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NCT ID: NCT03807453 Completed - Clinical trials for Microbial Colonization

Comparison of Scalp Microbiota of the Psoriasis and Seborrheic Dermatitis Patients

Start date: April 25, 2019
Phase:
Study type: Observational

A sterile swap specimen taken from the scalp of the patients with psoriasis vulgaris or seborrheic dermatitis and the volunteer control group will be examined in our study. The examples of the microbiota of the patients will be taken both the lesional scalp and the lesion-free part of the scalp. Then, the microbiota differences between the lesioned scalp and the lesion-free scalp of both groups, and the microbiome differences between the two groups and the control group will be evaluated.

NCT ID: NCT03798600 Completed - Critical Illness Clinical Trials

Pharmacokinetics/Pharmacodynamics (PK/PD) of Caspofungin in Intensive Care Unit (ICU) Patients. An Open Observational Study for Antifungal Treatment's Optimization

Start date: January 1, 2016
Phase:
Study type: Observational

PK of Caspofungin in ICU septic patients might be changed as compared to healthy volunteers due to sepsis-related pathophysiology. Sub-optimal plasma and tissue concentrations might be achieved in these patients when drugs are administered at the same dosage/regimen suggested for healthy volunteers.

NCT ID: NCT03796546 Completed - Infection Clinical Trials

Pediatric Infectious Disease Precision Medicine Using Sequencing Evaluation of CSF

PIPSEC
Start date: January 22, 2019
Phase:
Study type: Observational

Prospective, multi-site, study to evaluate the diagnosis rate of DNA and RNA sequencing of cerebrospinal fluid for identification of pathogens directly in patients who have already had a spinal tap to evaluate for infection and were found to have a pleocytosis. Diagnostic rate and clinical utility of concurrent standard testing will be compared to diagnostic rate and clinical utility of DNA and RNA sequencing.

NCT ID: NCT03794648 Completed - HIV-infection/Aids Clinical Trials

The Effectiveness of a Mobile Interactive Supervised Therapy (MIST) Intervention for Improving Adherence to HIV Medication

Start date: February 13, 2018
Phase: N/A
Study type: Interventional

A total of 40 HIV infected patients will be randomly assigned into intervention or control group. Participants in the intervention group will use an smart phone application for two months. Participants will receive reminder notifications and use the app to take and send videos of themselves taking the pill(s), uploaded videos will be centrally reviewed by a study nurse . Control group participants will receive standard care. Antiretroviral Therapy adherence will be measured by self-report, pill count, and smart bottle as well as the App. Participants' perceptions of app using experience will be recorded via face to face interview.

NCT ID: NCT03790254 Completed - Clinical trials for Antibiotic Prophylaxis

D Mannose for Prevention and Treatment of RUTIs

mannoseRUTIs
Start date: January 1, 2010
Phase:
Study type: Observational

The aim of this review is to address clinical reliability, efficacy and safety of long-term treatment with oral D Mannose for the prevention of recurrent urinary tract infections (RUTIs) in females.

NCT ID: NCT03780439 Completed - Gastric Cancer Clinical Trials

Procalcitonin to Predict Infection After Gastrectomy for Gastric Cancer

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

To investigate the diagnostic accuracy of procalcitonin as an early predictor of infection after radical gastrectomy for gastric cancer.

NCT ID: NCT03772769 Completed - Clinical trials for Odontogenic Deep Space Neck Infection

Diagnostic Modalities for Severe Odontogenic Infections Using Rapid, Target Enriched Multiplex PCR (TEM- PCR) by Diatherix

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the sensitivity and specificity of the Target Enriched Multiplex (TEM) polymerase chain reaction (PCR) platform for the rapid molecular diagnosis and treatment of odontogenic deep space neck infections.

NCT ID: NCT03770533 Completed - Clinical trials for Patients Presenting With Suspicion of Infection to the ED

Identifying Patients With Suspicion of Infection in the ED Who Have Low Disease Severity Using MR-proADM - Pilot Study

IDEAL
Start date: December 14, 2018
Phase: N/A
Study type: Interventional

Emergency departments (ED) are becoming increasingly over-crowded, with patients facing prolonged waiting times. Therefore, a safe and rapid assessment that identifies patients with low severity that could be treated as outpatients is essential for improving the workflow within the ED. The rationale of this IDEAL study is to provide guidance to safely decrease the number of hospital admissions through identification of low risk patients with the biomarker MR-proADM. This will be tested in a pilot study first.

NCT ID: NCT03768635 Completed - Clinical trials for Bone and Joint Infection

Necrotizing External Otitis : Study in a Regional Bone and Joint Infection Reference Center

Start date: January 1, 2006
Phase:
Study type: Observational

The malignant external otitis is a rare disease which arises more frequently at the elderly and the diabetics patients. To our knowledge, there are few data and it is not wellc known byclinicians. Nevertheless it exposes to neurological complications potentially serious and crippling.

NCT ID: NCT03759652 Completed - Neurosurgery Clinical Trials

Surgical and Non-surgical Infections of Neurosurgical Patient: Before-after Cohort Study

Start date: January 2003
Phase:
Study type: Observational

Continuous surveillance in 2003-2017 allowed to detect HAIs in patients staying in a 42-bed neurosurgery unit with 6 intensive neurosurgical supervision beds. 10,332 surgical patients were qualified for the study. The study was carried out in the framework of a national surveillance of HAI programme following methodology recommended by Healthcare-Associated Infections Surveillance Network (HAI-Net), European Centre for Disease Prevention and Control. Intervention in this before-after study (2003-2017) comprised standardised surveillance of HAI with regular analysis and feedback.