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Blister clinical trials

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NCT ID: NCT04236817 Completed - Clinical trials for Medication Adherence

Impact on Patient COmpliance With Medication Using Pre-packaged Blisters for Long-term Medical therapY

I-COMPLY
Start date: January 1, 2015
Phase: N/A
Study type: Interventional

The use of packaging interventions like pillboxes or blister packs has been shown to significantly improve medication adherence. The purpose of this study is to assess the effect of home-delivered pill packs on medication adherence in a low-income population. This is an open-lab randomized controlled trial taking four or more medication doses daily, randomized either to the intervention group or the control group. Patients in the intervention group received prescriptions pre-packaged in individual packets that were delivered by the pharmacy. Patients in the control group continued to receive medications from pharmacies as they did prior to enrollment. The primary outcome was the percentage of missed pills in the intervention group versus the control group after four months of enrollment.

NCT ID: NCT04105959 Completed - Clinical trials for Inflammatory Response

A Study to Investigate the Effects of RIST4721 on the Inflammatory Response in Healthy Male Subjects Using a Blister Model

Start date: July 25, 2019
Phase: Phase 1
Study type: Interventional

A Randomised, Single-Blind, Placebo-Controlled, Crossover Study to Investigate the Effects of RIST4721, a Novel CXCR2 Inhibitor, on the Inflammatory Response in Healthy Male Subjects Using a Standardized Blister Model

NCT ID: NCT03921515 Not yet recruiting - Clinical trials for Chronic Granulomatous Disease (CGD)

Skin Immunity Sample Collection Involving Blisters and Biopsies

Start date: June 26, 2024
Phase: Early Phase 1
Study type: Interventional

Background: The way the body heals and protects itself from getting sick is called the immune response. Some people with weak immune systems get sick often or get rashes and skin infections. Researchers want to find out how the immune system and skin problems are related so they can help these people. Objective: To learn about how immune response and skin healing are related to each other. Eligibility: People ages 18-65 with hyper IgE syndrome or Job syndrome or people ages 7-65 with chronic granulomatous disease. Healthy volunteers ages 18 65 are also needed. Design: Participants will be screened with: Medical history Physical exam Possible urine tests Participants will have 1 to 3 visits within about a week. Visits will include the following: Participants will have a wells device strapped to the inside of the forearm. It will suction the skin and pull the top layer away to form 8 blisters. The skin over the blisters and the liquid inside will be collected. Participants will have up to 4 skin biopsies. A sharp tool will remove a small plug of skin from the forearm. Participants may have blood and urine tests. The skin on participants skin will be rubbed with a cotton swab. Some participants will have an overnight visit. They will have the blister device placed back on the arm. The wells will be lined up over the blister wounds. The wells will be filled with either saline or the participant s blood serum. The device will be covered and left on the arm for up to 24 hours. Doctors will periodically remove some liquid from the wells.

NCT ID: NCT03856840 Completed - Pemphigoid, Bullous Clinical Trials

Cytokines in Blister Fluids of Bullous Pemphigoid (BP)

BP
Start date: January 29, 2018
Phase:
Study type: Observational [Patient Registry]

This study investigates the differences of Eosinophil Cationic Protein, Tumor Necrosis Factor-alpha and Anti-BP180-NC16A IgG levels of blister fluids in Bullous Pemphigoid patients which appeared before and under treatment subsequently. These molecules will also be measured in blood serum before and under treatment. Changes of titers in serum and differences between blister fluids will be compared to observe whether correlation exists between them. These measures will also be compared between groups of responders and non-responders to the first-line treatment options to analyze correlation with treatment success.

NCT ID: NCT03835806 Recruiting - Blister of Foot Clinical Trials

Blister Eradication Looking at Impact of Experimental Versus Established Regimens

BELIEVER
Start date: April 27, 2019
Phase: N/A
Study type: Interventional

The specific aim of this study is to evaluate whether RockTape has similar efficacy to Elastikon in the treatment of foot blisters in ultramarathon runners. Elastikon with paper tape and spray adhesive is a well-accepted means of blister treatment and has been used by medical staff at over 50 multi-stage ultramarathons around the world. RockTape is another commercially available product that has also been used by runners successfully to treat foot blisters. RockTape's adhesive qualities have a potential advantage over Elastikon, in that it does not require an additional adhesive substituting a level of complexity, weight, and cost for foot care. There have been no studies examining the efficacy of either agent for blister treatment. This randomized controlled trial will compare the traditional method of treating blisters with a multi-step approach of percutaneous drainage, paper tape, spray adhesive and then Elastikon to percutaneous drainage, paper tape and RockTape.

NCT ID: NCT03668834 Recruiting - Vitiligo Clinical Trials

Comparing Recipient Site Preparation Using Dermabrasion, Dermaroller and Liquid Nitrogen Induced Blister in Non Cultured Epidermal Cell Suspension in Stable Vitiligo

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

A COMPARATIVE STUDY BETWEEN RECEPIENT SITE PREPARATION USING DERMABRASION, LIQUID NITROGEN INDUCED BLISTER AND DERMAROLLING SYSTEM IN AUTOLOGOUS NON CULTURED EPIDERMAL CELL SUSPENSION PROCEDURE IN STABLE VITILIGO PATIENTS

NCT ID: NCT03203512 Completed - Clinical trials for Extracellular Vesicles; Generation and Function

Fish Oil-derived N-3 Polyunsaturated Fatty Acids and Extracellular Vesicles

HI-FIVE
Start date: February 16, 2018
Phase: N/A
Study type: Interventional

N-3 polyunsaturated fatty acids (n-3 PUFA), which are abundant in oily fish and fish oils, have been suggested to play a role in reducing the risk of cardiovascular diseases (CVDs) by modifying a wide range of risk factors, such as blood fats, blood clotting, blood vessel function and inflammation. Extracellular vesicles (EVs) are small particles released from various cells when they are activated or damaged. High numbers of EVs in the blood have been associated with a higher risk of CVDs, and it is thought that this is because they carry 'bioactive' components which can affect many processes involved in CVDs. However, very few clinical trials have investigated the relationships between the consumption of n-3 PUFA and circulating EVs. This study aims to investigate the effects of dietary n-3 PUFA on the generation and functional activities of EVs, which would provide new insight into the benefits of n-3 PUFA on cardiovascular health.

NCT ID: NCT03106246 Recruiting - Type2 Diabetes Clinical Trials

Circulating Extracellular Vesicles Released by Human Islets of Langerhans

Start date: December 2016
Phase: N/A
Study type: Observational

Beta-cells release extracellular vesicles (EV) and exosomes under normal and pathophysiologic conditions. These EV contain beta-cell specific autoantigens which may trigger the immune response at the initiation of type 1 diabetes. In this study, beta-cell derived EV will be detected and characterized in human blood samples.

NCT ID: NCT02931045 Completed - Clinical trials for Myocardial Infarction

Antiplatelet Therapy Effect on Extracellular Vesicles in Acute Myocardial Infarction

AFFECT EV
Start date: December 30, 2017
Phase: Phase 4
Study type: Interventional

Platelet activation and aggregation leads to myocardial infarction. Platelet P2Y12 receptors are essential for platelet activation. Antagonists against the P2Y12 receptor, which are established in secondary prevention of myocardial infarction, have unexplained anti-inflammatory effects. A novel P2Y12 receptor antagonist ticagrelor reduced infection-related mortality compared to clopidogrel, previous standard treatment for patients with myocardial infarction. Activated platelets release pro-inflammatory and procoagulant platelet extracellular vesicles. The investigators assume that decrease in infection-related mortality in patients treated with ticagrelor may be explained by greater inhibition of the release of platelet vesicles by ticagrelor, compared to clopidogrel. This study is expected to identify an additional mechanism of action of ticagrelor, which might contribute to the observed clinical benefits in patients treated with ticagrelor.

NCT ID: NCT02810002 Completed - Back Pain Clinical Trials

Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

Start date: August 2014
Phase: Phase 1/Phase 2
Study type: Interventional

One hundred infantry recruits will be randomly assigned to two groups. Injuries will be monitored.