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Hypersensitivity clinical trials

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NCT ID: NCT02414243 Completed - Cow's Milk Allergy Clinical Trials

Study to Assess Hypoallergenicity of a New Amino-acid Based Infant Formula in Children With Cow's Milk Allergy

RAF
Start date: April 2015
Phase: N/A
Study type: Interventional

This is a prospective, controlled, multi-country study to verifying the hypoallergenicity of the new amino acid-based formula in infants and children aged< 12 years with documented cow's milk protein allergy (CMPA).

NCT ID: NCT02412813 Withdrawn - Clinical trials for Total Knee Replacement Revision

LEGION™ Revision Metal Hypersensitivity Study

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

This is a prospective, randomized, multi-center, metal hypersensitivity study comparing OXINIUM and cobalt chrome femoral components in subjects with failed total knee arthroplasty (TKA).

NCT ID: NCT02411344 Completed - Clinical trials for Endocrine Sensitive HER2+/HR+ Breast Cancer

Preoperative Study With Trastuzumab, Pertuzumab and Letrozole in Breast Cancer Patients Sensitive to Hormonal Therapy

PER-ELISA
Start date: February 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the activity of molecular response in endocrine sensitive breast cancer HER2+/HR+ patients treated with Pertuzumab-trastuzumab plus Ietrozole.

NCT ID: NCT02406573 Completed - Dentin Sensitivity Clinical Trials

A Pilot Study to Assess Nominal Versus Controlled Stimuli on Dentinal Hypersensitivity

Start date: March 2015
Phase: N/A
Study type: Interventional

This pilot study will evaluate the use of nominal stimuli to assess dentinal hypersensitivity response relative to a clinically-controlled stimulus.

NCT ID: NCT02405923 Terminated - Cow's Milk Allergy Clinical Trials

Growth, Safety and Tolerance of a Rice Protein Hydrolysate Formula in Infants With Cow's Milk Protein Allergy

GRITO-14
Start date: July 1, 2014
Phase: N/A
Study type: Interventional

This is a multicenter, controlled, randomized, prospective, non-inferiority, double blind intervention trial to evaluate the children growth (at 6, 9 and 12 months) using a rice hydrolysed protein formula compared to an extensively cow's milk protein hydrolysed formula for the management of Cow's Milk Protein Allergy (CMPA).

NCT ID: NCT02402231 Active, not recruiting - Peanut Allergy Clinical Trials

Treatment of Severe Peanut Allergy With Xolair (Omalizumab) and Oral Immunotherapy

FASTX
Start date: October 2013
Phase: Phase 2
Study type: Interventional

Severe peanut allergy is different from other allergic reactions because it can lead to fatal reactions and is an invisible disability. There is no cure today. The purpose of this study is to treat children and adolescents with severe peanut allergy with oral immunotherapy with peanuts under the protection of anti-IgE (immunoglobulin E) antibodies (omalizumab), and thereby inducing tolerance to peanuts. The treatment will be monitored by basophil cell stimulation (CD-sens).

NCT ID: NCT02397876 Completed - Food Allergy Clinical Trials

Partially Hydrolyzed Whey Formula in Cow's Milk Allergic Patients

Start date: March 2015
Phase: N/A
Study type: Interventional

Cow's milk (CM) allergy is the most common food allergy in children, affecting 2-3% of infants. In formula-fed infants with CM allergy, extensively hydrolyzed or amino acid-based infant formulas are typically recommended. These formulas are expensive and not palatable. For older patients with CM allergy, the standard of care is avoidance of all CM products. The investigators cared for a CM allergic patient who was able to tolerate partially hydrolyzed whey formula (pHWF), which tastes better and is less expensive than extensively hydrolyzed or amino-acid based formulas. There are likely other subjects who could similarly tolerate pHWF. Furthermore, it is possible that taking pHWF could accelerate tolerance of CM. The investigators aim to identify characteristics of CM allergic subjects who can tolerate pHWF and assess the degree to which taking pHWF accelerates CM tolerance.

NCT ID: NCT02397447 Completed - Clinical trials for Diabetes Mellitus Type 2

Effect of Momordica Charantia Administration on Type 2 Diabetes Mellitus, Insulin Sensitivity and Insulin Secretion

Start date: March 2013
Phase: Phase 2
Study type: Interventional

The hypoglycemic effect of Momordica Charantia has been evaluated in clinical trials in patients with type 2 diabetes mellitus. Important reductions in fasting plasma glucose, glycated hemoglobin (A1C), and fructosamine were observed. It is unknown whether this improvement is due to an improvement in insulin sensitivity and insulin secretion. The purpose of this study is to evaluate the effect of the administration of Momordica Charantia on insulin sensitivity and insulin secretion in patients with type 2 diabetes mellitus.

NCT ID: NCT02394015 Completed - Clinical trials for Ovarian Epithelial Cancer Recurrent

Retrospective Study to Analyze the Efficacy and Safety of Trabectedin and Pegylated Liposomal Doxorubicin (PLD ) in the Treatment of Patients With Platinum-sensitive Recurrent Ovarian Cancer (ROC), According to SmPC

RETRO-ROC
Start date: May 6, 2013
Phase:
Study type: Observational

Retrospective Study to Analyze the Efficacy and Safety of Trabectedin and Pegylated Liposomal Doxorubicin (PLD ) in the Treatment of Patients With Platinum-sensitive Recurrent Ovarian Cancer (ROC), According to SmPC.

NCT ID: NCT02384044 Completed - Dentin Sensitivity Clinical Trials

A Pilot Clinical Study to Evaluate the Safety and Efficacy of Marketed Oxalate Strips Compared to a Marketed Safety Pen

Start date: February 2015
Phase: N/A
Study type: Interventional

This pilot study will evaluate the safety and effectiveness of a marketed sensitivity strip on existing dentinal hypersensitivity compared to a marketed sensitivity pen.