Pediatric Post-operative Abdominal Wound Dehiscence in Association With Midline vs Other Incisions: A Prospective Cohort Study

This study is designed to see different abdominal incisions complication among neonates, infants and children and to find risk factors for developing wound dehiscence

Completed

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Key information

Conditions

Wound Dehiscence Incision Surgical Wound Wounds and Injuries

Age range

1 day–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

French Medical Institute for Mothers and Children

Kabul, 1006, Afghanistan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

-all abdominal surgeries patient under 18-year-old.

Exclusion criteria

Umbilical hernia, redo laparatomy, laparoscopic surgery.

Treatment and study plan

laparatomy

Procedure

all abdominal procedures which are approached by different incisions

Primary outcomes

Wound dehiscence or burst abdomen

Time frame: one month after intervention

the overall outcome of the intervention (incisions) is wound dehiscence in different age groups, in gender, among who has or has no risk factors and among different wound class

Sponsors and collaborators

Lead sponsor

French Medical Institute for Mothers and Children

Other Gov

Registry information

Official study title

Pediatric Post-operative Abdominal Wound Dehiscence in Association With Midline vs Other Incisions in Tertiary Care Setting Kabul Afghanistan: A Cohort Study

Important dates

Study start: 2018
Primary completion: 2020
Study completion: 2020
First posted: Jul 27, 2023
Registry last updated: Jul 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed