Paediatric

6

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

Condition / disease
Location
Status: Not yet recruiting

Relational Music Therapy Procedural Support for Paediatric Patients and Families Facing Repeated Invasive Procedures

This study explores how personalised music therapy can support children and their parents during repeated medical procedures, such as blood tests or injections. Many children find these procedures painful or frightening, and repeated experiences can lead to high anxiety and difficulty coping. Parents often feel distressed as well, which can affect how well they are able to support their child. Because children and parents regulate each other emotionally, helping both members of the pair is important for reducing distress. This study aims to explore how personalised music therapy-based procedural support (MTPS) influences the relational and emotional processes that help children and their parents cope, regulate, and build resilience during repeated medical procedures.

Participants needed: 20
Trial details
Age: 5-12Biological sex: AllType: InterventionalSponsor: Anglia Ruskin UniversityUpdated: Jul 2, 2026
Eligibility criteria

Paediatric patient (ages 5-12) undergoing recurring needle procedures (venipunct... [+4]

Patients currently under heavy sedation or anaesthetic medication that impairs c... [+4]

Status: Not yet recruiting

EFFECTS OF A THERAPEUTIC STRENGTH TRAINING PROGRAMME IN PAEDIATRIC CANCER PATIENTS

This project is made possible through the Pediatrics Department of the University Hospital of Salamanca, in collaboration with researchers specialized in therapeutic exercise from other clinical trials and research projects, alongside physical therapists experienced in designing, programming, and supervising therapeutic exercise programs. Furthermore, the project addresses current healthcare needs, as a significant portion of the patient population exhibits symptoms that impair functional capacity and overall quality of life-driven both by age and the oncological disease and its treatment. Consequently, this initiative aims to implement a strength training program to foster beneficial outcomes across various aspects of these patients' health, while sharing the findings with the scientific community.

Participants needed: 20
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: University of SalamancaUpdated: Jun 10, 2026
Eligibility criteria

People under the age of 18 who have been diagnosed with cancer and are currently... [+3]

Have any contraindications to physical exercise: severe musculoskeletal disorder... [+3]

Status: Recruiting

BELUGA: Better to Exchange ETT for LMA Before Extubation in Children Under General Anaesthesia

During surgery, anaesthetists can use an endotracheal tube (ETT) to facilitate ventilation. At emergence from general anaesthesia, there are two techniques for removal of the ETT: (1) the ETT is removed when the child is waking up in (awake removal); or (2) the ETT is removed while still under anaesthesia(deep removal). Currently there is no evidence to suggest either technique is safer - deep removal of the ETT may decrease the risk of overall airway complications, including cough and desaturations. However, it may be associated with increased airway obstruction compared with awake extubation in paediatric patients. In our institution, a further technique has become increasingly common practice: removing ETT deep to avoid coughing and desaturation, then inserting a laryngeal mask airway (LMA) which can be removed once the patient is awake in the postoperative care unit (PACU), avoiding the risk of airway obstruction coupled with deep airway removal. The aim of the study is to assess whether deep removal of an ETT and exchange to an LMA, is superior to awake ETT removal with regards to the occurrence of postoperative respiratory adverse events. In this study, patients will be randomised to awake removal of ETT or deep removal of an ETT and exchange to an LMA. Data will be collected regarding the rate of respiratory adverse events in either group, as well as the incidence of post-operative pain, delirium and nausea and vomiting.

Participants needed: 1,400
Trial details
Age: 0-16Biological sex: AllType: InterventionalSponsor: Telethon Kids InstituteUpdated: Jun 1, 2026Locations: 8
Eligibility criteria

5kg and above, [+2]

Children with severe cardiopulmonary disease or syndrome [+5]

Status: Not yet recruiting

Vegetarian Tube Feed Study

This is a single arm, prospective, single-centre study to evaluate the gastrointestinal tolerance and compliance over a 28-day period using a tube feed with food derived ingredients.

Participants needed: 25
Trial details
Age: 1-15Biological sex: AllType: InterventionalSponsor: Société des Produits Nestlé (SPN)Updated: Mar 12, 2026
Eligibility criteria

Patients from 1 -15 years requiring more than 50% of energy from tube feeding or... [+1]

No established tube feed. [+6]

Status: Recruiting

Infrared Thermography for Prediction of Successful Erector Spinae Plane Block in Unilateral Inguinal Hernia Surgery in Paediatric Patients

This study aims to evaluate the accuracy of temperature change (ΔT) measurements using infrared thermography to predict a successful erector spinae plane block in pediatric patients undergoing inguinal hernia repair under general anesthesia.

Participants needed: 69
Trial details
Age: 3-6Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Age from 3 months to 6 years. [+3]

Parents' or guardians' refusal [+7]

Status: Recruiting

Nutrition in Paediatric Critical Care

This is a multi-centre prospective cohort study of nutrition in paediatric critical care in Australia and New Zealand. The study is planned to run in parallel with the adult ICU cohort study, NUTRIENT. Two study periods are proposed with the first in late 2024 and the second in 2026. This observational study seeks to determine the following (although not limited to) descriptive outcomes of interest: 1. Nutritional outcomes, including route of nutrition support (oral, enteral and/or parenteral), energy and protein prescription and provision, and anthropometric measures 2. Patient-centred outcomes, including duration of invasive respiratory support and hospitalisation, and mortality 3. Nutrition service delivery in the PICU and ward settings

Participants needed: 200
Trial details
Age: 0-18Biological sex: AllType: ObservationalSponsor: Australian and New Zealand Intensive Care Research CentreUpdated: Nov 19, 2024Locations: 11
Eligibility criteria

All patients </=18 years of age [+2]

Those previously enrolled during the study period (i.e. those re-admitted to PIC... [+2]