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Targeted thalidomide therapy in children with IBD

Building a risk-benefit model for thalidomide treatment in pediatric IBD patients using a genomics and metabolomics approach

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101132
Enrollment
Unknown
Registered
2025-04-21
Start date
2025-04-30
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Inflammatory bowel disease (IBD)

Interventions

Peripheral nerve injury group:NA
Tolerant Group:NA

Sponsors

Shenzhen Children’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Eligible patients were newly diagnosed or previously diagnosed pediatric patients with inflammatory bowel disease (IBD) confirmed at the Department of Gastroenterology, Shenzhen Children's Hospital, or those previously diagnosed according to the Lennard-Jones criteria and classified according to the Montreal classification; 2. Planning to take or currently taking thalidomide;

Exclusion criteria

Exclusion criteria: 1. Active Tuberculosis; 2. Malignant tumors; 3. children complicated by septicemia or requiring immediate surgery; 4. with significant abnormalities in the pulmonary, renal, hepatic, cardiac, hematologic, or neurological systems;

Design outcomes

Primary

MeasureTime frame
Thalidomide induced Peripheral Neuropathy;

Secondary

MeasureTime frame
SNP mutation status of candidate genes;Plasma endogenous small-molecule metabolite levels;Therapeutic effect of thalidomide;

Countries

China

Contacts

Public ContactJing Mao

Shenzhen Children’s Hospital

maoj5@mail2.sysu.edu.cn+86 755 83008256

Outcome results

None listed

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