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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04504656
Other study ID # Esophageal replacement
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2020
Est. completion date October 1, 2022

Study information

Verified date August 2020
Source Assiut University
Contact Ahmed Maher, Msc.
Phone 01026338229
Email ahmedmaherali31@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

a comparative prospective study of postoperative between minimally invasive and open surgery complications for esophageal replacement in children


Description:

Esophageal replacement in childhood is indicated in esophageal atresia patients with long-gap defects or following complications of primary esophageal anastomosis, as well as in patients with trauma and scarring to the esophagus following caustic ingestion. It is widely accepted that the ideal esophageal replacement is one that resembles the function of the native esophagus with minimal deterioration over time. Several techniques of esophageal replacement have been developed. These have focused mainly on the use of native tissues (including the stomach, jejunum, and colon) as conduits (1), attempts to use a synthetic prosthesis have been largely unsuccessful. In an attempt to reduce the trauma and morbidity associated with laparotomy and thoracotomy incisions, minimally invasive techniques are increasingly used. (2-4). Meta-analyses of adult esophagectomy for the treatment of esophageal cancer support the use of minimally invasive surgery (5) however, equivalent comparative studies in the pediatric population are lacking. As such, it is unclear whether minimally esophageal replacement is as safe as the open procedure in children. The present study aims to address this question by comparing the postoperative outcomes of children who underwent minimally invasive versus open esophageal replacement procedures at single-center and multicenter levels.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

All children undergoing oesophageal replacement aged one to 18 years. Due to

1. long gap esophageal atresia

2. caustic ingestion

3. congenital esophageal stenosis or strictures

Exclusion Criteria:

- patient who underwent previous esophageal replacement operations.

Study Design


Intervention

Other:
observation of postoperative leak, stenosis, mortality
detect complications in both groups

Locations

Country Name City State
Egypt Assiut University Children Hospitals Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anastamotic leaks Incidence of anastamotic leak which is identified clinically in both groups 2 years
Secondary Anastamotic stricture Incidence of symptomstic strictures which is identified by upper barium studies 2 years
Secondary Mortality Number of patient who die intraoperative and post operative in both groups 2 years
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