- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01631591
Prevalence of Food Allergies in a Cohort of Adult Patients With Eosinophilic Esophagitis (EE)
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Study Population Male and female subjects, ages 18 years and older with findings of > 15 eosinophils per high powered field by endoscopic esophageal biopsy. Patients should also have symptoms consistent with eosinophilic esophagitis including dysphagia, heartburn, epigastric pain, recurrent vomiting, or food impaction. The comparative group will include male and female subjects, ages 18 years and older with a previous diagnosis of gastroesophageal reflux with findings of < 15 eosinophils per high power field by endoscopic esophageal biopsy.
Inclusion Criteria
- Male and female subjects 18 years and older
- Previous diagnosis of eosinophilic esophagitis with clinical symptoms including heartburn, dysphagia, vomiting, epigastric pain, recurrent vomiting, food impaction as well > 15 eosinophils per high powered field (400x magnification) by endoscopic esophageal biopsy in both the proximal and distal esophagus
- Previous diagnosis of gastroesophageal reflux with < 15 eosinophils per high powered field (400x magnification) by endoscopic biopsy
Exclusion Criteria
- Male and female subjects less than 18 years of age
- Pregnant female subjects
- Subjects who are receiving systemic steroids and are unable to stop prior to enrollment
- Subjects who are receiving systemic antihistamines and are unable to stop prior to enrollment
- Subjects who are unable to cooperate/comply with study procedures or communicate with investigator in order to successfully complete the study
- Subjects with severe skin disorders such as atopic dermatitis, dermatographism, or psoriasis who would be unable to complete skin or patch testing
- Subjects with an infirmity, disability, or geographical location which seems likely to prevent regular attendance for patient visit Risks Skin testing with prick methodology has a risk of systemic reaction of less than 0.1% per 40 tests, however, no deaths have been reported with this method of testing. Systemic reactions are readily treated using Injectable epinephrine with oral antihistamines and oral corticosteroids (prednisone). Patch testing has no known associated risk for development of systemic reactions. Phlebotomy is associated with a minimal risk of bleeding, significant local discomfort, and infection from the needle puncture.
Benefits Treatment options for adults with eosinophilic esophagitis are limited. Food allergies are a known contributor to this disorder in children and a better understanding of food allergies in adult subjects may provide additional treatment options.
Adverse Events and Withdrawal Criteria All subjects will be assessed for adverse events at each study visit. If any adverse events are experienced by the subject, the investigator will document the event within the subject's file and promptly report the event to the IRB. The investigators involved with this study will determine if a participant needs to be withdrawn from the study based upon the subject's health and medical history.
Sample Size Sample size estimation is based on the assumption that up to 50% of adults with eosinophilic esophagitis (EE) will have a positive skin test to food and 10% of adults without EE will have a positive skin test to food. With this assumption, a total of 40 subjects are needed, 20 per group, in order to achieve at least 80% power with two sided test at alpha level of 0.05 and beta 0.2.
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
Florida
-
Tampa, Florida, Forenede Stater, 33613
- University of South Florida
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Male and female subjects 18 years and older
- Previous diagnosis of eosinophilic esophagitis with clinical symptoms including heartburn, dysphagia, vomiting, epigastric pain, recurrent vomiting, food impaction as well > 15 eosinophils per high powered field (400x magnification) by endoscopic esophageal biopsy in both the proximal and distal esophagus
- Previous diagnosis of gastroesophageal reflux with < 15 eosinophils per high powered field (400x magnification) by endoscopic biopsy
Exclusion Criteria:
1. Male and female subjects less than 18 years of age 2. Pregnant female subjects 3. Subjects who are receiving systemic steroids and are unable to stop prior to enrollment 4. Subjects who are receiving systemic antihistamines and are unable to stop prior to enrollment 5. Subjects who are unable to cooperate/comply with study procedures or communicate with investigator in order to successfully complete the study 6. Subjects with severe skin disorders such as atopic dermatitis, dermatographism, or psoriasis who would be unable to complete skin or patch testing 7. Subjects with an infirmity, disability, or geographical location which seems likely to prevent regular attendance for patient visit
-
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: Andet
- Tidsperspektiver: Andet
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
eosinophilic esophagitis
PATIENTS WITH A CURRENT DIAGNOSIS OF eosinophilic esophagitis.
|
|
GERD
PATIENTS WITH A DIAGNOSIS WITH GERD.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Prevalence of food allergies in a cohort of adult patients with EE.
Tidsramme: Study to close on or around May 2014
|
Study to close on or around May 2014
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- eosinophilic esophagitis
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Eosinofil øsofagitis
-
Humanis Saglık Anonim SirketiAfsluttetHELICOBACTER PYLORI INFEKTIONER | Erosiv gastritis | Erosiv esophagitis (EE)Jordan
-
Indonesia UniversityIkke rekrutterer endnuErosiv esophagitisIndonesien
-
Braintree LaboratoriesAfsluttetErosiv esophagitisForenede Stater
-
Phathom Pharmaceuticals, Inc.AfsluttetErosiv esophagitisForenede Stater, Polen, Bulgarien, Det Forenede Kongerige, Tjekkiet, Ungarn
-
Daewoong Pharmaceutical Co. LTD.Hanyang UniversityUkendtErosiv esophagitisKorea, Republikken
-
TakedaAfsluttetEffekt og sikkerhed af oral Vonoprazan én gang dagligt (TAK-438) hos deltagere med erosiv øsofagitisErosiv esophagitisKina, Taiwan, Korea, Republikken, Malaysia
-
AstraZenecaAfsluttetGastroøsofageal reflukssygdom (GERD) | Erosiv esophagitis | Ikke-erosiv esophagitisForenede Stater, Frankrig, Italien, Belgien
-
Shandong Luoxin Pharmaceutical Group Stock Co.,...AfsluttetErosiv esophagitis (EE)Kina
-
Konkuk University Medical CenterDaewoong Pharmaceutical Co. LTD.RekrutteringErosiv esophagitisKorea, Republikken
-
Boryung Pharmaceutical Co., LtdAfsluttet