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Hypersensitivity clinical trials

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NCT ID: NCT04421638 Completed - Clinical trials for Drug Hypersensitivity

Cephalosporin Hypersensitivity

CephALL
Start date: January 30, 2020
Phase:
Study type: Observational

Background : Although the hypersensitivity reactions to cephalosporins have been recently a more focused subject, studies on the cephalosporin as an allergen are significantly less frequent that those regarding penicillins. Most of the available data regards cephalosporin sensitization in patients previously allergic to penicillin. Like penicillins, cephalosporins represent one of the most prescribed classes of antibiotics. The diagnosis of cephalosporin hypersensitivity is based mainly on clinical history, skin tests (ST) and drug provocation tests (DPT). This succession of tests, performed in specialized services, allows to eliminate responsibility for the drug in many cases (80-85%). The drug allergy work-up also allows to identify profiles of allergy to cephalosporins, with different patterns of cross-reactivity. Objective: To analyse the characteristics of patients studied in our Unit for suspicion of cephalosporin hypersensitivity. Methods: This retrospective study will comprise all the patients who attended the allergy service of the UH of Montpellier from 1997 till 2018 with a clinical history evocative of cephalosporin drug hypersensitivity reaction (DHR), who underwent a drug allergy work up and who gave their consent to be included in the study . The Patients are selected from the Drug Allergy & Hypersensitivity Database (DAHD).

NCT ID: NCT04404907 Completed - Sun Sensitivity Clinical Trials

Deliberate Ultraviolet Light Exposure to Get a Tan by Young Adult Sexual Minority Males

Start date: July 15, 2019
Phase:
Study type: Observational

The purpose of this study is to: a) identify enablers and barriers to deliberate ultraviolet light exposure by young sexual minority men (SMM), and b) quantify the extent of their deliberate ultraviolet light exposure.

NCT ID: NCT04401956 Completed - Clinical trials for Non-celiac Gluten Sensitivity

Bread Study: Comparison of the Tolerance of Spelt and Wheat Bread

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

This project aims to verify the hypothesis that spelt products are more tolerable than bread wheat products in a target group of individuals with self-diagnosed wheat sensitivity. In addition, the influence of different manufacturing processes will be considered.

NCT ID: NCT04400214 Completed - Child, Only Clinical Trials

The Food Allergy Superheroes Training (FAST) Program

FAST Program
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Among children with a food allergy, strict avoidance (e.g., elimination of allergenic foods from one's diet) is the only intervention capable of preventing potentially devastating health-related sequelae including anaphylaxis and death. Youths from low-income backgrounds are particularly impacted by food allergies and may be the population most apt to benefit from a brief, portable, and engaging skills-based intervention designed to teach young children the skills needed to remain adherent to food allergy safety guidelines. Data collected as part of the proposed project will lay the groundwork for a line of federally-funded intervention research broadly examining how to promote adherence to food allergy safety guidelines among young children from low-income backgrounds through implementation of a robust, efficient, and portable intervention.

NCT ID: NCT04383340 Completed - Premature Birth Clinical Trials

Sensitivity Training for Parents With Premature Infants

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

This study evaluated the effectiveness of a culturally adapted version of the Mother-Infant Transaction Program (MITP) among Chinese mothers with premature infants in public hospitals in Hong Kong.

NCT ID: NCT04378335 Completed - Clinical trials for Food Allergy in Children

Assessment of Orality Disorders in Children With Food Allergies

ALLERGORAL
Start date: October 21, 2020
Phase: N/A
Study type: Interventional

Orality disorders are frequent in child. There are complications like growth and psychomotor development disorders. The aim is to estimate the prevalence of orality disorder for child with one or several food allergy.

NCT ID: NCT04377061 Completed - Anemia Clinical Trials

Anemia in Non-celiac Wheat Sensitivity

Start date: January 1, 2020
Phase:
Study type: Observational

In recent years, a new gluten- or wheat-related disease has emerged, a condition labelled "non-celiac gluten sensitivity" (NCGS) or "non-celiac wheat sensitivity" (NCWS). This is very often a self-reported condition, since patients refer to intestinal [mainly irritable bowel syndrome (IBS)-like] and/or extra-intestinal symptoms (i.e. fatigue, headache, anemia) caused by gluten or wheat ingestion, even though they do not suffer from celiac disease (CD) or wheat allergy (WA). Among the extra-intestinal symptoms, several studies have shown, in patients with NCWS, the presence of anemia, generally mild, often with iron or folate deficiency characteristics, but no research has ever been planned with the specific intention of analyze this particular aspect of the disease. Therefore, the aim of the present multicentric research was to analyze, both retrospectively and prospectively, the laboratory data of NCWS patients, compared to CD and IBS controls, to identify: a) the presence, severity and morphologic characteristic of anemia; 2) possible pathogenic mechanisms.

NCT ID: NCT04367324 Completed - Clinical trials for Low-level Laser Therapy

Effect of Low-Level Laser Therapy Following Direct Pulp Capping on Postoperative Sensitivity by Thermal Stimulus

Start date: October 1, 2017
Phase:
Study type: Observational

The aim of this study was to investigate the effect of low-level laser therapy (LLLT) on postoperative pain provoked by thermal stimulation in direct pulp capping. All the patients who received consent form in this retrospective study were retrieved from the records of patients attended for routine dental treatment at the Ordu University, Faculty of Dentistry, Department of Endodontics between 01.10.2017-01.10.2018. Study subjects were recruited from the pool of patients who performed direct pulp capping by a single operator. A total of 123 pre-treated teeth of 123 patients who referred to Ordu University, Faculty of Dentistry were examined. Follow-up examinations were carried out at postoperative 6th hours, 1st and 7th days with visual analog scale (VAS), and treatment outcome were assessed. Participants were allocated to the laser and control group which consist of 42 patients in each group. 6 patients were excluded from the study due to missing data in both groups. Thus, data from 72 patients who had been carried out direct pulp capping were assessed.

NCT ID: NCT04359368 Completed - Iron-deficiency Clinical Trials

Characteristics of Patients With Hypersensitivity Reactions to Intravenous Iron Infusions

Start date: September 1, 2019
Phase:
Study type: Observational

This study aims to evaluate characteristics of patients with previous hypersensitivity reaction grades I-IV to intravenous ferric carboxymaltose (Ferinject) or to iron sucrose (Venofer) including age, atopy status, previous allergic reactions, previous medical history, current medications and co-morbidities. Furthermore, symptoms on reaction such as severity grade of reaction will be evaluated.

NCT ID: NCT04356911 Completed - Dentin Sensitivity Clinical Trials

The Strontium Chloride Associated With Photobiomodulation in the Control of Post-bleaching Sensitivity

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

This study investigated the effects of the association of strontium chloride with photobiomodulation on the dental bleaching process, testing the hypothesis that they may control dental sensitivity post-bleaching teeth.