NCT03185637

Brief Summary

Background: Five billion people worldwide do not have access to safe, affordable surgical care. A significant proportion live in sub-Saharan Africa (SSA), where up to 50% of the population are children. There is limited literature on neonatal and paediatric surgery in SSA and children's surgery does not appear on any of the National Health Strategic Plans for the 47 independent countries across SSA. Objectives: To form a collaboration of surgeons and allied health professionals involved in children's surgery across SSA and collectively undertake the largest prospective cohort study of paediatric surgery in this region. Materials and Methods: Data will be collected via REDCap website on all patients with gastroschisis, anorectal malformation, appendicitis, inguinal hernia and intussusception, during a 1-month period of collaborators choice between October 2016 to April 2017, with a 30-day follow up until the end of May 2017. Estimated study population: 1450 patients from 50 institutions. Full ethical approval has been granted by the host centre; local ethical approval will be required at collaborating centres for participation. All collaborators will be co-authors. Primary outcome will be in-hospital all-cause mortality. Secondary outcomes will include post-intervention complications. Data will be collected on institutional facilities, patient demographics, duration from condition onset to presentation, peri-operative resuscitation, intervention and outcome. Differences in outcomes between SSA and benchmark data from high-income countries will be calculated using chi-squared analysis. Multi-level multivariate logistic regression analysis will be used to identify interventions and peri-operative factors associated with improved outcomes; p\<0.05 will be deemed significant. Outcome: Results will be used to advocate for enhanced children's surgical services in SSA. We shall identify context-appropriate interventions associated with improved outcome. The collaboration will help to enhance research capacity in the region.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,407

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2016

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2016

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2017

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

June 12, 2017

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 14, 2017

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2017

Completed
Last Updated

August 21, 2017

Status Verified

June 1, 2017

Enrollment Period

8 months

First QC Date

June 12, 2017

Last Update Submit

August 16, 2017

Conditions

Keywords

OutcomesMortalityComplicationsNeonatal surgeryPaediatric surgeryChildrens surgerySub-Saharan AfricaResearch CollaborationGastroschisisAnorectal malformationAppendicitisIntussuceptionInguinal hernia

Outcome Measures

Primary Outcomes (1)

  • All-cause in-hospital mortality

    In-hospital (if in the patient is still in hospital at 30-days post-intervention, a 30-day mortality will be utilised)

Secondary Outcomes (5)

  • 30-day mortality

    30-days

  • Duration of hospital stay

    Patients are followed up for a maximum of 30-days post-intervention

  • Surgical site infection

    Within 30-days post-intervention

  • Full thickness wound dehiscence

    Within 30-days post-intervention

  • Need for re-intervention

    Within 30-days of the primary intervention

Study Arms (5)

Gastroschisis

All patients presenting primarily to the institution with gastroschisis during the data collection period will be included in the study.

Procedure: Various interventions for each of the conditions.

Anorectal malformation

All patients presenting primarily to the institution with anorectal malformation during the data collection period will be included in the study.

Procedure: Various interventions for each of the conditions.

Appendicitis

All patients under 16-years of age presenting primarily to the institution with appendicitis during the data collection period will be included in the study.

Procedure: Various interventions for each of the conditions.

Intussusception

All patients under 16-years of age presenting primarily to the institution with intussusception during the data collection period will be included in the study.

Procedure: Various interventions for each of the conditions.

Inguinal hernia

All patients under 16-years of age undergoing surgery for an inguinal hernia at the institution during the data collection period will be included in the study.

Procedure: Various interventions for each of the conditions.

Interventions

This is an observational study. Patients were not allocated to different interventions. Common interventions for each of the conditions, which will be compared during analysis include the following: Gastroschisis - primary operative closure, surgical silo, preformed silo. Anorectal malformation - various types of stoma, anoplasty, PSARP, other. Appendicitis - antibiotics, open appendicectomy, laparoscopic appendicectomy. Intussusception - air enema reduction, hydro-enema reduction, laparotomy. Inguinal hernia - open repair, laparoscopic repair.

Anorectal malformationAppendicitisGastroschisisInguinal herniaIntussusception

Eligibility Criteria

AgeUp to 16 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)
Sampling MethodNon-Probability Sample
Study Population

Collaborating centres were recruited using convenience sampling with snowballing. Centres include both tertiary paediatric surgery centres and district hospitals.

You may qualify if:

  • All patients under 16-years of age presenting primarily with one of the five study conditions during the data collection period. This includes those managed conservatively without surgery or intervention and those offered palliative care, except patients with an inguinal hernia who must receive surgery to be included.

You may not qualify if:

  • Patients re-presenting with one of the five study conditions with a complication from a previous intervention or requiring further surgical intervention.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

King's Centre for Global Health and Health Partnerships

Denmark Hill, London, SE5 9RJ, United Kingdom

Location

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MeSH Terms

Conditions

GastroschisisAnorectal MalformationsAppendicitisIntussusceptionHernia, Inguinal

Condition Hierarchy (Ancestors)

Musculoskeletal AbnormalitiesMusculoskeletal DiseasesCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesHernia, AbdominalHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsDigestive System AbnormalitiesDigestive System DiseasesIntraabdominal InfectionsInfectionsGastroenteritisGastrointestinal DiseasesCecal DiseasesIntestinal DiseasesIntestinal Obstruction

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
30 Days
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 12, 2017

First Posted

June 14, 2017

Study Start

October 1, 2016

Primary Completion

May 31, 2017

Study Completion

June 30, 2017

Last Updated

August 21, 2017

Record last verified: 2017-06

Data Sharing

IPD Sharing
Will share

Following publication, the full anonymous data set will be made publicly available.

Locations