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Blister clinical trials

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NCT ID: NCT02343783 Completed - Healthy Clinical Trials

A Study to Evaluate Use of Induced Skin Blisters in Adult Participants With Atopic Dermatitis, Allergic Asthma and Atopic Healthy Participants

Start date: January 2015
Phase: Phase 0
Study type: Interventional

The purpose of this study is to characterize the cell (the basic building block of all living things) populations and inflammatory (pain and swelling) mediator responses in suction skin blister fluid after allergic skin reaction (ASR) [rash] induction with D. Pteronyssinus [house dust mite (HDM)], Alternaria alternata, or Aspergillus fumigatus allergens in participants with atopic dermatitis (AD) [Skin rash, Eczema] or allergic asthma (AA) [breathing disorder in which there is a wheezing and difficulty breathing].

NCT ID: NCT02058641 Completed - Atherosclerosis Clinical Trials

Effect of Darapladib on Cantharidin-Induced Inflammatory Blisters in Subjects With Type 2 Diabetes Mellitus (T2DM)

Start date: February 26, 2014
Phase: Phase 1
Study type: Interventional

This will be an exploratory, open-label, single sequence, two part study (Part A and an optional Part B). The aim of this study will be to assess whether systemic inhibition of Lipoprotein associated phospholipase A2 (Lp-PLA2) in humans, effected by 11 days of once daily dosing to steady state with 160 milligrams (mg) of enteric coated (EC) darapladib, will specifically reduce the number of macrophages and/or result in a higher proportion of M2 macrophages in skin blisters induced by cantharidin (a chemical agent that causes blisters). In Part A of the study, a cohort of 8 subjects with type 2 diabetes mellitus will be recruited. In Part B of the study, a cohort of 8 additional healthy subjects with matching age (+/- 24 months) and gender to Part A may be recruited.

NCT ID: NCT01945112 Completed - Blister of Foot Clinical Trials

Prevention Trial Assessing Paper-Tape in Endurance Distances II (Pre-TAPED II)

Start date: February 2014
Phase: N/A
Study type: Interventional

Friction foot blisters are one of the most common and often debilitating complaints of all athletes, and hikers and runners in particular. Blistering rates in the literature of outdoor hikers range from 7%-54%. This study's aim is to build on Pre-TAPED I, and determine whether applying paper tape to the areas of the foot where blisters historically occur in endurance runners can prevent the incidence of friction blisters.

NCT ID: NCT01859780 Completed - Clinical trials for Unintentional Ingestion of Prescriptions Within Vials and Blisters

Visual Distraction as a Means of Enhancing Child Resistance

VDCR
Start date: August 2013
Phase: N/A
Study type: Interventional

Unintentional poisonings of children continues to be a major issue in the US. According to a study conducted by Cincinnati Children's Hospital Medical Centers, during the period from 2001-2008, emergency room visits for children less than 5 rose 28% as the result of pharmaceutical products. The authors note, "the problem of pediatric medication poisoning is getting worse, not better." Child resistant closures have been required on most medications sold in the US since the early 1970s. However, most designs attempt to thwart children through purely physical means (e.g. simultaneous dissimilar motion or opening using sequential tasks). Few, if any designs, have utilized perception and cognition as a way to enhance child resistance. The investigators propose utilizing visual illusions in spaces distinct from the opening mechanism of prescription packages as a means of enhancing child resistance. In this project, visual illusion images are applied to both vials and wallet blisters in order to attract children's interest and prolong the time before opening. During Stage I, the investigators will determine if the visual distractor attracts attention when samples are displayed in a storage rack. During Stage II, the investigators will test the effect of visual distractors on child resistance as measured by successful openings and time to open.

NCT ID: NCT01762787 Completed - Inflammation Clinical Trials

Phase I Methodology Study to Validate the Cantharidin Blister Model in Healthy Volunteers

Start date: August 17, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to refine the cantharidin-induced blister assay in healthy volunteers as a model of inflammatory disease. The study is an experimental trial in healthy volunteers in two parts; Part 1 to optimise the model and Part 2 to validate using two anti-inflammatory treatments with different modes of action.

NCT ID: NCT01469871 Completed - Hip Surgery Clinical Trials

Evaluation of Three Types of Dressings After Hip Surgery

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if one of the new types of dressings (MEPORE PRO and/or MEPILEX BORDER ) will reduce the blister rate compared to the currently used HYPAFIX.

NCT ID: NCT01120808 Completed - Blister Clinical Trials

Prevention Trial Assessing Paper-Tape in Endurance Distances (PreTAPED)

Start date: April 2010
Phase: Phase 1
Study type: Interventional

Blisters are a very common complaint in both the general population and also the athlete. This study's aim is to determine whether applying paper tape (an inexpensive and common component of most foot care kits) to the foot of endurance runners prevents the frequency and severity of friction blisters.

NCT ID: NCT01118208 Completed - Clinical trials for Medication Adherence

Blister Packaging Medication to Increase Treatment Adherence and Clinical Response

BP
Start date: September 2009
Phase: N/A
Study type: Interventional

This quantitative, interview-based study will determine if increased prescription medication adherence via blister pack administration will reduce suicide related behavior among the high risk population of patients discharged from a psychiatric inpatient unit. The aims of the project are to determine whether blister packaging medication significantly increases treatment adherence and if blister packaging significantly decreases intentional self-poisoning behavior (i.e., suicide attempts and completions). By tracking former psychiatric inpatients for 12 months post-discharge and obtaining monthly medication adherence ratings, we will determine if blister packaging (BP) medications leads to better adherence than dispensing as usual (DUA). The psychiatric patients we will be recruiting have been diagnosed with, major affective disorder, bipolar affective disorder, post-traumatic stress disorder, or schizophrenia (or any combination of these diagnoses). By tracking former psychiatric patients for 12 months post-discharge and obtaining monthly reports (self-report and medical record review) of suicide-related behaviors, we will determine if patients in the BP condition have less intentional self-poisoning behavior than those in the DAU condition.

NCT ID: NCT01088685 Completed - Blister Clinical Trials

Hydrogel Blister Patch Prototype Treatment for Foot Blisters on the Heel

Start date: March 2010
Phase: N/A
Study type: Interventional

Study to evaluate the safety and performance of a new blister patch intended to treat blisters on the heel of the foot.

NCT ID: NCT01026064 Completed - Inflammation Clinical Trials

Cantharidin-induced Skin Blister for Testing Anti-inflammatory Effects of Macrolides

Start date: June 4, 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the utility of the cantharidin-induced skin blister assay for evaluation of the anti-inflammatory effects of macrolides in healthy male volunteers.