Prevalence and Complications of Suture in the ED
Prevalence of Complications Post Sutured Wounds in the ED
1 other identifier
observational
250
1 country
1
Brief Summary
included patients who had sutured wounds in the ED were asked about complications after suture .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 2, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2021
CompletedFirst Submitted
Initial submission to the registry
March 2, 2022
CompletedFirst Posted
Study publicly available on registry
March 21, 2022
CompletedMay 16, 2023
May 1, 2023
2 years
March 2, 2022
May 13, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Sutures complications after discharge of the Emergency Department PART 1
After discharge from ED , patients were called back in order to know other informations about the patient and about the wound : its location,its dimension,the edges of the wound ,if its bleedong before suture ,and other factors that can facilitate its complications . the evolution of the wound, the adherence to the instructions and the prescriptions, the quality of healing and the search for complications
15 days after the suture
Secondary Outcomes (1)
Sutures complications after discharge of the Emergency Department PART 2
45 days after the suture
Eligibility Criteria
Included patients presented to the outpatient emergency circuit of the EPS Fattouma Bourguiba Monastir having as main reason for consultation an acute suturable wound. The patients excluded are those who consulted for wounds requiring surgical treatment, septic wounds and patients who did not consent to the protocol.
You may qualify if:
- Patients with acute suturable wound
You may not qualify if:
- Wounds requiring surgical treatment Septic wounds Chronic lesions Vascular wounds Patients who did not consent to the protocol.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Emergency department of university hospital Fattouma Bourguiba of Monastir Monastir, Monastir Tunisia Monastir, Tunisia, 5000
Monastir, Monastir ,Tunisia, 5000, Tunisia
Study Officials
- PRINCIPAL INVESTIGATOR
Semir Nouira, Professor
University of Monastir
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
March 2, 2022
First Posted
March 21, 2022
Study Start
January 2, 2020
Primary Completion
December 31, 2021
Study Completion
December 31, 2021
Last Updated
May 16, 2023
Record last verified: 2023-05