Ciprofloxacin effectiveness of the assessment to prevent bacterial infection of patients victims of accidents with snake in the Brazilian Amazo

Phase 4

Recruiting

• Conditions: C26.176.724; Secondary bacterial infection among snakebite victimsSnake venom; snake bite; T63.0

• Registration Number: RBR-3h33wy
• Lead Sponsor: niversidade do Estado do Amazonas

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-04-08
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

To have less than 24 hours of the accident; did not to use any antibiotics before answering the institution; to have not done the antivenom for the current snakebite ; to have no abscess or infection clearly established at the time of admission ; not to be allergic to the antibiotic of choice in this study ; not to be pregnant and not accept participate.

Exclusion Criteria

have mental inability to understand the objectives of the study and participate in the survey; have acute or chronic unstable; unavailability of stay in hospital for seven days to follow.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of secondary infection snakebite by 50% for patients in the group treated with antibiotic therapy early - intervention group. The primary endpoint for the occurrence of infection understand the time of recruitment until 48 hours after the intervention.

Secondary Outcome Measures

Name	Time	Method
Determining a clinical score for bacterial infection and possible early detection for protocol establishment of the event by markers of laboratory tests and clinical outcome.The secondary outcome for the occurrence of infection comprise the period after 48 hours to 7 days after the intervention.