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Last updated 23 months ago
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Efficacy and Safety of Three Doses of Florence Oral Suspension in Adults With Eosinophilic Esophagitis
116 patients around the world
Available in
Brazil
EMS
1
Research sites
116
Patients around the world
This study is for people with
Esophagitis
Requirements for the patient
From 18 Years
All Gender
Medical requirements
Inclusion criteria
Signed consent;
Participants aged 18 years or more;
Participants diagnosed with eosinophilic esophagitis, defined as:
Presence of symptoms of esophageal dysfunction intermittently or continuously during previous week to the screening visit;
Eosinophilic esophageal inflammation with ≥ 15 eosinophils/high-power field, in the screening endoscopy;
Exclusion of other causes of esophageal eosinophilia.
Exclusion criteria
Any clinical and laboratory findings that, in the judgment of the investigator, may interfere with the safety of research participants;
Participants with a stricture on endoscopy that prevents passage of the endoscope;
History of alcohol abuse or drug use;
Use of concomitant therapies for any reason that may affect the assessment;
History of gastroesophageal surgery;
History of the abnormal gastrointestinal disorder;
Another disorder that causes esophageal eosinophilia;
Pregnancy or risk of pregnancy and lactating patients;
Participants with known allergy, contraindication or hypersensitivity to the components of the medicine used in the clinical trial;
Participation in clinical trial in the year prior to this study.
Sites
Allergisa
Recruiting
Consult
View site
Av. Dr. Romeu Tortima, 452 - Jardim Santa Genebra II (Barao Geraldo), Campinas - SP, 13084-791, Brazil
View site
Consult
See details
Contact us
Contact us
Sponsor
EMS
Study type
Interventional
Conditions
Requirements
From 18 Years
All Gender
Unique study ID
clinicaltrials.gov
NCT02873468
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