Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
250 participants
OBSERVATIONAL
2020-01-02
2021-12-31
Brief Summary
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Detailed Description
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The data relevant to this study are obtained prospectively from a detailed questionnaire in the annex and a telephone call and they are completed retrospectively with the data collected in the computerized medical record.
At the healing period, between 15 days and 45 days after the suture, the investigators called the patients back in order to know the evolution of the wound, the adherence to the instructions and the prescriptions, the quality of healing and the search for complications (infection , loose stitches, hematoma, etc.)
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
12 Years
90 Years
ALL
Yes
Sponsors
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University of Monastir
OTHER
Responsible Party
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Pr. Semir Nouira
Professor
Principal Investigators
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Semir Nouira, Professor
Role: PRINCIPAL_INVESTIGATOR
University of Monastir
Locations
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Emergency department of university hospital Fattouma Bourguiba of Monastir Monastir, Monastir Tunisia Monastir, Tunisia, 5000
Monastir, Monastir ,Tunisia, Tunisia
Countries
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Other Identifiers
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suture
Identifier Type: -
Identifier Source: org_study_id
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