Pediatric Patients

4

Review clinical trials related to Pediatric Patients. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Neurocognitive Deficit After Paediatric Transplantation: Understanding the Role of Environment and Physical Function

Hematopoietic stem cell transplantation (HSCT) is a potentially life-saving treatment for children with relapsed or resistant leukemia and other life-threatening hematological and hereditary disorders. In Denmark, around 25 children undergo allogeneic HSCT every year, of these approximately 85-90% survive into adulthood. The goal of this observational study is to learn about neurocognitive outcomes in children undergoing (HSCT) and to understand which clinical, physical, and environmental factors may affect neurocognitive development during the first year after transplant. The main questions it aims to answer are: How does neurocognitive function change from before HSCT to one year after transplantation in pediatric patients? Which clinical, physical, and environmental factors are linked to better or worse neurocognitive outcomes? Participants will: Complete neurocognitive tests before HSCT and at 1-year follow-up, covering intelligence, memory, attention, executive function, processing speed, and motor skills. Undergo physical tests before HSCT, at hospital discharge, at 6-months follow-up, and at 1-year follow-up, including muscle strength, mobility, endurance, balance, and cardiopulmonary fitness (only at 1-year follow-up). Wear activity trackers to measure physical activity and sedentary time during hospitalization at 6 months and 1-year post-HSCT. Complete questionnaires about sleep, pain, quality of life, fatigue, family background, and exposure to outdoor and green spaces. Have medical records reviewed for treatment-related side effects, immune recovery, inflammation, and pain management. This study will help understand how neurocognitive function develops after HSCT in children and which factors (clinical, physical, or environmental) may support better recovery and well-being.

Participants needed: 100
Trial details
Age: 0-18Biological sex: AllType: ObservationalSponsor: Rigshospitalet, DenmarkUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Recipient of allogeneic HSCT in the study period [+3]

Status: Recruiting

Preoperative Gamified Breathing Exercise on Anxiety and Delirium in Children.

This study aims to evaluate the effect of preoperative gamified breathing exercises on preoperative anxiety and postoperative emergence delirium in children. The intervention includes games like ball blowing and bubble blowing. Anxiety is measured using the mYPAS-SF scale, and delirium is assessed with the PAED scale.

Participants needed: 80
Trial details
Age: 3-7Biological sex: AllType: InterventionalSponsor: Bozok UniversityUpdated: Feb 12, 2026Locations: 1
Eligibility criteria

Children aged 3 to 7 years (preschool age).

Status: Not yet recruiting

Impact of Conversational Approaches in Pediatric Social Robot-Mediated Interventions

This study examines how different robot dialogue systems (rule-based vs. large language model-based) and content types (emotional support vs. safety education) affect pediatric patients' responses during hospital-based robot-mediated interventions. Approximately 60 pediatric patients aged 2-9 years will be randomly assigned to interact with a social robot (LIKU) using either rule-based or LLM-based dialogue. Each child will participate in two activity sessions (emotional content and safety content) in randomized order. Primary outcomes include child engagement, emotional responses, robot perception, and activity preferences, assessed through standardized questionnaires (UEQ, Godspeed), child interviews, and behavioral observations. Additionally, 5 experts will evaluate content appropriateness and safety. This pilot study aims to provide foundational data for developing personalized pediatric robot programs in hospital settings, optimizing both dialogue approaches and content design based on individual child characteristics.

Participants needed: 60
Trial details
Age: 2-9Biological sex: AllType: InterventionalSponsor: Samsung Medical CenterUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Pediatric patients aged 2-9 years [+6]

Diagnosis of moderate to severe developmental delay (language or cognitive) docu... [+3]

Status: Recruiting

Ultrasound Guided Bilateral Pectoral Nerve Block Versus Bilateral Transverse Thoracic Plane Block In Pediatric Patients Undergoing Corrective Cardiac Surgeries Requiring Cardiopulmonary Bypass Via Median Sternotomy

This randomized, double-blinded, study aims to compare the efficacy of intraoperative and postoperative pain control while using bilateral ultrasound guided the pectoral nerves (PECS) versus transversus thoracic muscle plane block (TTPB) in pediatric patients undergoing corrective cardiac surgeries.

Participants needed: 81
Trial details
Age: 6-7Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: May 30, 2025Locations: 1
Eligibility criteria

Age: 6 months - 7 years. [+3]

Patients whose parents or legal guardians refuse to participate. [+11]