Spontaneous Evisceration of Infantile Umbilical Hernia

• Sponsor: Ahmed Kamel Ali Mohamed (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05852535
• Collaborator: (none)
• Enrollment: 1
• Location: 1
• Anticipated Duration (Days): 17
• Patients Per Site Per Month: 1.8

Study Details

Study Description

Brief Summary

Infantile umbilical hernia is common in children. It has a regressive course in most cases. Conservative management is the standard in most cases before the age of 3 years unless there are complications such as incarceration, rupture with evisceration which are extremely rare and warrants emergency surgery.

We present a rare case of a 6-month-old child with sudden spontaneous evisceration of infantile umbilical hernia.

Condition or Disease	Intervention/Treatment	Phase
Pediatric Disorder	Procedure: Exploration

Detailed Description

Infantile umbilical hernia is common in children. It has a regressive course in most cases. Conservative management is the standard in most cases before the age of 3 years unless there are complications such as incarceration, rupture with evisceration which are extremely rare and warrants emergency surgery.

We present a rare case of a 6-month-old child with sudden spontaneous evisceration of infantile umbilical hernia.

Study Design

• Study Type: Observational
• Anticipated Enrollment: 1 participants
• Observational Model: Case-Only
• Time Perspective: Retrospective
• Official Title: Spontaneous Evisceration of Infantile Umbilical Hernia
• Anticipated Study Start Date: May 7, 2023
• Anticipated Primary Completion Date: May 23, 2023
• Anticipated Study Completion Date: May 24, 2023

Arms and Interventions

Arm	Intervention/Treatment
case report	Procedure: Exploration; abdominal exploration

Outcome Measures

Primary Outcome Measures

1. hospital stay [From April 1, 2023 to April 1, 2024]

   hospital stay

Eligibility Criteria

Criteria

• Ages Eligible for Study: 1 Month to 3 Years
• Sexes Eligible for Study: Male

Inclusion Criteria:

• Pediatric group

Exclusion Criteria:

• Adult group

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Ahmed Ali	Assiut		Egypt	71111

Sponsors and Collaborators

• Ahmed Kamel Ali Mohamed

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Ahmed Kamel Ali Mohamed, Mr., Assiut University
• ClinicalTrials.gov Identifier: NCT05852535
• Other Study ID Numbers: AKA171292
• First Posted: May 10, 2023
• Last Update Posted: May 10, 2023
• Last Verified: May 1, 2023

• Individual Participant Data (IPD) Sharing Statement: Yes
• Plan to Share IPD: Yes
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Hernia, Umbilical

Study Results

No Results Posted as of May 10, 2023