Clinical trials

3

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

Condition / disease
Location
Status: Recruiting

HR-MRI-Directed Tirofiban Therapy for Late-Window Acute Ischemic Stroke (TIAN)

This study aims to address the existing clinical challenges by introducing high-resolution magnetic resonance vessel wall imaging (HR-MRI), an advanced imaging technology, to achieve precise etiological classification in patients with acute ischemic stroke (AIS) beyond the time window. HR-MRI allows clear visualization of intracranial arterial wall structures and direct identification of key pathological features of the culprit vessel, including atherosclerotic plaques, vascular wall remodeling, and intracranial hemorrhage, thereby enabling reliable differentiation between intracranial atherosclerotic large artery atherosclerosis (ICAS-LAA) stroke and other etiological subtypes such as cardiogenic embolism. Based on the latest clinical demands and advances in imaging technology, this study intends to evaluate the efficacy and safety of tirofiban in patients with ICAS-LAA stroke beyond the time window under the precise guidance of HR-MRI. It is expected to provide high-level evidence-based medical evidence for this specific patient population and further optimize clinical diagnosis and treatment strategies.

Participants needed: 458
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Weifang Medical UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years old; [+5]

Planned to receive reperfusion therapy (endovascular therapy or intravenous thro... [+16]

Status: Not yet recruiting

The Effects of Exercise Snacks on Endothelial Function and Body Composition in Overweight Individuals

This randomized controlled trial investigates the effects of two types of stair-climbing exercise snacks versus moderate-intensity continuous training on vascular health, body composition, and blood lipids in overweight or obese adults. Participants will be assigned to one of four groups for 6-8 weeks. The control group receives no exercise intervention. Primary outcomes include endothelial function (ultrasound), body composition (InBody), and lipid profile (blood test).

Participants needed: 60
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Weifang Medical UniversityUpdated: Apr 30, 2026
Eligibility criteria

Age: 18-35 years old (male, female); [+4]

There are other serious diseases, such as tumors; [+12]

Status: Not yet recruiting

The Effectiveness of a Virtual Reality-based Multisensory Intervention

This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery.

Participants needed: 100
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Weifang Medical UniversityUpdated: Apr 11, 2025
Eligibility criteria

Not listed