Understanding complications in traumatic wounds treated in the emergency room
Management and Short Term Outcome of Traumatic Wounds in the Emergency Department
This study looks at patients with traumatic wounds treated in the emergency room to see what factors might lead to complications like infections or tissue death.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3000 (estimated) |
| Ages | 1 Year to 90 Years |
| Sex | All |
| Sponsor | University of Monastir Academic / other |
| Locations | 1 site (Monastir) |
| Trial ID | NCT05510362 on ClinicalTrials.gov |
What this trial studies
This observational study aims to identify risk factors for complications in traumatic wounds treated in the emergency department. It focuses on the evolution of sutured wounds and the potential complications such as superinfections and necrosis that may arise from inadequate initial care. The study is conducted at the Fattouma Bourguiba hospital in Monastir, where patients presenting with acute suturable wounds will be monitored for outcomes. By analyzing these cases, the study seeks to improve understanding and management of wound care in emergency settings.
Who should consider this trial
Good fit: Ideal candidates for this study are patients presenting with acute suturable wounds at the emergency department.
Not a fit: Patients with wounds requiring surgical treatment, septic wounds, chronic lesions, or vascular wounds will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the management of traumatic wounds, leading to better patient outcomes and reduced complications.
How similar studies have performed: While this study focuses on a specific aspect of wound management, similar observational studies have shown success in identifying risk factors for complications in wound care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who presented to the ambulatory emergency circuit of the EPS Fattouma Bourguiba Monastir having as main reason for consultation an acute suturable wound. Exclusion Criteria: * Wounds requiring surgical treatment * Septic wounds * Chronic lesions * Vascular wounds * Patients who did not consent to the protocol.
Where this trial is running
Monastir
- Nouira — Monastir, Tunisia (Recruiting)
Study contacts
- Study coordinator: Bel Haj ALI Khaoula, MD
- Email: belhajalikhaoula@yahoo.fr
- Phone: 29777277
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.