Clinical Trials Logo

Clinical Trial Summary

This study is a multi-centre interventional study at seven tertiary paediatric surgery centres in Ghana, Zambia, Malawi and Tanzania aimed at reducing mortality from gastroschisis.


Clinical Trial Description

Background: Gastroschisis has a great disparity in outcomes globally with less than 4% mortality in high-income countries (HICs) and over 90% mortality in many tertiary paediatric surgery centres across sub-Saharan Africa (SSA), including the study centres. Low-technology, cost-effective, evidence-based interventions are available with the potential for improved outcomes in low-resource settings.

Aim: To develop, implement and prospectively evaluate an interventional care bundle to reduce mortality from gastroschisis in seven tertiary paediatric surgery centres across SSA.

Study Design: A hybrid type 2 effectiveness-implementation study design will be utilised, which focusses equally on the effectiveness of the intervention through analysing clinical outcomes and effectiveness of the implementation through analysis of service delivery and implementation outcomes.

Methods: Using current literature an evidence-based, low-technology interventional care bundle has been developed with both pre-hospital and in-hospital components. During 2018 a systematic review, qualitative study and Delphi process will provide further evidence in order to optimise the interventional bundle and implementation strategy for use in low-resource environments. The interventional care bundle has core components, which will remain consistent across the seven sites, and adaptable components, which will be determined through in-country co-development meetings with all relevant members of the multi-disciplinary team. Across the seven study sites it is estimated that 180-289 patients will be included in the study, which has the potential to determine a difference in pre- and post-intervention mortality between 10-15%.

Implementation will take place over a 4-week period at each of the study sites between April - December 2019. Pre- and post-interventional data will be collected on clinical, service delivery and implementation outcomes between September 2018 to October 2020 (2-years of patient recruitment at each site with a 30-day post primary intervention follow-up period). The primary clinical outcome will be all-cause, in-hospital mortality. Secondary outcomes include the occurrence of a major complication, length of hospital stay and time to full enteral feeds. Service delivery outcomes include time to hospital and primary intervention and adherence to the pre-hospital and in-hospital management protocols. Implementation outcomes will include acceptability, adoption, appropriateness, feasibility, fidelity, coverage, cost and sustainability.

Expected Results: Pre- and post-intervention clinical outcomes will be compared using Chi-squared analysis, unpaired t-test and/ or Mann-Whitney test. Time-series analysis will be undertaken using Statistical Process Control to identify significant trends and shifts in outcome overtime. Multivariate logistic regression analysis will be used to identify both clinical and implementation factors affecting outcome with adjustment for confounders. P<0.05 will be deemed significant.

Outcome: This will be the first multi-centre interventional study to the investigator's knowledge aimed at reducing mortality from gastroschisis in low-resource settings. If successful, detailed evaluation of both the clinical and implementation components of the study will allow sustainability in the study sites and further scale-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03724214
Study type Interventional
Source King's College London
Contact Naomi J Wright, MBChB BSc MRCS DCH MSc
Phone 0044 7824468954
Email paedsurg.research@gmail.com
Status Recruiting
Phase N/A
Start date October 8, 2018
Completion date January 31, 2021

See also
  Status Clinical Trial Phase
Completed NCT00539292 - Evaluating the Use of a Silastic Spring-Loaded Silo for Infants With Gastroschisis Phase 2
Recruiting NCT01469208 - Music Therapy: An Adjunct To Gastroschisis Infants' Care N/A
Terminated NCT00404690 - Bedside Silo Versus Operative Closure for Gastroschisis N/A
Recruiting NCT05704257 - Fetal Repair of Complex Gastroschisis: A Safety and Feasibility Trial N/A
Completed NCT03533439 - Regional Blood Saturation Levels in Gastroschisis
Active, not recruiting NCT03393832 - Oral Care in Infants With Gastroschisis
Completed NCT03666767 - Management and Outcomes of Congenital Anomalies in Low-, Middle- and High-Income Countries
Terminated NCT03355326 - Evaluation of Glycerin Suppositories to Improve Bowel Function in Gastroschisis Phase 4
Completed NCT03185637 - Children's Surgery in Sub-Saharan Africa N/A
Completed NCT02575846 - Clinical and Biological Outcomes of Human Milk and Formula Intake After Gastroschisis Repair N/A
Terminated NCT01094587 - Sutureless vs Sutured Gastroschisis Closure N/A
Active, not recruiting NCT00127946 - Trial of AMNIOECHANGE in Gastroschisis Affected Foetuses Phase 3
Withdrawn NCT04186039 - Functional Evaluation of the Fetal Lung by Functional Magnetic Resonance Imaging - Blood Oxygenation Level Dependent (MRI-BOLD), in Congenital Diaphragmatic and Parietal Malformations N/A
Active, not recruiting NCT06461325 - Surgical Management Of Gastroschisis
Completed NCT03960320 - Health Related Quality of Life of Patients With Abdominal Wall Defects
Terminated NCT02098915 - Metoclopramide Pilot Trial Phase 3
Completed NCT01316510 - Probiotics in Infants With Gastroschisis N/A
Completed NCT04020939 - The Role of Indocyanine Green Angiography Fluorescence on Intestinal Resections in Pediatric Surgery. N/A
Recruiting NCT06072976 - The Influence of Feeding Source on the Gut Microbiome and Time to Full Feeds in Neonates With Congenital Gastrointestinal Pathologies N/A
Recruiting NCT05293353 - Neokare Safety and Tolerability Assessment in Neonates With GI Problems