Oral Immunotherapy for Peanut and Mammalian Meat Allergies
NCT02350660 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2020-11-03
Summary
Pilot study to assess the effect of oral immunotherapy on specific Immunoglobulin E (IgE) levels and antigen consumption in two distinct food allergies.
Conditions
- Food Hypersensitivity
Interventions
- DIETARY_SUPPLEMENT
-
cow's milk
daily consumption of cow's milk
- DIETARY_SUPPLEMENT
-
peanut powder
peanut oral immunotherapy
Sponsors & Collaborators
-
University of Virginia
lead OTHER
Principal Investigators
-
Scott Commins, MD · University of Virginia
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 4 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-03-31
- Primary Completion
- 2014-09-30
- Completion
- 2015-06-30
Countries
- United States
Study Locations
More Related Trials
-
The Effect of Methylprednisolone on the Reversal Time of Rocuronium by Sugammadex in the Pediatric Patient Group
NCT06623370 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Dexamethasone on Sugammadex Reversal
NCT02137395 ·Status: COMPLETED ·Phase: PHASE4
-
Study With Medical Nutrition Product PTM202 in Pediatric Diarrhea
NCT01814202 ·Status: COMPLETED ·Phase: NA
-
Feasibility of Aerodigestive Stimulation Therapy Trial
NCT06118697 ·Status: RECRUITING ·Phase: NA
-
Effect of Teduglutide on Gastric Emptying in Healthy Subjects
NCT01209351 ·Status: COMPLETED ·Phase: PHASE1
-
Short Bowel Syndrome Research Study for Children Up To 17 Years of Age on Parenteral Nutrition
NCT02682381 ·Status: COMPLETED ·Phase: PHASE3
-
REgulatory T Cell infuSion fOr Lung Injury Due to COVID-19 PnEumonia
NCT04468971 ·Status: COMPLETED ·Phase: PHASE1
-
Amoxicillin for Enteral Nutrition Intolerance in Pediatric Intensive Care Unit
NCT05828758 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Pilot Study to Investigate the Effect of Teduglutide on Temporary Ileostomy Function and Complications
NCT03953170 ·Status: WITHDRAWN ·Phase: PHASE3
-
Intravenous Heparin as an Adjunct for the Treatment of Anaphylactic Reactions in an Emergency Department
NCT00657228 ·Status: WITHDRAWN ·Phase: NA
-
The Comparison of Different Administration Routes of Pediatric Premedication
NCT02313337 ·Status: UNKNOWN ·Phase: PHASE4
-
Safety and Efficacy Study of Teduglutide in Subjects With Short Bowel Syndrome Who Completed Protocol CL0600-004 (NCT00081458)
NCT00172185 ·Status: COMPLETED ·Phase: PHASE3
-
Feasibility Study to Evaluate Safety of Nutriseal™ Nutriplace™ System
NCT03371160 ·Status: TERMINATED ·Phase: NA
-
PEAnut Anaphylaxis Predictors
NCT02424136 ·Status: COMPLETED ·Phase: NA
-
A Pharmacokinetic, Safety, and Pharmacodynamic Study of Teduglutide in Pediatric Subjects With Short Bowel Syndrome
NCT01952080 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of the Algorithm for Enteral Nutrition Support
NCT04609358 ·Status: COMPLETED ·Phase: NA
-
Quality of Life in Patients With Short Bowel Syndrome Treated Without and With Teduglutide - a Prospective Nested Matched Pair Analysis
NCT04733066 ·Status: UNKNOWN
-
Steroid Use in Treatment of Allergic Reactions to Food
NCT07341776 ·Status: RECRUITING ·Phase: PHASE4
-
Dexamethasone Use in Pediatric Rhabdomyolysis Patients in Addition to Standard Protocols
NCT06429982 ·Status: RECRUITING ·Phase: PHASE1
-
Neuromuscular Electrical Stimulation for Children With Dysphagia
NCT06309056 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
1-hour Premedication for Allergy Goal in Emergency: PAGE-1 Study
NCT07268248 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Timing of Initiation of Parenteral Nutrition for Critically Ill Children
NCT04693143 ·Status: UNKNOWN ·Phase: NA
-
A Study to Evaluate the Incidence of Hypersensitivity After Administration of Sugammadex in Healthy Participants (MK-8616-101)
NCT02028065 ·Status: COMPLETED ·Phase: PHASE1
-
Feeding Children Nasogastrically Versus Nasojejunally While Receiving Noninvasive Positive Pressure Ventilation
NCT01301352 ·Status: COMPLETED ·Phase: NA
-
Effects and Safety of Infusion of Low-Doses of Methylprednisolone in Early ALI and ARDS in Children
NCT01757899 ·Status: WITHDRAWN ·Phase: PHASE2