NCT05289232

Brief Summary

included patients who had sutured wounds in the ED were asked about complications after suture .

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2020

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 2, 2020

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2021

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 2, 2022

Completed
19 days until next milestone

First Posted

Study publicly available on registry

March 21, 2022

Completed
Last Updated

May 16, 2023

Status Verified

May 1, 2023

Enrollment Period

2 years

First QC Date

March 2, 2022

Last Update Submit

May 13, 2023

Conditions

Keywords

suturecomplications

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

Age12 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

Study Officials

  • Semir Nouira, Professor

    University of Monastir

    PRINCIPAL INVESTIGATOR

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

Locations