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Hypersensitivity clinical trials

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NCT ID: NCT03457337 Recruiting - Clinical trials for Advanced NSCLC With EGFR Mutation

S-1 Plus Gefitinib Versus Gefitinib Monotherapy in Patients With EGFR-sensitive Mutation Advanced Non-squamous NSCLC

Start date: March 28, 2018
Phase: Phase 2
Study type: Interventional

To investigate the survival benefit of first-line therapy for patients with EGFR-sensitive mutation-positive advanced non-squamous non-small cell lung cancer treated with S-1plus gefitinib versus gefitinib monotherapy

NCT ID: NCT03456479 Not yet recruiting - Cow Milk Allergy Clinical Trials

Diagnosis of Cow's Milk Protein Allergy Among Infants and Children in Assuit University Children Hospital

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The study will assess the diagnosis of Cow's milk protein allergy (CMPA) among infant and children in Assiut University Children Hospital using skin prick test and specific serum IgE

NCT ID: NCT03453307 Recruiting - NSCLC Clinical Trials

Drug Sensitivity Correlation Between Patient-Derived Organoid Model and Clinical Response in NSCLC Patients

Start date: January 30, 2018
Phase: N/A
Study type: Observational

This clinical study aims to evaluate the feasibility to predict clinical response of target therapy or chemotherapy drugs based on the ex vivo drug sensitivity data using patient-derived organoids.

NCT ID: NCT03449537 Completed - Allergy Milk Clinical Trials

Step Down Approach in Children With Cow Milk Allergy

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

Cow's milk allergy (CMA) affects up to 3% of European children. In the absence of an alternative to cow's milk, the management of CMA is based on the use of safe, affordable and nutritionally adequate formulas. In Scientific Societies Guidelines, extensively hydrolyzed casein formula (EHCF) is considered as safe first line approach for the treatment of children with CMA, whereas amino acid-based formula (AAF) is considered as second line strategy in children reacting to EHCF or as first line approach in children with CMA-induced anaphylaxis. Few and not recent studies, involving a poorly characterized study population, suggested that up to 10% of CMA children could react to the extensively hydrolysed formulas. It has been demonstrated that EHCF supplemented with L.rhamnosus GG (LGG) maintains hypoallergenic status and that is able to accelerate oral tolerance acquisition in children with CMA comparing with other formulas. The purpose of this study is to investigate the feasibility of a "step-down" approach in children affected by Immunoglobulin E (IgE)-mediated CMA with the aim to evaluate the effects of EHCF + LGG on oral tolerance acquisition and on immune response and gut microbiota shaping.

NCT ID: NCT03446053 Completed - Healthy Volunteers Clinical Trials

A Study to Evaluate the Safety, PK, PD, Immunogenicity of N-Rephasin® SAL200 in Healthy Male Volunteers

Start date: February 7, 2018
Phase: Phase 1
Study type: Interventional

To evaluate the safety, pharmacokinetics, pharmacodynamics and immunogenicity of N-Rephasin® SAL200 following single and multiple ascending doses in healthy male volunteers after continuous intravenous infusion over 60 minutes.

NCT ID: NCT03441438 Recruiting - Clinical trials for Aspirin-Sensitive Asthma With Nasal Polyps

Mechanisms of Alcohol Sensitivity in AERD

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

The purpose of this study is to determine what type of reactions in the body may be responsible for the respiratory symptoms that occur when patients with Aspirin Exacerbated Respiratory Disease (AERD) drink alcoholic beverages. These reactions are most often seen with red wine.

NCT ID: NCT03439202 Completed - Clinical trials for Heart Rate Variability

Low Intensity Exercise in Different Normobaric/Hypobaric Normoxic/Hypoxic Conditions.

Hypoxia
Start date: March 19, 2018
Phase: N/A
Study type: Interventional

The main goal of this project is to investigate how low intensity cycling exercise (1.5W/kg, for 6 minutes) influences cerebral functions, such as: Cerebral blood flow, oxygenation, and other physiological variables in different normobaric and hypobaric hypoxic conditions.

NCT ID: NCT03434782 Completed - Dentin Sensitivity Clinical Trials

Effect of Laser and Potassium Nitrate Application on the Sensitivity Control in Bleached Teeth

Start date: April 24, 2017
Phase: Phase 1
Study type: Interventional

To investigate the effects of desensitizing agents on the dental bleaching process, testing the hypothesis that they may control dental sensitivity.

NCT ID: NCT03427021 Terminated - Clinical trials for GI Patients on Oxaliplatin Containing Regimen

A Randomized Study to Establish the Efficacy of Oral Ice Exposure During Oxaliplatin Infusion in Preventing Oral Cold Sensitivity

Start date: February 1, 2017
Phase: Early Phase 1
Study type: Interventional

The main purpose of this study is to evaluate whether exposure to ice chips in the mouth (oral ice chips) during oxaliplatin treatment prevents or reduces symptoms of cold sensitivity.

NCT ID: NCT03413995 Active, not recruiting - Clinical trials for Prostate Cancer Metastatic

Trial of Rucaparib in Patients With Metastatic Hormone-Sensitive Prostate Cancer Harboring Germline DNA Repair Gene Mutations

TRIUMPH
Start date: September 10, 2018
Phase: Phase 2
Study type: Interventional

The aim of this research is to find out if the study drug rucaparib leads to lowering of PSA levels in men with metastatic prostate cancer that has not yet been treated with androgen deprivation therapy (also referred to as metastatic hormone sensitive prostate cancer) and who have an inherited mutation in a gene involved in repairing DNA damage. The research will also examine if rucaparib is safe in individuals with metastatic prostate cancer. Prior research studies have shown that drugs like rucaparib can be of benefit to patients with advanced metastatic prostate cancer who are resistant to androgen deprivation therapy AND who carry a mutation in a DNA repair gene. We are studying if rucaparib will be an effective treatment for these patients earlier in their treatment course (for example, prior to the start of medicines that lower testosterone level). It is unknown whether rucaparib will have the same benefit in men with metastatic prostate cancer carrying a mutation in a DNA repair gene, prior to the use of medicines that lower your testosterone level.