Clinical trials

10

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Letermovir Prophylaxis in Children With EBV-Positive T/NK-Cell Lymphoproliferative Disease and Refractory/Relapsed EBV-Associated Hemophagocytic Lymphohistiocytosis

This study investigates the impact of letermovir prophylaxis on viral infections (including CMV, EBV, BKV, HHV-6/7, RSV, ADV, HSV, etc.) following allogeneic hematopoietic stem cell transplantation in pediatric patients with EBV-associated T/NK-cell lymphoproliferative diseases and refractory/relapsed EBV-related hemophagocytic lymphohistiocytosis. Additionally, we examine its effects on other transplantation complications, including engraftment failure, graft-versus-host disease (GvHD), disease relapse, thrombotic microangiopathy (TMA), overall survival (OS), post-transplant lymphoproliferative disorder (PTLD) incidence, and immune reconstitution.

Participants needed: 80
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: Beijing Children's HospitalUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

Diagnosed with EBV-positive T/NK lymphoproliferative disease (EBV-T/NK LPD) acco... [+4]

History of CMV end-organ disease within 6 months prior to enrollment; [+8]

Status: Not yet recruiting

Research on Disease Control and Mental Health Status of Adolescent Asthma Patients

Background: Currently in China, adolescent asthma care is characterized by both undertreatment and overtreatment. Patients in this age group may exhibit negative emotions toward disease treatment and long-term control. Insufficient disease knowledge, irregular lifestyle habits, and negative attitudes toward the disease can all reduce medication adherence, affect disease control outcomes, and thereby increase the risk of severe chronic respiratory conditions and disease burden in adulthood. Objectives: To assess disease control status in adolescent asthma patients, evaluate the psychological well-being of patients and their family members, and understand patients' self-management skills and readiness for transition to adulthood. Procedures: Eligible participants will complete a series of assessment questionnaires through the Youran Huxi mobile application, including questionnaires on asthma control, physical activity, psychological health, self-management behaviors, and transition readiness. The study period is 12 months; the baseline assessment involves one-time completion of written questionnaires with no interim follow-up visits. The study does not intervene in clinical diagnosis or treatment decisions.

Participants needed: 460
Trial details
Age: 12-18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Feb 17, 2026
Eligibility criteria

Meet the asthma diagnostic criteria of GINA 2025 [+2]

Children with other respiratory diseases such as bronchiectasis, bronchiolitis,... [+1]

Status: Not yet recruiting

Control and Treatment of Outpatient Children With Asthma

The aim of this study is to comprehensively understand the disease control and management status of children with asthma in China, as well as the types of airway inflammation. The findings of this survey will help improve the asthma control level in Chinese children, facilitate future patient education, and guide rational medication use. Moreover, it will provide important evidence for health decision-making departments to better allocate and utilize medical resources.

Participants needed: 42,000
Trial details
Age: 2-18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Feb 17, 2026
Eligibility criteria

Age between 2 and 18 years old [+2]

With other respiratory diseases such as bronchiectasis, bronchiolitis, cystic fi... [+2]

Status: Recruiting

Hetrombopag in Promoting Platelet Engraftment After Auto-HSCT in Children With Neuroblastoma

The goal of this clinical trial is to learn if hetrombopag promotes platelet engraftment in neuroblastoma children undergoing autologous hematopoietic stem cell transplantation. The main question it aims to answer is: · Does drug hetrombopag promote platelet engraftment? Participants will take hetrombopag every day for 6 weeks or until platelet \> 100\*10\^9/L.

Participants needed: 30
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: Beijing Children's HospitalUpdated: Dec 3, 2025Locations: 1
Eligibility criteria

Age<18 years old; [+4]

ALT/AST > 3 ULN, or TBIL > 1.5 ULN; [+3]

Status: Not yet recruiting

Multicenter Pediatric Low-Dose CT Protocol: Development and Clinical Verification

Children are sensitive to ionizing radiation, and there are significant regional variations in current pediatric CT radiation doses. Although there are studies on low-dose CT targeting single lesions, these studies require clear clinical indications and support from advanced equipment, making widespread promotion difficult. The establishment of low-dose CT protocols is mostly experience-based; when radiologists lack confidence in image quality, the credibility of diagnostic reports is compromised. Therefore, the development of low-dose protocols must meet the diagnostic confidence of most radiologists, enable clear visualization of key anatomical structures in clinical practice, and satisfy the requirements for disease diagnosis. The purpose of this study is to establish a pediatric low-dose CT scanning protocol using Low-dose Simulation of CT (LDS) technology, and conduct a multicenter randomized controlled trial (RCT) in clinical settings to verify the clinical feasibility of this low-dose CT scanning protocol.

Participants needed: 2,650
Trial details
Age: 0-18Biological sex: AllType: InterventionalSponsor: Beijing Children's HospitalUpdated: Sep 30, 2025Locations: 20
Eligibility criteria

Aged 0-17 years. [+1]

Parents/guardians refuse to consent to low-dose CT examination. [+1]

Status: Recruiting

The Efficacy and Safety of PEGylated GH for the Treatment of Short Stature in Chinese Children-GLOBE Reg

In order to further observe the long-term safety and effectiveness of real-world polyethylene glycol-recombinant human growth hormone(PEG-rhGH) treatment of GHD, idiopathic short stature, and SGA in children, explore and analyze the factors affecting the efficacy of PEG-rhGH and the height prediction model after treatment, etc., collect and analyze more scientifically and rationally, and understand the situation of real-world PEG-GH treatment. A database registration study was developed.

Participants needed: 2,600
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Sep 4, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Improved Myeloablative Allogeneic Hematopoietic Stem Cell Transplantation Protocol for the Treatment of Epstein Barr Virus T/NK Lymphoproliferative Disease (EBV-T/NK LPD) and Prevention of Post Transplant Graft-versus-host Disease

To investigate whether the addition of recombinant humanized anti-CD25 monoclonal antibody to the conventional EBV-T/NK LPD conditioning regimen can prevent acute and chronic GVHD after transplantation, improve the severity of GVHD and have a corresponding impact on other related post-transplant complications such as poor engraftment, thrombotic microvascular disease, early EBV reactivation and relapse.

Participants needed: 48
Trial details
Phase: Phase 4Age: 0-18Biological sex: AllType: InterventionalSponsor: Beijing Children's HospitalUpdated: Jun 19, 2025Locations: 1
Eligibility criteria

Meet the diagnosis of EBV-T/NK lymphoproliferative disease (EBV-T/NK LPD) accord... [+4]

The expected survival period for multiple organ failure is no more than 3 months [+1]

Status: Recruiting

Population Pharmacokinetics of Anti-tuberculosis Drugs in Children With Tuberculosis

This study is based on the hypothesis that the pharmacokinetics of anti-tuberculosis drugs in TB children are different from adults. The investigators aim to study the population pharmacokinetics of children receiving the anti-tuberculsis drugs for treatment of TB. In this study, the investigators will detect drug concentration in plasma by using residual blood samples of blood gas analysis and other clinical tests and employ computers for constructing population pharmacokinetic models. In addition, the investigators also want to correlate use of anti-tuberculsis drugs with treatment effectiveness and incidence of adverse effects in children. This novel knowledge will allow better and more rational approaches to the treatment of TB in children. It will also set the foundation for further studies to improve anti-tuberculosis drug therapies for children.

Participants needed: 800
Trial details
Age: 1-18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Aug 15, 2018Locations: 1Duration: 18 Years
Eligibility criteria

Children (0-18 years old) with anti-tuberculosis therapy against TB. [+2]

Anti-tuberculosis drugs aren't involved in the therapies of children. [+3]

Status: Not yet recruiting

Registry Study on Cystic Fibrosis in Chinese Children

This study is a multicenter, prospective cohort study of patients diagnosed with cystic fibrosis, the clinical information of recruited patients, including clinical manifestations, lung function, chest imaging, quality of life and other indicators, will be followed for 10 years.

Participants needed: 100
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Apr 28, 2016
Eligibility criteria

Age 0~18 years old [+5]

It is unable to provide complete medical records or the current condition can no... [+1]

Status: Not yet recruiting

Registry Study on Primary Ciliary Dyskinesia in Chinese Children

This study is a multicenter, prospective cohort study of patients diagnosed with primary ciliary dyskinesia, the clinical information of recruited patients, including clinical manifestations, lung function, chest imaging, quality of life and other indicators, will be followed for 10 years.

Participants needed: 100
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Beijing Children's HospitalUpdated: Mar 10, 2016
Eligibility criteria

Age 0~18 years old [+8]

It is unable to provide complete medical records or the current condition can no... [+1]