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Oficialus tyrimo tekstas (anglų kalba)
Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation
- Atlanta Clinical Research Centers, Atlanta
- NSC Research, Inc, Johns Creek
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-28 · NCT07626411Safety in Adult Participants With Atrial Fibrillation Who Are Treated With Anticoagulation
- Grady Health System, Atlanta
- NSC Research, Inc, Johns Creek
Renkami dalyviai2 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-28 · NCT07175428Perivenous Dexamethasone Therapy: Examining Reduction of Inflammation After Thrombus Removal to Yield Benefit in Acute Femoropopliteal DVT
- Grady Memorial Hospital, Atlanta
- Piedmont Heart Institute, Atlanta
Renkami dalyviai2 fazė
Amžius nuo 18 iki 89 · Visoms lytims · Atnaujinta 2026-09-25 · NCT04862468Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation for Whom Oral Anticoagulation is Unsuitable
- Atlanta Clinical Research Centers, Atlanta
- NSC Research, Inc, Johns Creek
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-17 · NCT07430956ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders
- Comprehensive Bleeding Disorders Center at Emory University and Children's Healthcare of Atlanta, Atlanta
- Emory/Children's Health Care of Atlanta, Atlanta
- Memorial Health University Medical Center, Savannah
Renkami dalyviaiStebimasis tyrimas
Visi amžiai · Visoms lytims · Atnaujinta 2026-08-17 · NCT04398628Rapid Evacuation and Access of Cerebral Hemorrhage Trial
- Grady Memorial Hospital, Atlanta
- Emory Hospital Midtown, Atlanta
- Emory University Hospital (EUH), Atlanta
Renkami dalyviai
Amžius nuo 18 iki 70 · Visoms lytims · Atnaujinta 2026-08-14 · NCT06870812Neonatal Platelet Transfusion Threshold Trial
- Emory University, Atlanta
Renkami dalyviaiLaukiami sveiki savanoriai
1 Hour – 48 Hours · Visoms lytims · Atnaujinta 2026-03-25 · NCT06676904Iš ClinicalTrials.gov, duomenys gauti 2026-10-05. Kiekvienas tyrimas nustato savo tinkamumo kriterijus; tyrimo komanda sprendžia, kas gali dalyvauti.