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Diaper Rash clinical trials

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NCT ID: NCT02614248 Active, not recruiting - Dermatitis, Contact Clinical Trials

The Use of Coconut Oil for the Prevention and Treatment of Diaper Dermatitis in the NICU Population

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

The purpose of the study is to examine the safety and effectiveness of the use of coconut oil for the prevention and treatment of diaper dermatitis among NICU babies at Genesis Medical Center, Davenport.

NCT ID: NCT02570698 Completed - Diaper Dermatitis Clinical Trials

BM Collection From NICU Infants for Composition

Start date: October 2015
Phase: N/A
Study type: Observational

The primary objective of this study is to collect feces from premature infants over a five weeks period to characterize its composition. Metabolomics, Proteomics, Genomics and Microbiome analyses and cell-based assays will be performed to identify individual components present in feces, which may contribute to the onset of irritation in the diapered area of premature infants.

NCT ID: NCT02475512 Terminated - Pressure Ulcer Clinical Trials

Comparison of Wash Wipes and Standard Care in the Prevention of Incontinence-associated Dermatitis in Elderly

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

Incontinence is a widespread problem in all health care setting. One of the main complications of incontinence is inflammation of the skin in the genital and anal region, also known as incontinence-associated dermatitis (IAD). IAD is a known risk factor of pressure ulcer development. Prevalence figures of IAD vary between 5.6% and 50%. The primary aim of this study is to compare the effectiveness of a 3-in-1 genital wipe versus standard care (traditional water and soap) for the prevention of IAD. The second aim is to perform a health economic evaluation of the 3-in-1 genital wipe versus standard care, and third to compare the cost of a 2-in-1 total body wash wipe versus standard care for total body wash. Other outcomes are the comfort and tolerance of both the nurses and participants. In this Randomized Controlled Trial, performed in 13 long-term care settings, the participants will undergo a 30 day study period. In the experimental intervention, the participants will be washed with body wash wipes and genital wipes. In the control group, the subjects will receive traditional care. IAD as well as Pressure Ulcer prevalence will be monitored. Subjective and objective time measurements will be performed.

NCT ID: NCT02299206 Terminated - Diaper Rash Clinical Trials

CeraVe Cream Compared to Desitin Paste for Treating Diaper Dermatitis in Infants

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

This is a single-center, 1:1 randomized, double-blind, parallel-group, non-inferiority controlled trial to demonstrate non-inferiority of CeraVe Baby Diaper Rash Cream compared to Desitin Maximum Strength Original Paste when administered to children with diaper dermatitis who are between 3 months to 18 months of age. Parents/caregivers of subjects in both groups will administer the product with each diaper change throughout the course of the study period. Product can be applied liberally as needed. Diapers and skin cleansing interventions will stay constant throughout the treatment period. Subjects will be assessed by the study doctor, parent/caregiver will be asked about any adverse effects. Parent/caregivers will also be asked to complete a daily diary that asks about changes in their baby's diaper dermatitis, a Visual Analogue Scale severity assessment of their baby's diaper dermatitis, and observations related to product use and the baby's comfort level. Parents/caregivers will also be given a questionnaire rating the use of the study products.

NCT ID: NCT01167465 Withdrawn - Diaper Rash Clinical Trials

Determination of Safety and Consumers' Satisfaction of Moussik Versus Desitin Creamy Ointment in Diaper Rash Prophylaxis

Start date: January 2013
Phase: Phase 4
Study type: Interventional

The purpose of this clinical observation is to evaluate the safety and consumers' satisfaction of Moussik vs Desitin Creamy ointment as a diaper rash protection product.

NCT ID: NCT00702507 Completed - Diaper Rash Clinical Trials

Prospective Two-Year Study to Assess Miconazole Nitrate Resistance in Neonates and Infants

Start date: May 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether repeated use of 0.25% miconazole nitrate ointment in newborns and infants with a yeast infection in the diaper area causes the yeast to become resistant to the drug.

NCT ID: NCT00219466 Completed - Diaper Rash Clinical Trials

Clinical Study to Evaluate the Efficacy and Safety of Two Marketed Investigational Products in Children With Diaper Rash

Start date: June 2005
Phase: Phase 4
Study type: Interventional

To evaluate whether Desitin; Zinc Oxide Diaper Rash Ointment (Desitin Original) and Desitin Creamy; Zinc Oxide Diaper Rash Ointment (Desitin Creamy) provide relief of the signs and symptoms associated with diaper rash after 12 and 24 hours of product application.