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Retrospective Evaluation of CroFab - Efficacy in Severe Envenomation

Sponsored by BTG International Inc.

About this trial

Last updated 3 years ago

Study ID

MC03/03/05

Status

Completed

Type

Observational

Placebo

No

Accepting

18-75 Years
All
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 20 years ago

What is this trial about?

Retrospective observational review of severe envenomation treatment with CroFab

What are the participation requirements?

Yes

Inclusion Criteria

- Must involve treatment of a human patient with CroFab between January 1, 2002 and December 31, 2004 - The record must contain all of the following: 1. Clinical signs/symptoms prior to the first dose of antivenom, 2. Documentation of all doses of antivenom used to treat the patient, 3. Indication of whether or not initial control was achieved with antivenom. To be included in the Efficacy Evaluable Population (EEP) in the current analysis, each record must meet the following criteria: - Must contain enough information to calculate a severity score based on the 7-point severity scale. - All records were included in the Safety Population in the current analysis.

No

Exclusion Criteria

- Any cases identified that do not meet the inclusion criteria were excluded, including cases not treated with CroFab.

Locations

Location

Status