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Hypersensitivity clinical trials

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NCT ID: NCT04397029 Terminated - Breast Cancer Clinical Trials

Assessing the Sensitivity of "SureTouchâ„¢" in Women Undergoing Diagnostic and Screening Mammography

Start date: January 4, 2019
Phase: N/A
Study type: Interventional

Prospective, case-control study being conducted to determine the sensitivity of the SureTouch device in detecting known masses at a pre-determined level of specificity.

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: NCT04377087 Terminated - Ovarian Cancer Clinical Trials

Delayed Initiation of Olaparib Maintenance Therapy in Platinum Sensitive Recurrent Ovarian Cancer

Start date: June 29, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test if delaying the start of the olaparib until there is a rise in a tumor marker called CA-125 will result in a longer time until the next or different treatment for the patient's cancer. The study will also evaluate how delaying the start of maintenance therapy will affect symptoms; physical functioning; quality of life; and impact on finances.

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: NCT04376242 Recruiting - Food Allergy Clinical Trials

Virtual Reality Technology Versus Standard Technology During Pediatric Oral Food Challenge

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if non-invasive distracting devices (Virtual Reality headset) are more effective than the standard of care of utilizing existing technologies that are currently more common in food allergy research treatment and clinics (i.e. television and patients' personal electronic devices) for decreasing levels anxiety and fear in pediatric patients undergoing oral food challenge (OFC) and their caregivers.

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: NCT04361370 Enrolling by invitation - Clinical trials for Platinum-sensitive Recurrent BRCA Wild Type Ovarian Cancer

Olaparib Maintenance With Pembrolizumab & Bevacizumab in BRCA Non-mutated Patients With Platinum-sensitive Recurrent Ovarian Cancer

OPEB-01
Start date: October 28, 2020
Phase: Phase 2
Study type: Interventional

This study is phase II, open label, clinical trial to determine the efficacy of Olaparib maintenance with Bevacizumab and Pembrolizumab by assessment progression-free survival(6 months PFS rate) in BRCA non-mutated patients with platinum-sensitive recurrent ovarian cancer.

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.