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Completed

NCT Number: NCT02238795

Sepsis-Associated Purpura Fulminans International Registry - Europe

Sepsis-associated Purpura fulminans (SAPF) is a rare life-threatening condition. It is characterized by multiple skin lesions which rapidly progress to necrosis and gangrene. SAPF is a manifestation of widespread clot formation in small blood vessels which emerges secondarily to severe bacterial and viral infections. The clinical presentation of SAPF is dominated by symptoms of severe sepsis and multiple organ failure which are further aggravated by the massive skin lesions.

At present, there are no evidence-based guidelines for the medical management of SAPF. With numerous therapeutic approaches in use, there are no consistent comparisons of their efficacy. Altered role of causal pathogens following the introduction of meningococcal and pneumococcal prophylactic vaccines also remains to be investigated.

The goal of the registry is comprehensive collection and evaluation of information concerning the epidemiology, morbidity, therapy and outcome of SAPF.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Jena, Klinik für Anästhesiologie und Intensivmedizin, Jena, Germany

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About this study

Purpura fulminans is the clinical manifestation of disseminated thrombosis in dermal and systemic microcirculation. This rare disease is frequently associated with multiple organ failure and represents a life-threatening condition with mortality exceeding 50 %. In the vast proportion of cases, the condition has been shown to emerge secondary to acquired Protein C deficiency associated with severe sepsis, mostly of meningococcal or pneumococcal origin.

A consistent therapeutic approach to sepsis-associated Purpura fulminans (SAPF) has not been established yet. With exaggerated pro-coagulant activity being confirmed as the key pathogenic aspect, several treatment modalities aiming at the balance restoration in the coagulation cascade have been considered.

SAPF causality might have been substantially altered in the wake of widespread meningococcal and pneumococcal vaccination. There are neither evidence-based treatment guidelines nor comparative evaluation of the efficacy of different therapeutic approaches.

The present registry aims at a) large-scale data accumulation and comprehensive evaluation of the incidence, causality and current treatment strategies of SAPF, b) comparative assessment of treatment strategies including or not including protein C supplementation c) identification of patient subgroups of particular eligibility for Protein C treatment, as judged by established criteria of disease severity assessment, d) feedback of aggregated data to registry contributors, thus permitting quality management and standard updates, e) dissemination of data evaluation summaries and recommendations for the use of Protein C formulations in clinical routine, f) elaboration of a framework for SAPF treatment recommendations and guidelines.

The registry comprises prospective, multicentric open-label data collection on the current state of incidence and management of SAPF, regardless of the etiopathogenic background. It will include comprehensive records on diagnosis, morbidity and management of SAPF, supplied in the form of electronic case report forms (eCRFs) by the participating centers over a period of three years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of sepsis and Purpura fulminans
  • Signed informed consent

Exclusion criteria

  • Premature neonates (below gestational age of 36 weeks)

Treatment and study plan

Primary outcomes

  1. Mortality

    Time frame: during hospital stay (estimated up to 3 months)

    All-cause in-hospital mortality

Secondary outcomes

  1. Hospital Stay

    Time frame: duration of hospital stay, up to 3 months

    Hospital stay (in days), patients were observed through hospital stay as long as it took

  2. Extent and Severity of Purpura Fulminans Lesions

    Time frame: 7 days

    Extent and severity of Purpura fulminans lesions: Number of lesions with purpura fulminans

  3. Mean Total Sepsis-related Organ Failure Assessment (SOFA) Score

    Time frame: day 7

    Mean total Sepsis-related organ failure assessment (SOFA) score at day 7, range 0-24 points, higher scores are worse.

    The total SOFA score is the sum of the subscores of central nervous system, cardiovascular system, respiratory system, coagulation, liver and renal function. The range of all subscores is from 0 to 4, with 4 points indicating the worst outcome.

  4. Protein C

    Time frame: until day 7

    Administration of Protein C

  5. Duration of ICU Stay

    Time frame: during ICU stay (estimated up to 3 months)

    Duration of hospitalization in an ICU

  6. Adverse Drug Reactions: Visual Nerve Damage

    Time frame: during hospital stay (estimated up to 3 months)

    Adverse Drug Reaction related to specific PF treatment: Visual nerve damage

  7. Adverse Drug Reaction: Bleeding

    Time frame: during ICU stay

    Occurence of Bleeding (Adverse drug reaction)

  8. Adverse Drug Reaction: Thrombotic Events

    Time frame: during ICU stay

    Occurence of thrombotic events (Adverse Drug Reaction)

  9. Amputation

    Time frame: during ICU stay

    Need for amputation

Other outcomes

  1. Vasopressor Days

    Time frame: during ICU stay (estimated up to 3 months)

    Vasopressor-free days

  2. Ventilator-free Days

    Time frame: during ICU stay (estimated up to 3 months)

    Number of ventilator-free days

  3. Renal Replacement Therapy

    Time frame: during ICU stay (estimated up to 3 months)

    Duration (hours) of renal replacement therapy

Sponsors and collaborators

Lead sponsor

Jena University Hospital

Other

Collaborators

  • Evangelisches Krankenhaus Bielefeld gGmbH
  • Hannover Medical School
  • Insel Gruppe AG, University Hospital Bern
  • Ludwig-Maximilians - University of Munich
  • Medical University of Vienna
  • University Hospital Tuebingen
  • University Hospital of Cologne
  • University Hospital, Basel, Switzerland
  • University Hospital, Essen
  • Universitätsklinikum Hamburg-Eppendorf

Registry information

Acronym: SAPFIRE

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Sep 12, 2014
Registry last updated
May 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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