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Infection clinical trials

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NCT ID: NCT02032056 Terminated - Allergy Clinical Trials

Effect of Probiotics in Reducing Infections and Allergies in Young Children During the Complementary Feeding Period

ProbiComp
Start date: September 2013
Phase: N/A
Study type: Interventional

The aim of the intervention is to examine the effect of the bacterial strain BB-12, provided for 6 mo, on the prevalence of infections and allergic manifestations in small children, and how BB-12 affects the immune system, the gastrointestinal tract and the microbiota. Children are enrolled during 2 winter seasons.

NCT ID: NCT02027532 Terminated - Infection Clinical Trials

Prevention of Infection in Closed Fractures: Cefazolin Versus Vancomycin

Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the incidence rate of infection in surgical patients with closed fractures treated prophylactically with Cefazolin versus Vancomycin in the peri-operative period. The hypothesis of this study is that patients undergoing surgical treatment for closed fractures who are treated prophylactically with Vancomycin will have a lower incidence rate of infection than patients who are treated prophylactically with Cefazolin.

NCT ID: NCT01964885 Terminated - Common Cold Clinical Trials

Benefit and Tolerability of IQP-AS-105 in Reducing Susceptibility to Upper Respiratory Tract Infections

Start date: October 2013
Phase: Phase 3
Study type: Interventional

IQP-AS-105, is a food supplement derived from garlic (Allium sativum). The objective of this study is to evaluate the possibilities of clinical use of IQP-AS-105 as a preventive medicine, based on its ability to enhance the immune system responses

NCT ID: NCT01935986 Terminated - Clinical trials for Upper Respiratory Tract Infection

The Effect of a Probiotic on Protection Against Upper Respiratory Tract Infections in Children

Start date: August 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to study the effect of a probiotic on protection against upper respiratory tract infections (URTI) in children.

NCT ID: NCT01928693 Terminated - Corneal Ulcers Clinical Trials

A Comparison of Three Fluoroquinolone Topical Eyedrops in the Treatment of Infectious Corneal Ulcers.

Eye02
Start date: July 2013
Phase: Phase 2
Study type: Interventional

This Phase II study will evaluate the safety and efficacy of three fluoroquinolone ophthalmic agents to determine the optimal treatment in patients with infectious corneal ulcers.

NCT ID: NCT01924806 Terminated - Lower Leg Wound Clinical Trials

A Pilot Study of the WoundWand™ Debridement Device on Infection Prevention

WoundWand
Start date: March 4, 2014
Phase: N/A
Study type: Interventional

A Pilot Study of the WoundWand™ Debridement Device on Infection Prevention

NCT ID: NCT01861561 Terminated - Infection Clinical Trials

Low-dose VS High-dose IV Cyclophosphamide for Proliferative LN in Children

Low/highIVCY
Start date: May 2013
Phase: Phase 4
Study type: Interventional

Proliferative lupus nephritis (LN)is the predominant cause of morbidity and mortality in juvenile Systemic Lupus Erythematosus (SLE). Induction therapy with high-dose intravenous cyclophosphamide can improve renal outcomes, but considerably associated with infection. Although severe infection is the significant complication related to poorer prognosis for juvenile SLE patients in Asia, cyclophosphamide is still commonly used as the drug of choice for severe lupus nephritis. Euro-Lupus Nephritis Trial demonstrated low-dose intravenous cyclophosphamide regimen followed by azathioprine achieved good clinical results comparable with obtained high-dose regimen. There was lower number of severe infection episodes, but no significant difference. Recent studies applied low dose of cyclophosphamide (500 mg/m2/dose or 500 mg/dose)in young patients and showed good renal response. Low-dose intravenous cyclophosphamide regimen might promote non-inferior renal remission whereas decrease risk of serious infection and improve overall patient outcomes.

NCT ID: NCT01821963 Terminated - Infection Clinical Trials

Telaprevir Plus Standard of Care (SOC) in HCV Associated Hepatocellular Carcinoma (HCC)

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The goal of this clinical research study is to learn if the antiviral combination of telaprevir, pegylated Interferon Alfa 2a (PegIFN alfa-2a) and ribavirin (RBV) can prevent the virus from coming back after the liver transplant. Telaprevir, PegIFN alfa-2a, and RBV are different antiviral drugs that work in combination at different stages of the HCV infection to stop the virus.

NCT ID: NCT01803919 Terminated - Clinical trials for Urinary Tract Infection

Efficacy Study of Antimicrobial Catheters to Avoid Urinary Infections in Spinal Cord Injured Patients

ESCALE
Start date: November 2012
Phase: N/A
Study type: Interventional

The purpose of this trial is to make a comparison between the use of antiseptic silver alloy-coated silicone urinary catheters and the use of conventional silicone urinary catheters in spinal cord injured patients to prevent urinary infections.

NCT ID: NCT01789697 Terminated - Pain Clinical Trials

Text Message Study

Start date: September 2012
Phase: N/A
Study type: Interventional

The objectives of this double-blind, randomized, controlled study are to evaluate the efficacy of maintaining contact with low-back pain patients through text messaging and emailing, to decrease anxiety levels, pain, number of follow-up visits through text messaging and emailing, and to improve reporting of surgical site infection after spine surgery through text messaging and emailing. The outcomes that will be measured are anxiety, pain, follow-up visits and received phone calls, and reporting signs of surgical site infection. Participants will include Dr. Oren Gottfried's patients who underwent spine surgery at Duke Hospital or at Duke Raleigh Hospital. Patients will be approached after determination that the patient is going to undergo spinal surgery. All patients meeting inclusion criteria will be approached to participate irrespective of race or ethnicity. A total of 194 subjects will be recruited.