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Skin Diseases, Infectious clinical trials

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NCT ID: NCT00646958 Completed - Abscess Clinical Trials

Safety and Efficacy Study of Oxazolidinones to Treat Uncomplicated Skin Infections

Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of RX-1741, an oxazolidinone, versus linezolid, another oxazolidinone, in the treatment of uncomplicated skin and skin structure infections

NCT ID: NCT00619710 Completed - Cellulitis Clinical Trials

Complicated Skin and Skin Structure Infections

Start date: February 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the non-inferiority of meropenem (Merrem) and imipenem in hospitalised subjects with complicated skin and skin structure infections.

NCT ID: NCT00560599 Completed - Clinical trials for Methicillin Resistant Staphylococcus Aureus Skin Infections

A Randomized Clinical Trial to Prevent Recurrent CA-MRSA Infection

PRIMO
Start date: April 2007
Phase: Phase 3
Study type: Interventional

This clinical trial tests the hypotheses that 1) body decolonization of patients with recurrent community-associated (CA) MRSA infections and their household members and 2) environmental decolonization of the patients' households will significantly reduce the likelihood of recurrent CA-MRSA infection.

NCT ID: NCT00555061 Completed - Clinical trials for Skin Infections, Bacterial

Pharmacokinetics of Retapamulin in Pediatric Subjects With Uncomplicated Skin Infections.

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

A study to evaluate the pharmacokinetics of Retapamulin Ointment, 1%, in pediatric subjects (2-24 months) with secondarily-infected traumatic lesions, secondarily-infected dermatoses, or impetigo (bullous and non-bullous).

NCT ID: NCT00514527 Completed - Wounds and Injuries Clinical Trials

A Study for Patients With Complicated Skin and Skin Structure Infections

SIMPLIFI
Start date: August 2007
Phase: Phase 2
Study type: Interventional

Two Phase III trials to demonstrate the efficacy and safety of oritavancin in the treatment of complicated skin and skin structure infections (cSSSI) have been completed. The pharmacokinetic profile of oritavancin in humans suggests that oritavancin has the potential to be used safely and effectively when given either as a single dose or as an infrequent dose for cSSSI. Data from animals support this theory. SIMPLIFI has been designed to evaluate the efficacy and safety of either a single dose of oritavancin or an infrequent dose of oritavancin (First dose on Day one with an option for a second dose on Day five) compared to the previously studied dosing regimen of 200mg oritavancin given once daily for 3 to 7 days.

NCT ID: NCT00513799 Completed - Clinical trials for Staphylococcus Aureus

The Natural History of Community-Associated MRSA Infections and Decolonization Strategies

StLStaRS
Start date: March 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the natural history of community-associated Staphylococcus aureus infections in both adult and pediatric patients by monitoring the rate of recurrent infections in those colonized with S. aureus. In addition, this study will evaluate the efficiency of commonly prescribed decolonization measures in patients presenting with S. aureus skin and soft tissue infections.

NCT ID: NCT00492271 Terminated - Clinical trials for Community Acquired Pneumonia

First Time in Man Trial for Friulimicin B

Start date: June 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to study the safety of single doses and multiple doses of Friulimicin B in healthy volunteers. The level of Friulimicin B will be measured in the subjects blood and urine. One part of the study will assess if Friulimicin B in the plasma of subjects has activity against bacteria.

NCT ID: NCT00488761 Completed - Clinical trials for Skin Diseases, Infectious

Study Evaluating the Safety and Efficacy of Tigecycline in Hospitalized Patients With cSSSI

Start date: July 2006
Phase: Phase 4
Study type: Interventional

Tigecycline's activity against resistant organisms, as well as significant coverage of both gram-positive and gram-negative bacteria, may provide a valuable therapeutic alternative in treating patients with complicated skin and/or skin structure infections.

NCT ID: NCT00488345 Completed - Clinical trials for Bacterial Infections

Study Evaluating the Pharmacokinetics (PK), Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age

Start date: December 2007
Phase: Phase 2
Study type: Interventional

To determine the pharmacokinetic profile and to evaluate the safety and tolerability of ascending multiple doses of tigecycline in patients aged 8 to 11 years with selected serious infections; complicated intra-abdominal infections (cIAI), complicated skin and skin structure infections (cSSSI), or community-acquired pneumonia (CAP).

NCT ID: NCT00475930 Completed - Clinical trials for Staphylococcus Aureus

Chlorhexidine Impregnated Cloths to Prevent Skin and Soft Tissue Infections in Marine Officer Candidates

Start date: May 2007
Phase: N/A
Study type: Interventional

Outbreaks of skin and soft tissue infections (SSTI) related to community associated Methicillin-resistant Staphylococcus aureus (MRSA) have become increasingly common in military training units. Risk factors for MRSA related SSTI such as crowding, poor hygiene and shared equipment are often hard to avoid in a military training environment, often designed to simulate battlefield conditions. It has recently been demonstrated that military recruits colonized with MRSA may be at increased risk of developing SSTI. Studies in the hospital environment have shown that decolonizing inpatients known to carry MRSA decreases the rates of MRSA related infections in the treated individuals and also in their inpatient unit as a whole. The investigators propose a randomized, double blind, placebo controlled trial to: 1. Evaluate the effectiveness, feasibility, and safety of chlorhexidine body cloths, self-administered three times weekly, in preventing SSTI among recruits in military training facilities; and 2. Evaluate the effectiveness of chlorhexidine body cloths in decreasing rates of Staphylococcus aureus colonization among military recruits.