Prognostic Value of Transcranial Doppler Ultrasound in the Clinical Evolution of Patients With Acute Ischemic Stroke. The TRADE-AIS Study
Launched by JOSE IVAN RODRIGUEZ DE MOLINA SERRANO · May 27, 2025
Trial Information
Current as of August 19, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The TRADE-AIS study is a clinical trial that aims to understand how certain measurements taken from a test called transcranial Doppler ultrasound (TCD) can help predict how well patients will recover after having an acute ischemic stroke, which is when blood flow to the brain is blocked. The study will look specifically at the flow of blood in a major brain artery and how this relates to improvements in the patient's neurological condition over a short period. It will also examine other factors that might influence recovery, such as the presence of alternative blood flow routes in the brain.
To participate in this study, individuals must be at least 18 years old and have been diagnosed with an acute ischemic stroke within the last 24 hours. They will need to undergo the TCD test within this timeframe and be able to provide consent for participation. It's important to note that individuals with certain conditions, like bleeding in the brain or severe neurological diseases, won't be eligible. Those who join the study can expect to undergo a TCD test and have their recovery monitored to see how well they improve after the stroke. The trial is not yet recruiting participants, but it aims to provide valuable insights into stroke recovery.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥ 18 years
- • Clinical diagnosis of acute ischemic stroke
- • Onset of symptoms ≤ 24 hours before admission
- • Underwent or will undergo transcranial Doppler ultrasound within 24 hours of symptom onset
- • Able to provide informed consent or consent obtained from a legal representative
- Exclusion Criteria:
- • Evidence of intracerebral hemorrhage on imaging
- • Inadequate temporal acoustic window for transcranial Doppler
- • Intubated or hemodynamically unstable prior to Doppler evaluation
- • Known diagnosis of neurodegenerative disease significantly affecting baseline neurological function (e.g., advanced dementia, Parkinson's disease)
- • Refusal to participate or withdrawal of consent
About Jose Ivan Rodriguez De Molina Serrano
Jose Ivan Rodriguez de Molina Serrano is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and innovation. With extensive experience in overseeing clinical studies, he focuses on ensuring adherence to regulatory standards and ethical guidelines while fostering collaborative relationships with research institutions and healthcare professionals. His leadership is characterized by a strategic approach to trial design and execution, aimed at generating reliable data that contributes to the development of effective treatments and therapies. Passionate about improving patient outcomes, Rodriguez de Molina Serrano is dedicated to enhancing the integrity and efficiency of the clinical research process.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported