Patient Registry Study of Berinert® in Normal Clinical Practice
| Status: | Completed |
|---|---|
| Conditions: | Skin and Soft Tissue Infections |
| Therapuetic Areas: | Dermatology / Plastic Surgery |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 3/1/2014 |
| Start Date: | April 2010 |
| End Date: | April 2014 |
| Contact: | Clinical Trial Registration Coordinator |
| Email: | clinicaltrials@cslbehring.com |
Patient Registry for Berinert®, a C1-Esterase Inhibitor
The objective of this patient registry is to collect data on the safety of Berinert® in
normal clinical practice in the United States. The patient registry will be maintained for a
period of at least 3 years. The duration of individual patient participation will vary and
is determined by the frequency of hereditary angioedema (HAE) attacks and the patient's need
for Berinert® treatment.
normal clinical practice in the United States. The patient registry will be maintained for a
period of at least 3 years. The duration of individual patient participation will vary and
is determined by the frequency of hereditary angioedema (HAE) attacks and the patient's need
for Berinert® treatment.
Inclusion Criteria:
- Any patient receiving CSL Behring's C1-esterase inhibitor
- Written informed consent (may not be required for some retrospective chart review
cases)
Exclusion Criteria:
- Any patient participating in an HAE study using other C1-inhibitors than Berinert®
We found this trial at
32
sites
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