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Construction and Demonstration of a Diagnostic and Treatment Evaluation Model for Peutz-Jeghers Syndrome in Children – A Rare Disease

Construction and Demonstration of a Diagnostic and Treatment Evaluation Model for Peutz-Jeghers Syndrome (PJS) in Children – A Rare Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101659
Enrollment
Unknown
Registered
2025-04-28
Start date
2025-04-28
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Peutz-Jeghers Syndrome

Interventions

Observation group:NA

Sponsors

Xi’an Children’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Meeting diagnostic criteria for PJS. 2. Age under 18 years at enrollment. 3. Provision of written informed consent by participants/parents/guardians.

Exclusion criteria

Exclusion criteria: 1.Coexisting monogenic genetic disorders. 2.Inability or unwillingness to comply with long-term follow-up.

Design outcomes

Primary

MeasureTime frame
Malignant tumor;Intussusception;Bowel obstruction;Gastrointestinal hemorrhage;Surgery;—

Secondary

MeasureTime frame
Other poor prognosis;—

Countries

China

Contacts

Public ContactYing Fang

Xi'an Children's Hospital

970910576@qq.com+86 186 0290 7819

Outcome results

None listed

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