Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The primary objective of the study is to evaluate the responsiveness and utility of several clinical outcome assessments in the setting of copperhead snakebite. The secondary objective is to characterize the clinical course of signs, symptoms and impairment during the recovery phase of copperhead snakebite.
This observational study will document the patient's recovery from copperhead snakebite. All care provided will be at the discretion of the treating physician in accordance with the local standard of care.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Patient Global Assessment of Recovery (PGAR) | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Numeric Pain Rating Scale (NPRS) | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Numeric Swelling Score (NSS) | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| SF36v2 (Acute Version) | Time of Discharge, Day 7, Day, 14, Day 21, and Day 28 | |
| Swelling Figure-of-8 Measurement | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Grip Strength | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Walking Speed | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Patient Global Impression of Change (PGIC) | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Return to Work/School/ADLs | Day 3, Day 7, Day 14, Day 21, and Day 28 | |
| Patient-Specific Functional Scale (PSFS) | Day 3, Day 7, Day 14, Day 21, and Day 28 |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Males and non-pregnant females at least 18 yrs of age with evidence of copperhead envenomation on an extremity distal to the knee or elbow that present for care at a health care facility within 24 hours of envenomation.
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Kentucky Chandler Medical Center | Lexington | Kentucky | 40536 | United States | ||
| LSU Health Sciences Center |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25975429 | Derived | Lavonas EJ, Gerardo CJ; Copperhead Snakebite Recovery Outcome Group. Prospective study of recovery from copperhead snake envenomation: an observational study. BMC Emerg Med. 2015 May 15;15:9. doi: 10.1186/s12873-015-0033-6. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| WPAI:SHP V2 | Day 3, Day 7, Day 14, Day 21, and Day 28 |
| Disorders of the Arm, Shoulder, and Hand (DASH) | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 |
| Lower Extremity Functional Scale | Time of Discharge, Day 3, Day 7, Day 14, Day 21, and Day 28 |
| Shreveport |
| Louisiana |
| 71103 |
| United States |
| University of Mississippi Medical Center | Jackson | Michigan | 39216 | United States |
| Washington University | St Louis | Missouri | 76104 | United States |
| Duke Medical Center | Durham | North Carolina | 27710 | United States |
| Vidant Health | Greenville | North Carolina | 27834 | United States |
| St. Joseph Regional Health Center | Bryan | Texas | 77802 | United States |
| Harris Methodist Hospital | Fort Worth | Texas | 76104 | United States |
| Scott and White Hospital | Temple | Texas | 76508 | United States |
| University of Virginia, Blue Ridge PC | Charlottesville | Virginia | 22908 | United States |
| Virginia Commonwealth University Richmond | Richmond | Virginia | 23219 | United States |