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Hypersensitivity clinical trials

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NCT ID: NCT01587950 Completed - Dental Pain Clinical Trials

The Effects of Potassium Nitrate in Reducing Dentinal Hypersensitivity

Start date: February 2009
Phase: Phase 1
Study type: Interventional

A randomized, controlled, double blind exploratory study to explore the effects of two different potassium nitrate concentrations and water on exposed dentine in reducing dentinal hypersensitivity. Solutions will be applied for either 2, 5 or 10 minutes and assessed by visual analogue scale (VAS) scores following evaporative (air) stimulus.

NCT ID: NCT01583907 Recruiting - Food Allergy Clinical Trials

Nutrition in Children With Food Allergy

Start date: March 2012
Phase: Phase 0
Study type: Observational

The investigators aim to asses the effect of dieto-therapy and of nutritional counseling on the nutritional status, body growth and tolerance acquisition in children with cow's milk allergy.

NCT ID: NCT01571830 Completed - Food Allergy Clinical Trials

Improving Nutrient Intake and Growth in Children With Multiple Food Allergies

Start date: December 2011
Phase: N/A
Study type: Observational

- Hypothesis 1: Food allergies are associated with poor growth which can be corrected with nutrition intervention. - More than 10% of children with multiple food allergies will have a weight-for-age z-score less than - 2 at diagnosis. The z-score is a measure of the distance from the mean value, or 50th percentile on the growth chart. A z-score of less than - 2 indicates that the child is underweight. - Growth parameters of children with multiple food allergies will improve after intervention by a team that includes a dietitian and an allergist. - Hypothesis 2: Food allergies are associated with low micronutrient intake which can be corrected with nutrition intervention. o More than 30% of children with multiple food allergies will consume less than 67% of the Dietary Reference Intake for at least one macronutrient or micronutrient at diagnosis. - Macronutrient and micronutrient intake will increase after intervention by a team that includes a dietitian and an allergist. • Hypothesis 3: Food allergies are related to behavioral feeding problems which can be corrected with nutrition intervention. - At least 25% of children with multiple food allergies will have behavioral feeding problems at diagnosis. - Prevalence of behavioral feeding problems will decrease after nutrition intervention.

NCT ID: NCT01569776 Completed - Clinical trials for Food Hypersensitivity

Elemental Formula Hypoallergenicity

Start date: April 2012
Phase: N/A
Study type: Interventional

The primary objective of this clinical trial is to determine whether a new amino acid-based formula is hypoallergenic as defined by the American Academy of Pediatrics (2000), demonstrating that the test formula does not provoke allergenic activity in 90% of infants or children with confirmed cow's milk allergy (CMA) with 95% confidence as compared to a commercially available hypoallergenic formula.

NCT ID: NCT01569191 Completed - Hypersensitivity Clinical Trials

Non-Pharmaceutical Treatment of Seasonal Allergic Conjunctivitis

Start date: March 2012
Phase: Phase 4
Study type: Interventional

Seasonal allergic conjunctivitis (SAC) is an irritating eye condition that affects many people, caused by hypersensitivity to normally harmless substances such as pollen, and often accompanies seasonal hay fever. Treatments that can be used before initiating medical therapy include artificial tear supplements (ATS) and cold compresses (CC). However, there is no evidence in the scientific literature that demonstrates their efficacy compared to no treatment or their combined effect with anti-allergic medication. Therefore the investigators aim to examine the efficacy of ATS and CC alone, in comparison to anti-allergic medication, and CC in combination with anti-allergic medication. In addition, the investigators also aim to determine the time course of ocular allergic reactions. At the end of the study the investigators will be able to see whether or not ATS and CC are effective in treating SAC.

NCT ID: NCT01546753 Completed - Tree Nut Allergy Clinical Trials

Walnut Oral Immunotherapy for Tree Nut Allergy

WOIT
Start date: April 27, 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if walnut oral immunotherapy can be used in participants allergic to tree nuts to reduce tree nut allergy and induce changes in the participant's immune system.

NCT ID: NCT01538979 Completed - Clinical trials for Grass Pollen Allergy

Phase II Study of Grass Pollen Allergy Vaccine BM32

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The study will evaluate the efficacy and safety of BM32 in grass pollen allergic subjects. It will test the hypothesis that either of two doses of BM32 will lead to a sustained relief off allergy symptoms over a two year study period.

NCT ID: NCT01533220 Completed - Flu Clinical Trials

Efficacy of Nasal Naphazoline Hydrocloride + Pheniramine Maleate + Panthenol Compared With Naphazoline Hydrocloride in the Symptomatic Control of Nasal Congestion and Nasopharyngeal

Start date: January 1, 2013
Phase: Phase 3
Study type: Interventional

The common cold is a major cause of nasal obstruction and reaches children and adults two or more times a year. At the moment, there is no cure for the common cold, and therefore the reduction of symptoms is the focus of the treatment. The study has parallel distribution design, with two equal groups, in which one group will be treated by a combination of naphazoline hydrocloride + pheniramine maleate + panthenol and the other will receive treatment with naphazoline hydrocloride.

NCT ID: NCT01529437 Completed - Asthma Clinical Trials

Sublingual Immunotherapy Studies for Grass and Dust Mite Allergies

SLIT
Start date: January 2005
Phase: Phase 1
Study type: Interventional

This is a study for children and adults who are interested in a new therapy for their allergies to dust mite and timothy grass. The new therapy is called sublingual immunotherapy and the investigators are testing if it is safe and well tolerated.

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.