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NCT05510362 Clinical Trial

Management and Short Term Outcome of Traumatic Wounds in the Emergency Department

Wound Heal Clinical Trial

— SUTURES  

Official title:
Management and Short Term Outcome of Traumatic Wounds in the Emergency Department

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05510362
Other study ID # SUTURES
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 8, 2022
Est. completion date October 10, 2025

Study information
Verified date March 2024
Source University of Monastir
Contact Bel Haj ALI Khaoula, MD
Phone 29777277
Email belhajalikhaoula@yahoo.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Identify the risk factors for complications as well as study the evolution of wounds sutured in the emergency room towards complications such as superinfections, necrosis, disunity of the stitches linked to inadequate initial care.

Description:

All traumatic injuries should be considered contaminated upon presentation to the emergency room. This is why the main objective of this study was to describe the attitude of patients towards their wounds, to identify the risk factors for complications as well as to study the evolution of sutured wounds in the emergency room towards complications such as superinfections, necrosis, disunity of stitches linked to inadequate initial treatment. This is a prospective, observational, monocentric study carried out in the emergency services of the Fattouma Bourguiba hospital in Monastir.

Recruitment information / eligibility
Status Recruiting
Enrollment 3000
Est. completion date October 10, 2025
Est. primary completion date June 8, 2025
Accepts healthy volunteers No
Gender All
Age group 1 Year to 90 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Tunisia Nouira Monastir

Sponsors (1)
Lead Sponsor Collaborator
University of Monastir

Country where clinical trial is conducted

Tunisia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evolution of the wound and the healing period. After discharge from ED patients were called back in order to know information about the Suture complications(infection, release of stitches, hematoma, etc.) day 10
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