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Migrena klinikiniai tyrimai Ilinoisas

6 tyrimai dėl Migrena ieško dalyvių vietose Ilinoisas.

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Oficialus tyrimo tekstas (anglų kalba)

Long-term Safety Study of Rimegepant in Pediatric Subjects for the Acute Treatment of Migraine

  • Chicago Headache Center & Research Institute, Chicago
  • AMR-Baber Research Inc, Naperville
Renkami dalyviai3 fazė
Amžius nuo 6 iki 17 · Visoms lytims · Atnaujinta 2026-09-24 · NCT04743141

Randomized Study in Children and Adolescents With Migraine: Acute Treatment

  • Chicago Headache Center & Research Institute, Chicago
  • AMR-Baber Research Inc, Naperville
Renkami dalyviai3 fazė
Amžius nuo 6 iki 17 · Visoms lytims · Atnaujinta 2026-09-24 · NCT04649242

Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets for the Acute Treatment of Migraine in Children and Adolescents (Ages 6-17)

  • Chicago Headache Center & Research Institute /ID# 248625, Chicago
  • Ascension Saint Alexius /ID# 275261, Hoffman Estates
Renkami dalyviai3 fazė
Amžius nuo 6 iki 17 · Visoms lytims · Atnaujinta 2026-09-14 · NCT05125302

A Study to Evaluate the Efficacy and Safety of Elismetrep (K-304) in the Acute Treatment of Migraine

  • Cedar Crosse Research Center, Chicago
  • Chicago Headache Center & Research Institute, Chicago
  • Healthcare Research Network II, LLC, Flossmoor
  • ir dar 1
Renkami dalyviai3 fazė
Amžius nuo 18 iki 75 · Visoms lytims · Atnaujinta 2026-08-20 · NCT07645924

Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks

  • Chicago Headache Center & Research Inst /ID# 272345, Naperville
Renkami dalyviaiStebimasis tyrimas
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-02-10 · NCT07310290

Effectiveness of Magnesium in Addition to Prochlorperazine for the Treatment of Migraines

  • Advocate Christ Medical Center Emergency Department, Oak Lawn
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-01-22 · NCT06904287

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