A multicenter study of enhanced recovery after surgery in perioperative application of children with congenital choledochal cyst

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100044924

Enrollment

Unknown

Registered

2021-03-31

Start date

2021-04-15

Completion date

Unknown

Last updated

2021-11-02

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

Conditions

congenital choledochal cyst

Interventions

ERAS group:Adopting the concept of enhanced recovery after surgery for perioperative management

Traditional group:None

Eligibility

Sex/Gender

All

Age

No minimum to 14 Years

Inclusion criteria

Inclusion criteria: 1.Aged <=14 years, regardless of sex; 2.Preoperative imaging examinations (B-ultrasound, CT or MRI, etc.) indicate the diagnosis of choledochal cyst; 3.The patients legal representative signs the "Informed Consent".

Exclusion criteria

Exclusion criteria: 1.Associated with potentially life-threatening diseases of various organ systems; 2.Patients with pancreatitis and biliary perforation; 3.Caroli's disease; 4.Participated in other clinical trials in the last 3 months; 5.Any other circumstances that the investigator considers inappropriate to participate in the trial.

Design outcomes

Primary

Measure	Time frame
Postoperative hospitalization;	—

Countries

China

Contacts

Public ContactYang Heying

The First Affiliated Hospital of Zhengzhou University

yanghy130@163.com+86 13663713239

Outcome results

None listed

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