Clinical trials

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

Condition / disease
Location
Status: Recruiting

Efficacy and Safety of a Combined Dexmedetomidine-Ketamine Sedation Regimen for Pediatric Cardiac Catheterization

The goal of this observational study is to learn if the spontaneous sedation regimen of dexmedetomidine-ketamine (KETADEX) has the comparable efficacy and safety in pediatric cardiac catheterization versus the traditional regimen. The main question it aims to answer is: Is the combined Dexmedetomidine-Ketamine spontaneous sedation regimen (KETADEX) non-inferior to the traditional general anesthesia regimen in terms of efficacy and safety? Participants would received either KETADEX regimen or general anesthesia regimen. Research members then observe the catheterization procedure and answer the questionnaire about their efficacy and safety.

Participants needed: 150
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: National Children's Hospital, VietnamUpdated: May 4, 2026Locations: 1
Eligibility criteria

Patients under 18 years of age. [+1]

Patients with acute respiratory infections, chromosomal abnormalities, metabolic... [+2]

Status: Recruiting

Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy in Vietnam

This study aims to evaluate the effectiveness of therapeutic hypothermia in neonates diagnosed with hypoxic-ischemic encephalopathy (HIE). The study focuses on assessing both short-term outcomes after treatment and long-term neurological outcomes following therapeutic hypothermia.

Participants needed: 120
Trial details
Age: 0-6Biological sex: AllType: InterventionalSponsor: National Children's Hospital, VietnamUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Neonates diagnosed with hypoxic-ischemic encephalopathy (HIE) at the Neonatal Ce... [+6]

Presence of major congenital anomalies, particularly involving the central nervo... [+2]

Status: Recruiting

Autologous Bone Marrow Mononuclear Cell Transplantation Combined With Rehabilitation in Children With Sequelae of Hypoxic-Ischemic Encephalopathy or Intracranial Hemorrhage

This study evaluates the safety and preliminary efficacy of autologous bone marrow mononuclear cell transplantation combined with rehabilitation in children with neurological sequelae caused by hypoxic-ischemic brain injury or intracranial hemorrhage. Participants in the intervention group will receive autologous bone marrow aspiration, mononuclear cell transplantation via intrathecal route, and rehabilitation, while the control group will receive rehabilitation alone. Outcomes will be compared between groups over follow-up time points.

Participants needed: 60
Trial details
Age: 6-18Biological sex: AllType: InterventionalSponsor: National Children's Hospital, VietnamUpdated: Apr 14, 2026Locations: 1
Eligibility criteria

Children diagnosed with cerebral palsy [+5]

Children with acute infection at the time of screening or enrollment [+6]