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Hypersensitivity clinical trials

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NCT ID: NCT02257684 Terminated - Clinical trials for Acute Lymphoblastic Leukemia

A Dose Confirmation and Pharmacokinetic Study of Pegcrisantaspase Administered as Intravenous (IV) Infusion in Children and Young Adults With Acute Lymphoblastic Leukemia (ALL) /Lymphoblastic Lymphoma (LBL). Following Hypersensitivity to Pegaspargase (Oncaspar)

Start date: September 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness,safety, and dosage of pegcrisantaspase in patients with Acute Lymphoblastic Leukemia (ALL) / Lymphoblastic Lymphoma (LBL).

NCT ID: NCT02213341 Terminated - Clinical trials for Food Hypersensitivity

Impact of Vaccination on Th2 Immunity in Infancy

Start date: January 2015
Phase:
Study type: Observational

The purpose of this study is to assess the responses in the immune system of infants after they receive the vaccine against diphtheria, tetanus, and pertussis (DTaP). The investigators will do this by studying the immune cells and allergy responses in the blood prior to and after receipt of the third DTaP vaccine.

NCT ID: NCT02185651 Terminated - Pompe Disease Clinical Trials

A Pilot Study of Zavesca® in Patients With Pompe Disease and Infusion Associated Reaction

Start date: October 2016
Phase: Phase 1
Study type: Interventional

Hypothesis: the effectiveness of treatment of Pompe disease with rhGAA enzyme replacement therapy (ERT) is limited at least in part because patients develop antibodies against the provided rhGAA enzyme. Treatment with Zavesca® prior to infusion may dampen or eliminate the anti-rhGAA immune response in patients receiving ERT, thereby allowing for greater ERT efficacy. Treatment with Zavesca® before a enzyme replacement therapy (ERT) may decrease the severity of, or eliminate infusion associated reactions (IAR) in people with Pompe Disease receiving ERT.

NCT ID: NCT02035345 Terminated - Clinical trials for Recurrent Ovarian Cancer

Slowed Carboplatin Infusion for Ovarian Cancer Patients Receiving Carboplatin Re-Treatment

Start date: January 2014
Phase: Phase 4
Study type: Interventional

This is a research study to determine if administering carboplatin at a slower rate when re-treating recurrent ovarian cancer patients prior to the development of a hypersensitivity reaction will decrease the frequency and severity of future hypersensitivity reactions.

NCT ID: NCT02032056 Terminated - Allergy Clinical Trials

Effect of Probiotics in Reducing Infections and Allergies in Young Children During the Complementary Feeding Period

ProbiComp
Start date: September 2013
Phase: N/A
Study type: Interventional

The aim of the intervention is to examine the effect of the bacterial strain BB-12, provided for 6 mo, on the prevalence of infections and allergic manifestations in small children, and how BB-12 affects the immune system, the gastrointestinal tract and the microbiota. Children are enrolled during 2 winter seasons.

NCT ID: NCT01950559 Terminated - Soy Allergy Clinical Trials

Evaluation of Potential Allergenicity of New Soybean Varieties

Monsanto
Start date: September 2013
Phase:
Study type: Observational

Food allergy is on the rise within the pediatric population. Having a food allergy can cause medical, nutritional and psychological issues in those who suffer with it. Although making the appropriate diagnosis of food allergy is very important, properly diagnosing food allergy has been a challenge. Skin prick testing and food-specific immunoglobulin-e (IgE) testing of the blood can give positive results that are false. Currently, Oral Food Challenges are the best way to diagnose a food allergy. Unfortunately, Oral Food Challenges are time consuming and may not be readily available to suspected food allergy sufferers. This study is designed to examine the effectiveness of an allergy-detecting blood test called ImmunoCAP manufactured by the company, ThermoFisher. Soybean is one of the eight allergy-inducing foods that are responsible for 90% of all food allergies. A part of the study is to allow the study Sponsor to use some of the blood sample collected from you to test if genetically-changed soy has more or less allergy producing factors. This is important to the Sponsor to test the safety of their genetically modified soy.

NCT ID: NCT01942486 Terminated - Migraine Disorders Clinical Trials

Thin Film Spectacle Coatings to Reduce Light Sensitivity and Headaches in Child and Adolescent Patients With Migraine

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a special coating, applied to the surface of glasses can reduce the frequency and severity of migraine headaches in children and adolescents. This study is being conducted by researchers at Primary Children's Medical Center, The John Moran Eye Center, and the University of Utah Department of Electrical Engineering. The investigators have determined that a specific frequency of light is particularly bothersome to migraine patients. The coating they've developed is designed to block this frequency of light. Very few treatments are approved for the treatment of childhood migraine. The investigators hope that these glasses will provide a safe way to improve headaches in children.

NCT ID: NCT01897077 Terminated - Peanut Allergy Clinical Trials

The Safety and Efficacy of a Peanut Immunotherapy Dissolving Film for Peanut Allergy

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if a new method of administration of peanut sublingual immunotherapy, a dissolving peanut film, is effective.

NCT ID: NCT01775176 Terminated - Clinical trials for Polycystic Ovary Syndrome

Effect of Weight & Insulin Sensitivity on Reproductive Function in PCOS: Studies in Skeletal Muscle & Adipose

PULSE-A
Start date: May 2012
Phase:
Study type: Observational

The overall objective of this ancillary study is to obtain skeletal muscle and subcutaneous adipose tissue biopsies from women with polycystic ovary syndrome enrolled in the PULSE Study (NCT01482286).

NCT ID: NCT01529242 Terminated - Clinical trials for Cutaneous Hypersensitivity

Comparison of Desloratadine Associated With Prednisolone Oral Solution Versus Dexchlorpheniramine Associated With Betamethasone for Cutaneous Rash Treatment

Start date: February 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the non-inferiority clinical efficacy of two different drug associations in the treatment of acute cutaneous rash in children between 2 and 12 years old.