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Communicable Diseases clinical trials

View clinical trials related to Communicable Diseases.

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NCT ID: NCT01094431 Completed - Fever Clinical Trials

Etiology of Uncomplicated Fever in Children <5 in Rural Zanzibar

RDTNEG
Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to study the most common etiologies of uncomplicated fever diseases among children under five years of age in rural Zanzibar.

NCT ID: NCT01092351 Completed - Clinical trials for Urinary Tract Infection

Efficacy and Safety of Nitrofurantoin in the Treatment of Uncomplicated Urinary Tract Infections in Adults

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

The study aims to investigate bacteriological efficacy of a nitrofurantoin formulation given twice daily for seven days in the treatment of adult patients with microbiologically confirmed uncomplicated urinary tract infection. Additional study objectives are to evaluate clinical efficacy as well as safety and tolerability of the nitrofurantoin formulation.

NCT ID: NCT01090102 Completed - HIV Infections Clinical Trials

Mesalamine to Reduce T Cell Activation in HIV Infection

Start date: June 2010
Phase: Phase 4
Study type: Interventional

The objective of this study is to determine whether 12 weeks of mesalamine therapy added to a standard HIV treatment decreases systemic immune activation and inflammation in HIV-infected patients, possibly resulting in better recovery of the immune system. The study hypothesis is that decreasing inflammation directly in the gut may decrease both of these potential causes of chronic inflammation, potentially resulting in an immunologic benefit.

NCT ID: NCT01089712 Completed - Cardiac Surgery Clinical Trials

Management Practices and the Risk of Infection Following Cardiac Surgery

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of the study is to determine the best ways to prevent infections after heart surgery. Participation in the study will last at most 3 months after heart surgery. The study will only collect information about the care patients receive during the planned surgery. No new testing or procedures will be done. Patients will receive only the tests or procedures the doctor already has planned. This kind of study is an observational study, because all that is planned to do is observe the care patients receive and how well they do during treatment. The information collected should help to improve the quality of surgical care in the future.

NCT ID: NCT01089465 Completed - Sting Clinical Trials

Cimex Lectularius or Bed Bugs : Vector of Infectious Agents and Pathogenic Role

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

During the last years, the investigators were the witness to the increase of a old emerging pest due to bed bugs (Cimex lectularius) in the world. Insecticides resistances apparitions and internationals transports increases seem to be the reasons of the pest. Cimex lectularius as vector of parasites, bacteria or virus was often suggested although not much observation are recently investigated in France. This study intends to examine the vectorial ability and the direct pathogenicity of Cimex lectularius.

NCT ID: NCT01088295 Completed - HIV Infection Clinical Trials

HIV and Fat Accumulation

MATH
Start date: May 2010
Phase: Phase 2
Study type: Interventional

This is a research study to see whether fat accumulation either under the skin or in the body's organs, for example, the liver, improves in men and women who take a drug called telmisartan. The investigators will be looking at how the amount of fat in the body changes when HIV-positive persons on effective anti-HIV therapy take telmisartan. The investigators will be using a CT scan to make this comparison. Telmisartan is not an HIV medication. It is a medication used to treat blood pressure, but has been shown to decrease fat in the organs in people both with and without high blood pressure. The study involves 8 visits over a period of about 24 weeks.

NCT ID: NCT01085799 Completed - Infections Clinical Trials

Education Intervention to Reduce Helminth Infections and Absenteeism in Grade 5 School-children

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

To efficiently control soil-transmitted helminths (Ascaris, Trichuris, and hookworm), WHO, PAHO, and others recommend the inclusion of an education strategy in school-based deworming programs. However, the effectiveness of such a strategy on the rate of STH re-infection and on education indicators, such as absenteeism, remains to be fully understood. The proposed research aims to evaluate the effectiveness of a post-deworming education intervention targeted to Grade 5 school children enrolled in Belén's schools using a cluster-randomized trial design. Results will be used to inform school-based deworming programs in Peru and other similar endemic areas in Latin America and, indeed, around the world.

NCT ID: NCT01085786 Completed - Clinical trials for Helicobacter Pylori Infection

Sequential and Hybrid Therapies for H Pylori Infection

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Primary: To evaluate efficacy of 14 day 2-phase sequential therapy given in two forms. One in which the first component consists of a proton pump inhibitor and amoxicillin given for 7 days followed by the PPI, clarithromycin and metronidazole for 7 days. The alternate will be similar with the exception that the amoxicillin will be continued throughout the 14 days. The secondary endpoint is to evaluate the effectiveness of therapy in relation to antibiotic resistance.

NCT ID: NCT01085721 Not yet recruiting - Clinical trials for Viral Infections of the Upper Respiratory Tract

Comparison Between Dexchlorpheniramine and Dexchlorpheniramine/Pseudoephedrine/Guaifenesin in Respiratory Infections

Start date: n/a
Phase: Phase 3
Study type: Interventional

Patients with allergic rhinitis frequently present exacerbation of the atopic symptoms during viral infections of the upper respiratory tract. Also, allergic rhinitis makes the mucosa more reactive to infectious agents and potentiates mucus production. The combination of dexchlorpheniramine, pseudoephedrine and guaifenesin elicits antihistaminic, decongestant and expectorant effects. The study hypothesizes is that this product is superior to dexchlorpheniramine alone in the relief of allergic symptoms and in promoting mucus elimination in atopic patients with viral infections of the upper respiratory tract.

NCT ID: NCT01085669 Recruiting - Infection Clinical Trials

Infection Rate of Vertical Expandable Prosthetic Titanium Rib Implants (VEPTR)

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

The study is conducted to analyse the infection rate in children treated with VEPTR-Implants for severe spine or thoracic deformities.