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Infection clinical trials

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NCT ID: NCT03888898 Completed - Infection Clinical Trials

Just-in-time Elastomeric Training and Fit Testing (JET FIT)

Start date: April 2, 2019
Phase: N/A
Study type: Interventional

This is a clinical trial to evaluate feasibility of a just in time elastomeric half mask respirator (EHMR) fit test and competency training for healthcare personnel (HCP) during a simulated public health emergency.

NCT ID: NCT03883399 Completed - Clinical trials for Surgical Site Infection

Survey on Practice and Comparison With Best Evidence in Surgical Site Infection Prevention in Colorectal Surgery

PREVISQCOR
Start date: November 1, 2018
Phase:
Study type: Observational

Web-based survey to colorectal surgeons assessing knowledge, beliefs and practices regarding the use of preventative measures for SSI.

NCT ID: NCT03883022 Recruiting - Spinal Stenosis Clinical Trials

Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery

Start date: September 3, 2018
Phase: N/A
Study type: Interventional

Deep surgical site infection (DSSI) is one of the most challenging complications for spinal surgeons and can lead to a poor clinical outcome. This ambispective study was designed to examine the effect of vancomycin powder mixed with autogenous bone graft and bone substitute on preventing deep surgical site infection (DSSI) in degenerative lumbar fusion surgeries as well as any interference with bony fusion.

NCT ID: NCT03880682 Completed - Clinical trials for Hepatitis C, Chronic

Direct Acting Antivirals for HCV Infection in Kidney Transplant Recipients

Start date: November 1, 2018
Phase:
Study type: Observational

Chronic hepatitis C virus (HCV) infection, an important cause of morbidity and mortality worldwide, is a significant problem in kidney transplant recipients (KTRs) given its high prevalence in patients undergoing hemodialysis. Interferon based regimens were cornerstone of treatment of HCV infection in the past; however, due to their low efficacy and high rates of adverse effects, they have been abandoned in the new era of direct acting antivirals (DAAs). Several studies demonstrated the efficacy and safety of DAAs, yet data regarding clinical practice of these agents in KTRs is still needed. Therefore, we conducted a study using our registry data to evaluate the efficacy and safety of DAAs in KTRs.

NCT ID: NCT03877536 Withdrawn - HIV Infections Clinical Trials

Antiretroviral Therapy for Acute HIV Infection

Start date: March 17, 2019
Phase: N/A
Study type: Interventional

This study will evaluate the virologic effect, safety and tolerability of Genvoya® in adults during early acute HIV infection.

NCT ID: NCT03875963 Terminated - Infection Clinical Trials

Antibiotic Loaded Calcium Sulfate RCT

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

This is a multi-centered, prospective, randomized controlled trial comparing current standard of care for defect management to placement of antibiotic loaded Stimulan as a bone void filler in patients undergoing treatment of infected tibial defects or infected tibial nonunions.

NCT ID: NCT03873350 Completed - Clinical trials for Microbial Colonization

The Effect of the Fermented Tea Beverage Kombucha on the Oral and Gut Microflora

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The purpose of the project is to investigate if consumption of the fermented tea beverage kombucha has an effect on the gut and/or oral microbiota, and further if it depends on the content of living bacteria or is inherent even to sterilized kombucha. This will be studied by a clinical trial in which healthy individuals will be given living kombucha, sterilized kombucha or water. The participants will consume one bottle (33 cl) of their designated drink per day for 21 days. Fecal and saliva samples will be collected before, directly and ten days after the intervention. These will then be examined to see if there is a change in the micro flora due to the kombucha.

NCT ID: NCT03870061 Completed - Tuberculosis Clinical Trials

Evaluation of an Infant Immunization Encouragement Program in Nigeria

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Previous studies have shown that a small incentive can have a large impact on health behaviors like vaccinating children. New Incentives, an international non-governmental organization (NGO), aims to boost demand for immunization by offering cash incentives to caregivers who have their child vaccinated at a program clinic. In collaboration with New Incentives, IDinsight is conducting a study to see whether this approach will increase immunization in North West Nigeria. This study aims to investigate whether giving cash to caregivers in North West Nigeria who bring their infants to receive vaccination against common infections (tuberculosis, diphtheria, tetanus, pertussis, hepatitis B virus (HBV) infection, Haemophilus influenzae Type B (Hib), pneumococcal bacteria, measles, rotavirus, polio, yellow fever) increases the proportion of children who are immunized. The study's main hypothesis is that New Incentives' program will increase the percentage of children immunized with BCG, any PENTA, or Measles 1 by an average increase of at least 7-percentage points across all program clinics that share a similar profile to the clinics New Incentives will operate in at scale. The study is taking place in Jigawa, Katsina, and Zamfara States between August 2017 and January 2020.

NCT ID: NCT03869099 Completed - Pneumonia Clinical Trials

Pneumonia Case Management Practices in Pakistan

Start date: May 1, 2018
Phase:
Study type: Observational

Pneumonia in Pakistan continues to be the leading killer of children under five. Although various national and provincial programs have tried to tackle this but they have not been able to achieve the desired outcomes. Additionally, there has been limited in depth evaluation of the practices of pneumonia management at various levels of the community. The investigators, therefore, aim to establish an understanding of pneumonia case management at three levels of healthcare - community, first level care facility and practitioner level. This will be conducted through observations of pneumonia case managements practices of healthcare providers at these three levels across the country by simulated patients. Observation checklists will be developed incorporating settings and behaviors. Observation sites will be randomly selected with 32 observations made in each province. The results of this study will yield the ground reality of pneumonia case management in Pakistan. Based on the results of this study, strategies can be devised to improve case management within the community with models of regular monitoring and supervision.

NCT ID: NCT03868969 Not yet recruiting - Clinical trials for Urinary Tract Infections

Clinical Efficacy of Fosfomycin Trometamol Per os in the Treatment of Documented Male Urinary Tract Infections With ESBL-producing Enterobacteriaceae With ESBL Producing Enterobacteriaceae and Resistance Associated With Fluoroquinolones and Cotrimoxazole (FOSF'HOM)

FOSF'HOM
Start date: April 2019
Phase: Phase 2
Study type: Interventional

The aim of the study was to evaluate the clinical and microbiological efficacy of fosfomycin trometamol (FT) per os in the treatment of documented male urinary tract infections with ESBL-producing enterobacteriaceae