Pediatric Post-operative Abdominal Wound Dehiscence in Association With Midline vs Other Incisions: A Prospective Cohort Study
NCT ID: NCT05963477
Last Updated: 2023-07-27
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
270 participants
OBSERVATIONAL
2018-11-01
2020-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Continuous Versus Interrupted Suturing on Wound Dehiscence and Infection After Abdominal Surgery
NCT07241507
Comparison Between Conventional and Modified Smead Jones Method for Mass Closure in Emergency Midline Laparotomy
NCT05199974
The Suture Size in Laparotomy Wound Closure to Prevent Post-operative Complications
NCT05474677
Incisional Hernia in Infants and Children
NCT05005663
Surgical Management Of Gastroschisis
NCT06461325
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Age Group
Neonates Infants Children
laparatomy
all abdominal procedures which are approached by different incisions
Gender
Male Female
laparatomy
all abdominal procedures which are approached by different incisions
Selective/Emergency
Selective Emergency
laparatomy
all abdominal procedures which are approached by different incisions
Wound Class
Clean Clean-contaminated Contaminated Infected
laparatomy
all abdominal procedures which are approached by different incisions
Risk Factors
Yes No
laparatomy
all abdominal procedures which are approached by different incisions
Type of Incisions
Midline Trransverse Oblique
laparatomy
all abdominal procedures which are approached by different incisions
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
laparatomy
all abdominal procedures which are approached by different incisions
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
1 Day
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
French Medical Institute for Mothers and Children
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Abdullah Bahloli
Dr. Abdullah Bahloli
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
French Medical Institute for Mothers and Children
Kabul, , Afghanistan
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
40-FMIC-ER-18
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.