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Kraujo krešuliai klinikiniai tyrimai Tennessee

7 tyrimai dėl Kraujo krešuliai ieško dalyvių vietose Tennessee.

Miestai Tennessee

Oficialus tyrimo tekstas (anglų kalba)

Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation

  • Tennessee Center for Clinical Trials, Tullahoma
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

  • East Coast Institute for Research, Jefferson City, Jefferson City
Renkami dalyviai2 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-28 · NCT07175428

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

  • Apex Research Foundation, LLC, Jackson
  • Tennova TCMC, Knoxville
  • Vanderbilt Heart and Vascular Tullahoma, Cardiology and Vascular Associates, Tullahoma
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

  • Tennessee Center for Clinical Trials, Tullahoma
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

  • St. Jude Children's Research Hospital, Memphis
  • Vanderbilt University Medical Center, Nashville
Renkami dalyviaiStebimasis tyrimas
Visi amžiai · Visoms lytims · Atnaujinta 2026-08-17 · NCT04398628

Rapid Evacuation and Access of Cerebral Hemorrhage Trial

  • Vanderbilt University Medical Center, Nashville
Renkami dalyviai
Amžius nuo 18 iki 70 · Visoms lytims · Atnaujinta 2026-08-14 · NCT06870812

Neonatal Platelet Transfusion Threshold Trial

  • Vanderbilt University, Nashville
Renkami dalyviaiLaukiami sveiki savanoriai
1 Hour – 48 Hours · Visoms lytims · Atnaujinta 2026-03-25 · NCT06676904

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