of patients with uremic calciphylaxis and treated by rheopheresis, compared to a control group. This will allow to have a more precise idea of the contribution of Rheopheresis in this indication.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Rheopheresis

Study Design

Study Type:
Observational
Anticipated Enrollment :
55 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Retrospective Study Evaluating the Contribution of Rheopheresis in the Treatment of Uremic Calciphylaxis
Actual Study Start Date :
May 20, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Sep 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Patient suffering from uremic calciphylaxis treated with rheopheresis

Procedure: Rheopheresis
Technique of apheresis in double filtration, allowing the extraction of molecules of high molecular weight, and thus the improvement of the rheological conditions of microcirculation. The expected effect is the improvement of tissue oxygenation and the acceleration of the healing of skin lesions, with the consequent reduction of infectious complications.

Patient suffering from uremic calciphylaxis not treated with rheopheresis

Outcome Measures

Primary Outcome Measures

  1. Proportion of patients fully recovered 6 months after diagnosis. [6 months]

    Complete healing will be defined by the healing of all skin lesions without the appearance of new ones.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patient

  • Chronic hemodialysis

  • Uraemic calciphylaxis (clinical or histological diagnosis) diagnosed between January 2010 and December 2022,

  • Rheopheresis treatment initiated within one month of calciphylaxis diagnosis (for the exposed group)

  • Patient informed and not opposed to the use of their health data.

Exclusion Criteria:
  • minor patient,

  • Advanced cognitive disorders.

Contacts and Locations

Locations

Site City State Country Postal Code
1 ECHO - Pole Santé Sud Le Mans France 72000

Sponsors and Collaborators

  • Association ECHO
  • European Clinical Trial Experts Network
  • Elsan

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Association ECHO
ClinicalTrials.gov Identifier:
NCT05633121
Other Study ID Numbers:
  • RHEO-CUA
First Posted:
Dec 1, 2022
Last Update Posted:
Dec 12, 2022
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 12, 2022