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Paediatric SurgeryASOS-PaedsNCT05061407

An African, Multi-centre Evaluation of Patient Care and Clinical Outcomes for Paediatric Patients Undergoing Surgery

An observational study of Paediatric Surgery and Perioperative/Postoperative Complications, run by University of KwaZulu at 2 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Access to safe surgery is a basic human right. This is highlighted by the work of the Lancet Commission on Global Surgery. There is a large burden of surgical disease in the paediatric surgical population with a large unmet need. Read more about this study

Who is it for?
Ages Up to 18 years
How many people
8,625 participants
Where
2 sitesin 2 countries
Study dates
15 Jan 2022to 1 Dec 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: All patients less than 18 years old, admitted to participating hospitals during the study period who undergo elective and non-elective surgery.

Who may be able to join

  • Consecutive patients < 18 years, admitted to participating hospitals during the study period
  • elective and non-elective surgery (including day case surgery)
  • operative procedures outside operating theatres where a general anaesthetic (GA) is performed.

Who cannot join

  • radiological or other procedures not requiring general anaesthesia, or where general anaesthesia is performed but no procedure is performed e.g. general anaesthesia during magnetic resonance imaging (MRI).
  • Obstetric surgery.
  • Prior participation in ASOS-Paeds.

Trial locations and contacts

2 sites in 2 countries.

2 sites in 2 countries

South Africa1 site
  • Inkosi Albert Luthuli Central Hospital

    Durban, KwaZuluNatal

Other trials in South Africa

Sudan1 site
  • Ribat Teaching Hospital

    Khartoum

Other trials in Sudan

About this study

Official title: An African, International Multi-centre Fourteen-day Evaluation of Patient Care and Clinical Outcomes for Paediatric Patients Undergoing Surgery (ASOS-Paeds)

Access to safe surgery is a basic human right. This is highlighted by the work of the Lancet Commission on Global Surgery. There is a large burden of surgical disease in the paediatric surgical population with a large unmet need. In Africa, children comprise a significant proportion of the population with approximately 50% of the population being ≤19 years old. Limited data from Africa suggests the risk factors for, incidence and outcomes associated with paediatric surgical complications differ from HICs.

The African Surgical Outcomes Study (ASOS) has described surgical outcomes in adult patients in Africa.

There is a need to determine the burden of the complications in paediatric surgical patients in Africa, and the risk factors for and the type of complications experienced. Once this study is completed, the investigators will be able to target appropriate interventions to improve surgical outcomes for children in Africa. The investigators have the capacity to do this important work, through the African Perioperative Research Group (APORG) group.

Read the detailed description

Surgery is a cost-effective public health intervention. There are significant disparities in access to and the safety of surgical and anaesthesia services in low and middle-income countries (LMICs) compared to high-income countries (HICs). There is a large burden of surgical disease in the paediatric surgical population with a large unmet need. In Africa, children comprise a significant proportion of the population with approximately 50% of the population being ≤19 years old.

Postoperative complications are an important determinant of surgical morbidity and mortality. Limited data from Africa suggests the risk factors for, incidence and outcomes associated with paediatric surgical complications differ from HICs. In the prospective, observational South African Paediatric Surgical Outcomes Study (SAPSOS), the patients in this middle-income country (MIC), had double the incidence of complications, and the types of complications differed from HICs, with a predominance of infective complications. Furthermore, the risk factors for complications (ASA physical status, urgency of surgery, severity of surgery and infective indication for surgery) were different from HICs, where risk factors include gestational age, ASA physical status >3, a history of cardiovascular disease, and cardiovascular, neurological, or orthopaedic surgical procedures. Postoperative mortality was ten times higher in South Africa than in a prospective study in HICs. A prospective study of paediatric perioperative mortality in 24 Kenyan hospitals showed a 7 day postoperative mortality of 1.7%, which is 17 times higher than that reported in HICs.

The African Surgical Outcomes Study (ASOS) has described surgical outcomes in adult patients in Africa. Patients had a lower risk profile and fewer complications compared to those in HICs. However, the postoperative mortality was twice that of the global average.

There is a need to determine the burden of the complications in paediatric surgical patients in Africa, and the risk factors for and the type of complications experienced. Once this study is completed, the investigators will be able to target appropriate interventions to improve surgical outcomes for children in Africa. The investigators have the capacity to do this important work, through the African Perioperative Research Group (APORG) group.

STUDY OBJECTIVE To determine the incidence of in-hospital postoperative complications up to 30 days post-surgery in paediatric surgical patients <18 years in Africa

STUDY DESIGN Fourteen-day, international African multi-centre prospective cohort study of paediatric patients (<18 years) undergoing surgery. This study will be registered on ClinicalTrials.gov. Patients will be followed up for a maximum of 30 days.

The primary outcome is the incidence of in-hospital postoperative complications in paediatric surgical patients in Africa. Secondary outcome measures include mortality rate for patients < 18 years undergoing surgery in Africa, risk factors associated with in-hospital complications, time from first presentation to operation, incidence of severe intraoperative critical incidents, level of qualification of anesthesia and surgery providers and number of specialists per paediatric population, and rate of admission to critical care.

The intention is to present a representative sample of paediatric surgical outcomes across all African countries. This study will run from October 2021 until December 2022.

ETHICS APPROVAL A waiver of consent has been approved by the IRB with the proviso that an approved broadcasting document and pictorial description are both placed for patients to see around the hospital and in the relevant wards. The requirement for patient consent is expected to vary according to regulations of the participating nations. the national leaders will ensure ethics approval is obtained form their respective countries and centres. Centres will not be permitted to record data unless ethics approval and an equivalent waiver is in place.

PREPARATORY WORK Prior leadership in the South African Paediatric Surgical Outcomes Study (SAPSOS) and the African Surgical Outcomes Study (ASOS) have ensured tested resource resources necessary to run this study. This will be the first continental collaborative study of paediatric surgical outcomes in Africa.

IMPORTANCE OF THIS STUDY Surgery is associated with significant morbidity. Accurate information regarding the burden of morbidity and mortality associated with paediatric surgery in Africa would allow for appropriate allocation of resources in the future, and the implementation of interventions to improve paediatric patient outcomes. This study therefore has important public health implications for Africa. This study will also provide the necessary data to develop future collaborative work to improve African surgical paediatric patient outcomes.

Medical subject headings
Postoperative Complications

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05061407
Study groupRoleWhat they receive
Paediatric surgical patientsAll patients < 18 years old, admitted to participating hospitals during the study period who undergo elective and non-elective surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postoperative complications

    Incidence of in-hospital postoperative complications in paediatric surgical patients in Africa.

    Measured: Until hospital discharge censored at 30 days postoperative

Secondary outcomes (6)
  1. Postoperative mortality

    1 a. The day of surgery mortality rate for patients < 18 years undergoing surgery in Africa.

    1. The in-hospital mortality rate for patients < 18 years undergoing surgery in Africa censored at 30 days.

    Measured: Until hospital discharge censored at 30 days postoperative

  2. Access to surgery

    Time from first presentation to operation

    Measured: Until hospital discharge censored at 30 days postoperative

  3. Intraoperative critical incidents

    Incidence of severe intraoperative critical incidents

    Measured: Until hospital discharge censored at 30 days postoperative

  4. Anesthesia and surgery providers

    Number of non-physician, nurse, physician (non-specialist), physician (specialist) anaesthesia and surgery providers

    Measured: Until hospital discharge censored at 30 days postoperative

  5. Rate of admission to critical care

    Percentage of patients requiring admission to critical care immediately postoperatively

    Measured: Until hospital discharge censored at 30 days postoperative

  6. Number of specialists per paediatric population

    Number of specialists per paediatric population

    Measured: Within 6 months of the start of recruitment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Sep 2021
  2. Study start15 Jan 2022
  3. Primary completion1 Dec 2022
  4. Study completion1 Dec 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
8,625 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05061407
Sponsor's protocol ID
ASOS-Paeds
Acronym
ASOS-Paeds
Status last verified
Mar 2025
First submitted
4 Sep 2021
Last updated
19 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • ASOS-Paeds Investigators. Outcomes after surgery for children in Africa (ASOS-Paeds): a 14-day prospective observational cohort study. Lancet. 2024 Apr 13;403(10435):1482-1492. doi: 10.1016/S0140-6736(24)00103-X. Epub 2024 Mar 22.

    PubMed 38527482

Questions about this trial

What is this clinical trial studying?

An observational study of Paediatric Surgery and Perioperative/Postoperative Complications, run by University of KwaZulu at 2 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in South Africa, Sudan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postoperative complications (time frame: Until hospital discharge censored at 30 days postoperative). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05061407, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Mar 2025.

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