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Skin Diseases clinical trials

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NCT ID: NCT01405144 Unknown status - Actinic Keratosis Clinical Trials

5fluorouracil for Advanced Photoaging

Start date: August 2010
Phase: Phase 3
Study type: Interventional

It is well known the efficacy of 5% 5-fluoruracil for multiple and superficial actinic keratosis (AKs)treatment. Recently its additional benefit for advanced and severe photoaging while treating Aks was reported. The aim of this study is to compare the efficacy and safety of the two modalities of 5% 5-FU use for forearms photoaging.

NCT ID: NCT01369251 Recruiting - Infection Clinical Trials

Simple Hygiene Versus Alcohol Based Usual Care for Umbilical Cord

Start date: May 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determinate whether in newborns just cleaning the umbilical stump when changing diapers (with water and soap if necessary)is effective in preventing local cord infections and not delaying cord separation as just as cord care alcohol, usually applied in our hospital and suggested to parents at dismission.

NCT ID: NCT01330706 Completed - Skin Diseases Clinical Trials

Efficacy of Intraoperative Surgical Scrubbing in Reducing Bacterial Load After Nail Removal Surgery

ribebeva
Start date: February 2010
Phase: Phase 4
Study type: Interventional

The investigators conducted a controlled, prospective randomized study to examine the antiseptic efficacy of intraoperative irrigation methods during nail avulsion surgery.

NCT ID: NCT01305187 Completed - Skin Diseases Clinical Trials

Non-inferiority of Belotero® Basic Versus Juvéderm® Ultra 3

Start date: February 2011
Phase: Phase 4
Study type: Interventional

This study will investigate the non-inferiority of Belotero® Basic versus Juvéderm® Ultra 3 in the treatment of nasolabial folds

NCT ID: NCT01223222 Completed - Atopic Dermatitis Clinical Trials

A Study to Evaluate Safety, Tolerability and Efficacy of Lytixarâ„¢ (LTX-109) on Uncomplicated, Gram-positive, Skin Infection

Start date: September 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of Lytixarâ„¢ applied topically to uncomplicated skin infections. Three dose levels of Lytixarâ„¢ (1%, 2% and 5%) versus placebo will be tested.

NCT ID: NCT01187732 Completed - Skin Disease Clinical Trials

Washing Without Water: Cost-effectiveness of a Rapidly Spreading Nursing Intervention in Bedridden Patients'

WWW
Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the traditional bed bath with 'washing without water' on - 1) effects on skin integrity - 2) patient and nurse satisfaction and 3) costs. In a cluster randomized trial we will randomize 50 nursing home wards (576 patients) to 'washing without water' or traditional bed baths. Bathing regimens are continued for six weeks. Whereas effects on skin damage are not likely to be specific for setting, these results can be generalized to other patient groups.

NCT ID: NCT01119313 Completed - Atopic Eczema Clinical Trials

Study to Investigate Skin Conditions and Patient Assessment of LAS 41002 in the Treatment of Atopic Eczema

Start date: February 2010
Phase: Phase 2
Study type: Interventional

The aim of the study is an intra-individual comparison of skin conditions in addition to a patient based assessment of product appearance in the topical treatment of atopic eczema.

NCT ID: NCT01082523 Completed - Acne Clinical Trials

"A Randomized, Controlled, Evaluator-blinded Pilot Study to Evaluate the Effect of Automated Text Message Reminders on Patient Compliance With Topical Medications and Its Efficacy on Skin Disease Control in Adolescents and Adults With Mild to Moderate Acne"

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

The purpose of this study is to determine whether an automated electronic reminder system using text messages sent to patient's cell phones will help patients with acne be more compliant with their topical medications and lead to an improvement of their acne. Hypothesis: Automatically delivered electronic reminders in the form of text messages will increase acne patient adherence to topical medications and consequently result in better treatment outcome and higher patient satisfaction

NCT ID: NCT01078987 Terminated - Clinical trials for Nephrogenic Systemic Fibrosis

Plasmapheresis for Nephrogenic Fibrosing Dermopathy (NFD)/Nephrogenic Systemic Fibrosis (NSF)

NFD
Start date: February 2002
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the pathophysiology of nephrogenic fibrosing dermopathy (NFD)/nephrogenic systemic fibrosis (NSF).

NCT ID: NCT01044043 Completed - Clinical trials for Dermatologic Disease of Inpatients in Internal Medicine

Prevalence and Subjective Impairment of Quality of Life (QoL) Due to Dermatologic Diseases in Internal Medicine Patients

Start date: November 2009
Phase: N/A
Study type: Observational

This is a 3 months single centre clinical patient-oriented study to evaluate the prevalence and impairment in QOL of dermatologic diseases in patients hospitalised in internal medicine. Up to 200 patients hospitalised at the division of internal medicine for any reason are going to be offered participation by a patient information form given to patients at the time of admission, as well as oral information about the study. Written informed consent will be obtained by the investigators after patients have had adequate time to consider their participation in the study. Participating patients will be examined clinically for dermatologic pathologies at a single visit. In the case of signs of dermatologic disease, investigators are going to recommend further diagnostic procedures to the physician in charge and/or the referring physician, depending on the urgency of the suspected diagnosis. This procedure is meant to avoid giving referring physicians the impression that active patient acquisition for the department of Dermatology is an aim of this study. Diagnostic procedures that are performed upon suspicion of a specific dermatologic disease at the Division of Internal Medicine are going to be performed during the hospitalisation period. All other diagnostic or operative procedures are going to be advised to the referring physician. Study participants are going to be interviewed by the investigators about impairment in QOL of their illnesses. Two separate questionnaires are going to be filled in by each participant. For measurement of general QOL, the widely used SF-12 questionnaire (8 questions) is going to be used. To measure specific impairment in QOL by dermatologic disease, participants are going to be asked to fill in the DLQI (Dermatology life quality index, 10 questions). Photographic documentation of specific identified lesions will be made and pictures stored exclusively in the secured electronic patient file (KISIM). Medication and all identified diseases will be noted. All diagnostically useful information is going to be recorded in the patient file and transmitted to the referring physician in the discharge letter.