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Hypersensitivity clinical trials

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NCT ID: NCT02731833 Completed - Dentin Sensitivity Clinical Trials

Short Term Clinical Study Investigating the Efficacy of an Occluding Dentifrice in Providing Relief From Dentinal Hypersensitivity

Start date: April 2016
Phase: Phase 4
Study type: Interventional

This single centre, comparative design study will be used to investigate the efficacy of an experimental stannous fluoride containing dentifrice in relieving dentinal hypersensitivity (DH) after short term use compared with a standard fluoride dentifrice

NCT ID: NCT02721290 Recruiting - Regional Anesthesia Clinical Trials

Comparison of the Sensitive Cutaneous Block Distribution Following Femoral Nerve Block Using Two Femoral Block Techniques

Start date: January 2016
Phase: N/A
Study type: Interventional

In this study, we will be comparing two approaches to the femoral block. The first or classical approach and one that is the most popular in our institution is used by combining ultrasound guidance and neurostimulator to do the block. The second is performed with the ultrasound alone aiming at the inferolateral aspect of the femoral artery with the needle and injecting. The primary endpoint of the study is the sensitive cutaneous block distribution using both techniques.

NCT ID: NCT02719405 Terminated - Milk Allergy Clinical Trials

Impact of Infant Formula on Resolution of Cow's Milk Allergy

Start date: February 2016
Phase: Phase 2
Study type: Interventional

Primary Endpoint -The percentage of subjects who develop tolerance to cow's milk protein by 12 months post randomization to study formula. Secondary Endpoints - Tolerance - The transcriptional profile of milk-specific T cells by clinical outcome. - Growth and Weight Velocity - Stool Consistency and Frequency - The estimated frequency of milk-specific T cells by clinical outcome. - The TCR diversity of milk-specific T cells by clinical outcome. - The milk allergen component-specific IgE, IgG4 and IgA by clinical outcome. - Safety - The rate of reported adverse events by treatment group.

NCT ID: NCT02711163 Completed - Cow Milk Allergy Clinical Trials

Evaluation of the Hypoallergenicity of an Extensively Hydrolyzed Formula

ALYCE
Start date: April 2016
Phase: Phase 3
Study type: Interventional

The aim of this study is to assess the hypoallergenicity of a new thickened extensively hydrolyzed formula, in infants with confirmed cow's milk protein allergy assessed through a double blind placebo controlled food challenge, followed by a 3-month open feeding period.

NCT ID: NCT02710136 Completed - Asthma Clinical Trials

Cockroach Nasal Allergen Challenge Pilot

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

This research is being done to look at the body's response to cockroach extract, an allergen, when sprayed into the nose. The spraying of the cockroach extract into the participant's nose is called Nasal Allergen Challenge (NAC). The purpose of this study is to evaluate the safety and tolerability of a intranasal cockroach extract given to participants with asthma.

NCT ID: NCT02705716 Completed - Dentin Sensitivity Clinical Trials

Study Investigating Efficacy of an Occluding Dentifrice for Dentine Hypersensitivity

Start date: March 1, 2016
Phase: N/A
Study type: Interventional

This study will investigate the efficacy of an experimental dentifrice containing 0.454% weight/weight (w/w) stannous fluoride in relieving dentine hypersensitivity (DH) after twice daily brushing, over a 2 week treatment period compared with a standard fluoride dentifrice.

NCT ID: NCT02702349 Not yet recruiting - Penicillin Allergy Clinical Trials

The Frequency of Positive Challenge Test to Penicillin in Children Suspected to Have Allergy to Penicillin

Start date: April 2016
Phase: N/A
Study type: Interventional

The incidence of reactions during penicillin challenge tests among children with suspected penicillin allergy

NCT ID: NCT02690935 Completed - Seasonal Allergy Clinical Trials

Efficacy of 2LALERG (Homeopathic Drug) in Allergic Rhinitis Related to Grass Pollen

LLB-2016-01
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to demonstrate the superiority of 2L®ALERG over placebo in terms of efficacy on the symptoms of allergic rhinitis and allergic rhinoconjunctivitis in patients with seasonal allergy to grass pollen, corrected according to rescue medication intake. The secondary objectives are to compare the allergy symptoms, the rescue medication intake, the quality of life and the safety in patients treated with 2L®ALERG or with a placebo. This is a multicentre, randomized, double-blind, two-parallel group, interventional placebo-controlled study with a notified homeopathic medication, marketed since 2002. Fifty patients will be recruited per group to achieve 40 cases completed per group, i.e., a total of 100 patients included for 80 cases completed. Screening will be done before the peak of pollination and the treatment will be set up two months before traditional pollen peak, then visits at 3 months and 6 months, or end of the peak. The treatment will consist of 1 capsule daily, fasting morning, following the numerical order of 1 to 10 capsules for 6 months. The placebo will have the same form, colour, taste and aspect. The allowed concomitant treatments are the already established treatments for associated pathologies not liable to have an impact on the proper conduct of the study and the rescue medications allowed in the first-line adjuvant treatment (oral or topical antihistamines [nasal or eye] and eye cromoglycate, topical nasal corticosteroids [in case of failure or insufficiency of those above]). The prohibited treatments are the oral or injectable corticosteroids and the anti-leukotrienes.

NCT ID: NCT02686996 Recruiting - Insulin Sensitivity Clinical Trials

The Potential of Carnosine Supplementation in Reducing the Cardiometabolic Risk

Start date: February 13, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether carnosine supplementation in overweight/obese individuals can improve insulin secretion and/or insulin resistance by decreasing sub clinical inflammation. The investigators hypothesise that carnosine supplementation will reduce type 2 diabetes and cardiovascular risk factors by lowering chronic low-grade inflammation (CLI), oxidative stress, advanced glycation end products (AGEs), and advanced lipoxidation end products (ALEs). Aim :To determine the capacity of carnosine supplementation to decrease major risk factors for type 2 diabetes and cardiovascular disease and identify metabolic pathways involved, specifically by: 1. Reducing diabetes risk (insulin sensitivity; secretory function and glucose tolerance) 2. Improving cardiovascular risk factors (lipids; arterial (aortic) stiffness; central blood pressure (cBP); endothelial function). 3. Decreasing the CLI, oxidative stress, AGEs, and ALEs, and increase detoxification of reactive carbonyl species (RCSs).

NCT ID: NCT02686827 Completed - Hypersensitivity Clinical Trials

DBPC-Dose-finding-trial of Vitamin D3 for SCIT in Birch Pollen Allergic Patients.

BM4SIT
Start date: October 2015
Phase: Phase 2
Study type: Interventional

Low Vitamin D3 (VD3) levels have been reported to be associated with the risk of allergic diseases like asthma. VD3 has been demonstrated in vitro, ex vivo and in animal models to program the immune system towards anti-inflammatory immune responses. VD3 co-administered with allergen may be a promising adjuvant to improve the onset and efficacy of allergen immunotherapy (AIT). A clinical trial will be performed to compare the immune effects, the tolerability and safety of multiple doses of aVD3 analogue (registered for the intravenous route) administered by the subcutaneous (s.c.) route in subjects with allergic rhinitis and healthy controls. The overall aim is to provide additional (in vivo) support for the use of VD3 as an adjuvant in allergen-specific immunotherapy, on top of the existing pre-clinical evidence demonstrating that antigen-presenting cells educate the adaptive immune system towards an anti-inflammatory response when allergen is seen in the presence of VD3.