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

Early empirical antibiotic therapy: a randomized clinical trial for superiority of a ciprofloxacin versus placebo in for preventing secondary bacterial infection among snakebite victims in the Brazilian Amazon

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-3h33wy
Enrollment
Unknown
Registered
2016-04-08
Start date
2014-07-10
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Secondary bacterial infection among snakebite victims Snake venom

Interventions

Use of early empirical antibiotic therapy for Treatment of the secondary infection in the snakebite.The two groups will initially be hospitalized and followed for at least seven (7) days. Experimental
Drug
N02.421.143.827.363
D03.438.810.835.322.186

Sponsors

Universidade do Estado do Amazonas
Lead Sponsor
Fundação de Amparo à Pesquisa do Estado do Amazonas
Collaborator

Eligibility

Age
1 Years to 100 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactJacqueline Sachett

Universidade do Estado do Amazonas

jac.sachett@gmail.com+55 (92) 81518086

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 26, 2026