NCT06931912Active, not recruiting
Growth Evaluation, Health Promotion, and Clinical Management in Children and Adolescents With Thalassemia
Source: ClinicalTrials.gov · Last updated 18 Sept 2026
Brief summary (registry, in English)
There are nearly 300,000 patients with severe or intermediate thalassemia in China. Growth retardation is the most significant health issue for children and adolescents with transfusion-dependent thalassemia (TDT), placing a substantial economic burden on their families and a serious social strain on the labor force. Investigating the growth and development of these children and adolescents, and establishing targeted intervention plans, holds significant social value for public health practice. 1. To screen and identify pediatric patients with growth problems by conducting growth and development assessments in high-incidence areas of China, including physical development, endocrine function, nutritional status, brain function and lifestyle behaviors. 2. Implement the MENBS clinical interventions for pediatric patients with growth problems, concentrating on the following areas: * Monitor: Continuously monitor health-related indicators through regular follow-up. * Education: Provide health education to improve the cognition of patients and their families. * Nutrition: Assess patients' nutritional risks and develop personalized diet plans. * Behavior: Recommend appropriate exercise plans to promote physical development. * Support: Conduct home visits, offer free clinics and establish a support network. 3. Repeat growth assessment for pediatric patients with growth problems after 1-year clinical interventions. 4. Evaluate the effectiveness of MENBS interventions by comparing changes in growth and development indicators.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 385 (estimated)
- First submitted
- 7 Jan 2025
- Start date
- 1 Dec 2024
- Primary completion date
- 31 Oct 2026
- Lead sponsor
- Institute of Hematology & Blood Diseases Hospital, China
- Diseases
- Thalassaemia
- NCT number
- NCT06931912
What you commit to
- Study type: Interventional
- Planned participants: 385
- From 1 Dec 2024 to the primary completion date, 31 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Subjects received allo-HSCT or gene therapy
Other
- Subjects with clinically significant thyroid dysfunction
Who the study is looking for
- Subjects diagnosed with transfusion-dependent thalassemia (TDT)
- Male or female age ≤19 years
- Subjects who are willing and able to provide written informed consent
Age in the registry: - to 18 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Regenerative Medicine Center and Red Blood Cell Disorders Center Coordinator of this site? Confirm its status | Tianjin | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.