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Kraujo krešuliai klinikiniai tyrimai Luiziana

7 tyrimai dėl Kraujo krešuliai ieško dalyvių vietose Luiziana.

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Oficialus tyrimo tekstas (anglų kalba)

Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation

  • Monroe Research, LLC, West Monroe
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-28 · NCT07626411

Safety in Adult Participants With Atrial Fibrillation Who Are Treated With Anticoagulation

  • Monroe Research, LLC, West Monroe
Renkami dalyviai2 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-28 · NCT07175428

Perivenous Dexamethasone Therapy: Examining Reduction of Inflammation After Thrombus Removal to Yield Benefit in Acute Femoropopliteal DVT

  • CIS Clinical Research, Houma
Renkami dalyviai2 fazė
Amžius nuo 18 iki 89 · Visoms lytims · Atnaujinta 2026-09-25 · NCT04862468

Reducing Adverse Vascular Outcomes With Factor XI Inhibition in Adult Participants With Peripheral Artery Disease

  • Cardiovascular Solutions, Shreveport
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-25 · NCT07318610

Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation for Whom Oral Anticoagulation is Unsuitable

  • Monroe Research, LLC, West Monroe
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-17 · NCT07430956

ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders

  • Louisiana Center for Bleeding and Clotting Disorders, Tulane University, New Orleans
Renkami dalyviaiStebimasis tyrimas
Visi amžiai · Visoms lytims · Atnaujinta 2026-08-17 · NCT04398628

The CoAGulation Biomarkers and Atrial Fibrillation (COAG-AF) Pilot Study

  • East Jefferson General Hospital, New Orleans
  • University Medical Center, New Orleans
  • Tulane Doctors - Speciality Care - Napoleon, New Orleans
Renkami dalyviaiStebimasis tyrimas
Amžius nuo 18 iki 120 · Visoms lytims · Atnaujinta 2026-03-05 · NCT04947657

Iš ClinicalTrials.gov, duomenys gauti 2026-10-05. Kiekvienas tyrimas nustato savo tinkamumo kriterijus; tyrimo komanda sprendžia, kas gali dalyvauti.