SC2i VIPER: EnVenomation Investigation Pilot to Evaluate Recovery

CompletedOBSERVATIONAL
Enrollment

15

Participants

Timeline

Start Date

May 5, 2017

Primary Completion Date

December 15, 2019

Study Completion Date

December 15, 2019

Conditions
Critical Illness
Interventions
OTHER

Research interventions of blood sampling and data collection

Patient-Specific Functional Scale (PSFS) survey will be administered to patients to record symptoms at both the time of evaluation in the emergency department and in follow up by phone at 3, 7, 14, 21 and 28 days after discharge from the emergency department or hospital. The rest of the patients' care will be as usual care, and patients will have had research interventions of blood sampling and data collection as noted in the previously approved SC2i Tissue Data Acquisition Protocol (TDAP) Pro00054947 (ClinicalTrial.gov ID: NCT02182180).

Trial Locations (1)

27710

Duke University Health Systems, Durham

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Uniformed Services University of the Health Sciences

FED

collaborator

United States Department of Defense

FED

collaborator

Duke University

OTHER

collaborator

Emory University

OTHER

collaborator

Grady Health System

OTHER

collaborator

Walter Reed National Military Medical Center

FED

lead

Henry M. Jackson Foundation for the Advancement of Military Medicine

OTHER

NCT03170297 - SC2i VIPER: EnVenomation Investigation Pilot to Evaluate Recovery | Biotech Hunter | Biotech Hunter