- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06480344
Analysis of Risk Factors for Surgical Site Infections in Patients With Acute Abdomen at Hospital of State University of Haiti
June 27, 2024 updated by: Thaimye Joseph, University of Haiti
Risk Factors Associated With the Occurrence of Surgical Site Infections (SSI) in Patients Operated for Acute Abdomen at Hôpital de l'Université d'Etat d'Haiti (HUEH) From January 2018 to December 2020
The purpose of this study is to identify the risk factors associated with surgical site infection.
Study Overview
Status
Completed
Conditions
Detailed Description
87 patients medical records from January 2018 to December 2020 will be analyzed to detect the risk factors linked to the occurence of surgical site infection.
Then the strength of their association with surgical site infection will be determined via multivariate analysis.
Study Type
Observational
Enrollment (Actual)
87
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ouest
-
Port-au-Prince, Ouest, Haiti
- Hopital de l'Université d'Etat d'Haiti
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
The participants selected in our study include those who have developed an infection at the operating site (case) as well as those who have not developed it (controls) following acute abdominal surgery diagnosed in post-op room at the surgery department of The State University of Haiti, from January 2018 to December 2022.
Description
Inclusion Criteria:
- Female or male patients over 12 years of age.
- Admitted to the Surgery Department for acute surgical abdomen and having undergone surgery
Exclusion Criteria:
- Patients who have undergone abdominal surgery for urological or gynecological pathologies
- Files with missing information on preoperative, operative and post-operative arrangements
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Case
Patients who developed surgical site infection.
|
|
Controls
Patients who did not developed surgical site infection.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Occurence of surgical site infection
Time Frame: 1 year
|
Wheter or not patients developed surgical site infection
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2021
Primary Completion (Actual)
August 30, 2021
Study Completion (Actual)
August 30, 2021
Study Registration Dates
First Submitted
June 24, 2024
First Submitted That Met QC Criteria
June 27, 2024
First Posted (Actual)
June 28, 2024
Study Record Updates
Last Update Posted (Actual)
June 28, 2024
Last Update Submitted That Met QC Criteria
June 27, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- JTCVCC001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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