Clinical trials

6

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

Condition / disease
Location
Status: Not yet recruiting

A Longitudinal Study of Parental Sleep Intervention for Behavioral Insomnia in Early Childhood

The global incidence of mental illness among children and adolescents is rising, drawing increasing attention to early risk factors and preventive strategies. Behavioral sleep problems, which affect up to 50% of infants in the local population, are closely linked to impaired self-regulation-a core factor underlying many psychological disorders and a promising target for early intervention. Enhancing self-regulation may not only alleviate sleep problems but also mitigate long-term mental health risks. This study aims to develop an intervention toolkit based on current guidelines and high-quality evidence, integrating parent education with dynamic sleep assessment and longitudinal evaluation of self-regulation in infants. The project seeks to establish the efficacy of this approach, identify moderators of intervention outcomes, and provide an evidence base for personalized sleep interventions in clinical practice.

Participants needed: 30
Trial details
Age: 6-36Biological sex: AllType: InterventionalSponsor: Children's Hospital of Soochow UniversityUpdated: Feb 19, 2026
Eligibility criteria

Children aged 0-3 years. [+2]

Chronic diseases or history of head trauma. [+2]

Status: Recruiting

Observational Study on the Impact of Obstructive Sleep Apnea on Executive Function and Empathy Development in Children

This study aims to investigate the effects of obstructive sleep apnea (OSA) on executive function and empathy development in children aged 3-12 years. The study will compare the outcomes of different treatment approaches (surgical vs. pharmacological) in children with mild OSA and track the progression of cognitive and emotional functions over 12 months. The study will also explore potential EEG biomarkers for assessing neurological damage in OSA children.

Participants needed: 150
Trial details
Age: 3-12Biological sex: AllType: ObservationalSponsor: Children's Hospital of Soochow UniversityUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Children aged 3-12 years. [+3]

Other primary sleep disorders (e.g., narcolepsy, restless leg syndrome). [+2]

Status: Recruiting

Effectiveness of School-Based Time-Restricted Eating for the Prevention and Control of Obesity in Children

Childhood obesity has become a major global public health challenge. Obesity can not only affects children's physical and mental health during childhood but may also persist into adulthood, significantly increasing the risk of cardiovascular disease. Therefore, effective prevention and control of childhood obesity can shift the prevention window forward and promote the prevention of cardiovascular disease. Recently, time-restricted eating (TRE) has gained attention in adult studies for its feasibility, as it involves "time control without calorie restriction," demonstrating weight loss effects comparable to energy restriction and higher feasibility. Here, the investigators designed a school-based cluster randomized controlled trial to investigate the effectiveness of 12-hour TRE in preventing and controlling childhood obesity. Schools were randomly assigned to either the intervention group or the control group, and participants were recruited from each school at the class level, ensuring that each group included at least 690 children. The control group received routine health education, while the intervention group received 12-hour TRE in addition to routine health education. After a 9-month intervention period (one academic year), the two groups will be compared in terms of weight management and childhood obesity prevalence.

Participants needed: 1,380
Trial details
Age: 8-10Biological sex: AllType: InterventionalSponsor: Children's Hospital of Soochow UniversityUpdated: Sep 30, 2025Locations: 2
Eligibility criteria

The principal agrees to accept the randomization process and adhere to the study... [+8]

Individuals with a history of heart disease, high blood pressure, diabetes, tube... [+9]

Status: Recruiting

Peginterferon α-2b Injection for the Treatment of Pediatric RSV Bronchiolitis

This is a multicenter, randomized, positive-controlled, non-inferiority clinical study, planning to enroll 90 children with bronchiolitis caused by respiratory syncytial virus infection, to evaluate the safety and efficacy of inhaled Peginterferon α-2b injection compared to recombinant human interferon α2b in the treatment of pediatric respiratory syncytial virus bronchiolitis.

Participants needed: 90
Trial details
Age: 6-2Biological sex: AllType: InterventionalSponsor: Children's Hospital of Soochow UniversityUpdated: Feb 14, 2025Locations: 3
Eligibility criteria

The guardian of the child is able to understand the content, requirements, and l... [+6]

Extreme restlessness, drowsiness, coma, and possibly requiring mechanical ventil... [+7]

Status: Recruiting

Safety and Efficacy of Avapritinib in Relapsed or Refractory Pediatric CBF-AML With KIT Mutation

The purpose of this study is to evaluate the efficacy and safety of avapritinib in relapsed or refractory pediatric core binding factor acute myeloid leukemia with KIT mutation.

Participants needed: 50
Trial details
Phase: Phase 2Age: Up to 18Biological sex: AllType: InterventionalSponsor: Children's Hospital of Soochow UniversityUpdated: Aug 22, 2024Locations: 12
Eligibility criteria

Gender unlimited; [+11]

Have received prior treatment with avapritinib; [+6]

Status: Recruiting

Clinical Study of Induction Therapy Options Based on Molecular Subtyping and MRD in Children and Adolescents With AML

The goal of this clinical trial is to estimate the rate (probability) of complete remission or complete remission with incomplete count recovery (CR/CRi) with negative MRD after induction I and II, event-free survival (EFS), and cumulative incidence (probability) of relapse (CIR), in patients receiving molecular/precision medicine and MRD-driven remission inductions, and to assess secondarily if there is an improvement over the AML2018 protocol.

Participants needed: 500
Trial details
Phase: Phase 2Age: Up to 18Biological sex: AllType: InterventionalSponsor: Children's Hospital of Soochow UniversityUpdated: Aug 22, 2024Locations: 13
Eligibility criteria

1、Newly diagnosed, untreated AML; [+7]

1、Acute megakaryocytic leukemia (AMKL); [+11]