Skip to content

Management and Outcomes of Congenital Anomalies in Low-, Middle- and High- Income Countries: A Multicentre, International, Prospective Cohort Study

Management and Outcomes of Congenital Anomalies in Low-, Middle- and High- Income Countries: A Multicentre, International, Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023685
Enrollment
Unknown
Registered
2019-06-07
Start date
2018-10-01
Completion date
Unknown
Last updated
2019-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

congenital anomalies

Interventions

seven cohorts:Nil

Sponsors

The Children' Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 16 Years

Inclusion criteria

Inclusion criteria: Any neonate, infant or child under the age of 16 years, presenting for the first time, with one of the study conditions can be included in the study. This only includes children who have NOT previously received any surgery for their condition (surgery includes patients who have previously received a stoma). Children who have received basic resuscitative and supportive care for their condition at a different healthcare facility and then been transferred to the study centre can be included. If a patient presents with more than one of the study conditions (for example oesophageal atresia and ARM), the details of each condition can be included within the study. However, only those conditions presenting within the study period should be included. For example, if a patient has previously had a duodenal atresia repair and then presents with Hirschsprungs disease during the study period, only the latter should be included in terms of management and outcomes. Patients presenting primarily with one of the study conditions who receive palliative care or no care must be included within the study to reflect true outcomes.

Exclusion criteria

Exclusion criteria: Any neonate, infant or child with one of the study conditions who has previously received surgery for their condition. If they have recently received surgery for their condition, were discharged and then represented with a complication of the surgery during the study period they should NOT be included in the study.

Design outcomes

Primary

MeasureTime frame
mortality;

Countries

China

Contacts

Public ContactQiang Shu

The Children' Hospital of Zhejiang University School of Medicine

shuqiang@zju.edu.cn+86 13906500193

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026