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Candidiasis clinical trials

View clinical trials related to Candidiasis.

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NCT ID: NCT01293643 Completed - Clinical trials for Vaginosis, Bacterial

A Study to Compare the Efficacy and Safety of a Combination of Ketoconazole and Clindamycin Compared to Tetracycline/Amphotericin B Combination Cream for the Treatment of Bacterial Vaginosis and Vaginal Candidiasis (P08077)

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

This is a study to compare the safety and efficacy of the use of a intravaginal ovule containing a combination of Ketoconazole and Clindamycin to the use of an intravaginal cream containing a combination Tetracycline and Amphotericin B for the treatment of bacterial vaginosis and/or mixed or isolated vaginal candidiasis.

NCT ID: NCT01273922 Completed - Candidiasis Clinical Trials

Safety and Immunogenicity Study of a Recombinant Protein Vaccine (NDV-3) Against S.Aureus and Candida

Start date: January 2011
Phase: Phase 1
Study type: Interventional

This randomized, double-blind, placebo-controlled study is a first-in-human Phase 1 study using two dose levels of an investigational vaccine directed against S. aureus and Candida. The study is designed to evaluate the safety, tolerability and immunogenicity of the investigational vaccine, NDV-3

NCT ID: NCT01253954 Recruiting - Candidiasis Clinical Trials

A Multicenter Observational Study of Invasive Candida Infections Among ICU Patients in China

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

The incidence of invasive candida infection (ICI) in critically ill patients is increasing day by day. The crude mortality of IFI in ICU could be as high as 25%-75% depending on their age, underlying conditions, and so on. Candida albicans was by far the predominant species in most countries, causing up to two thirds of all cases of invasive candidiasis. However, a shift toward non-albicans Candida species has been observed. Although the studies of ICI cause universal attention recently, there is still no large-scale, multi-center epidemiological research in China focusing on ICI in critically ill patients, therefore we conducted a large-scale multi-center observational study of IFI in critically ill patients named "China Scan" (CHINA Survey of Candidiasis in ICU) to assess the current incidence, mortality, pathogen spectrum, management, and risk factors for ICI in China ICUs.

NCT ID: NCT01237795 Completed - Dental Plaque Clinical Trials

Experimental Denture Pastes

Start date: February 2008
Phase: N/A
Study type: Interventional

This trial aims to evaluate the efficacy of three experimental dentifrices to remove denture biofilm. Complete denture wearers will be instructed to brush their dentures with a specific toothbrush and four compositions: (1) A proprietary denture-specific paste (active comparator); (2) 0.2% chloramine T; (3) 1.0% chloramine T; (4) 0.01% fluorosurfactant. Each treatment will be used for periods of 7 days, and participants will be randomized to use them according to one of four sequences.

NCT ID: NCT01237782 Completed - Dental Plaque Clinical Trials

Efficacy of a Propolis-based Denture Cleanser

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

The purpose of this study is to assess if a propolis solution is able to remove plaque and kill microbes from complete dentures. The investigators will compare the results of the propolis-based denture cleanser with those obtained with an inactive solution.

NCT ID: NCT01230814 Completed - Bacterial Vaginosis Clinical Trials

Topical Metronidazole and Miconazole Co-formulated Vaginal Suppositories for Preventing Vaginal Infections in HIV-seronegative Women

Start date: April 2011
Phase: Phase 2
Study type: Interventional

This research study is about vaginal infections such as bacterial vaginosis, yeast infections, and trichomoniasis. Usually, these infections can be treated with medication, but sometimes they come back after treatment. Researchers want to know if using vaginal suppositories can decrease the risk of vaginal infections. Participants will include 234 women who are sexually active (greater than or equal to 4 episodes of sex with men during the past month), HIV-negative, 18 to 45 years old, with bacterial infection [vaginosis and/or vulvovaginal candidiasis (VVC) and/or Trichomonas vaginalis] detected by laboratory testing at a screening visit. Women will receive vaginal suppositories containing drug or inactive ingredients (placebo). Participation in the study will be about 12 months. Study procedures include: urine and blood tests, physical exams, and questionnaires.

NCT ID: NCT01213823 Terminated - Candidemia Clinical Trials

Risk Of Severe Hepatic Injury In Patients With Invasive Candidiasis Treated With Echinocandins

Start date: September 2008
Phase: Phase 4
Study type: Observational

The purpose of this study is to estimate the relative risk of severe hepatic injury in hospitalized patients with invasive candidiasis and candidemia who received anidulafungin, compared to patients who received caspofungin and/or micafungin.

NCT ID: NCT01207843 Completed - Leukemia Clinical Trials

Optimized Radiological Diagnosis of Hepatic Candidiasis During the Treatment of Acute Leukemias

Start date: October 2009
Phase: Phase 4
Study type: Observational

Hepatic candidiasis is a frequent complication in patients receiving intensive chemotherapy for acute leukemia. Hepatic lesions may be detected by computerized tomographic (CT) scans, but there is no standardized CT protocol for the diagnosis and follow-up of hepatic candidiasis. The investigators compared the size of the fungal lesions in the chest and abdomen CT. The current analysis aimed to increase the value of CT for the diagnosis and the follow-up of hepatic candidiasis in daily routine.

NCT ID: NCT01202253 Completed - Candidiasis Clinical Trials

Early Clinical Experience With Anidulafungin In Patients With Liver Disease In The United Kingdom

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to describe the real world effectiveness of anidulafungin in clinical practice in a large Liver Unit in the United Kingdom.

NCT ID: NCT01176058 Terminated - Candidemia Clinical Trials

A Study Of The Efficacy And Safety Of Anidulafungin Vs. Fluconazole In The Treatment Of Patients With Candidemia And/Or Other Forms Of Invasive Candidiasis

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

In the treatment of patients with candidemia and/or other forms of invasive candidiasis , Anidulafungin is at least as effective and safe as Fluconazole.