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Communicable Diseases clinical trials

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NCT ID: NCT02805803 Recruiting - Clinical trials for Prosthetic Joint Infection

Quality of Life Assessment in Patients Undergoing Prolonged Suppressive Antibiotherapy for Prosthetic Joint Infection.

PSA-QOL
Start date: November 9, 2016
Phase: N/A
Study type: Interventional

Prosthetic joint infection (PJI) management is complex and requires prosthesis replacement when symptoms duration is greater than 30 days or debridement with modular set replacement when symptoms duration is lesser than one month. Nevertheless, the prolonged suppressive antibiotherapy (PSA) is the single treatment we can provide to high risk surgical patients and those who refuse reoperation. There is limited data available on PSA modality, its tolerance and efficacy, this lack of data motivated us to concept a prospective study of long term patient follow up with PJI treated with prolonged suppressive antibiotherapy.

NCT ID: NCT02801253 Recruiting - Clinical trials for Prosthetic Joint Infection

Cohort of Prosthetic Joint Infections

COPINS
Start date: September 11, 2015
Phase:
Study type: Observational

Management of prosthetic joint infections (PJI) is a challenging task. These infections include different clinical and microbiological settings calling upon various treatment strategies according to infection type (acute or chronic), bone quality, the involved micro-organism and the patient's general condition and willing. Treatment of PJI combines surgery and prolonged antibiotic therapy. In some patients with a high operative risk prolonged suppressive antibiotic therapy can be used. Lack of large prospective studies motivated the conception of this cohort with a long term follow up, regardless to PJI management procedures.

NCT ID: NCT02779439 Recruiting - CMV Infection Clinical Trials

Partially HLA-matched Third Party Antigen Specific T-cells for Infection Post-stem Cell or Solid Organ Transplantation

R3ACT
Start date: January 2013
Phase: Phase 1
Study type: Interventional

To assess the safety and biological efficacy of therapeutically administered most closely HLA-matched third party donor-derived specific cytotoxic T lymphocytes (CTLs) targeting cytomegalovirus (CMV) or Adenovirus (Adv) or Epstein Barr virus (EBV) or fungi including Aspergillus and Candida species for the treatment of viral infection following allogeneic blood or marrow stem cell or solid organ transplantation.

NCT ID: NCT02777866 Recruiting - Postoperative Pain Clinical Trials

LAW Trial -The Impact of Local Anesthetics Infiltration in Surgical Wound of Gastrointestinal Procedures

LAW
Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the infiltration of 0.5% Bupivacaine in the surgical wound is effective to diminish the pain and the risk of surgical site infections in patients who go to a open gastrointestinal procedure.

NCT ID: NCT02760745 Recruiting - Clinical trials for Severe Bacterial Infection

Fever and Shivering: Frequency and Role in Predicting Serious Bacterial Infection

Start date: January 2016
Phase: N/A
Study type: Observational

Febrile shivering in the pediatric population is assumed to be related to a Severe Bacterial Infection (SBI). Research supporting this assumption is scant. The purpose of this study is to describe the frequency of febrile shivering in the pediatric population arriving at the emergency department and to define its role in predicting a SBI.

NCT ID: NCT02687906 Recruiting - Clinical trials for Bacterial Infections

Dose-finding, Pharmacokinetics, and Safety of VABOMERE in Pediatric Subjects With Bacterial Infections

TANGOKIDS
Start date: July 2016
Phase: Phase 1
Study type: Interventional

A single dose infusion of Vabomere (meropenem-vaborbactam) is being tested for dose-finding, pharmacokinetics, safety, and tolerability in pediatric subjects from birth to less than 18 years of age with serious bacterial infections

NCT ID: NCT02671318 Recruiting - Clinical trials for Cytomegalovirus Infections

Conversion to Sirolimus: Effects in Cytomegalovirus Infection Recurrence

StopCMV
Start date: September 2015
Phase: Phase 4
Study type: Interventional

Cytomegalovirus is the most important opportunistic infection after kidney transplant, with increased in mortality, morbidity and higher costs of transplantation. Despite the favorable efficacy (lower acute rejection) results of the most worldwide used regime, tacrolimus, mycophenolate and prednisone, or the investigators local common regimen, tacrolimus, azathioprine and prednisone, this combinations are associated with higher incidence of cytomegalovirus infection, disease and recurrence. Namely, sirolimus use is associated with decreased risk of cytomegalovirus infection/disease, and there is not a prospective cohort to evaluate the conversion to sirolimus efficacy to decrease the cytomegalovirus infection recurrence. Given this, the investigators propose a study of their own initiative that attends local needs: evaluate the conversion to sirolimus efficacy in decrease the cytomegalovirus recurrence after kidney transplant.

NCT ID: NCT02664168 Recruiting - Clinical trials for Surgical Wound Infection

A Comparative Study to Assess the Prevention of Surgical Site Infection (SSI's) in Revision Total Joint Arthroplasty Patients Treated With Single-Use Negative Pressure Wound Therapy (PICO™) or Standard Care Dressings (AQUACEL® Ag SURGICAL Dressing)

Start date: January 2016
Phase: N/A
Study type: Interventional

The aim of this study is to assess the prevention of incision healing complications in patients undergoing revision TKA and THA treated with either Single-Use NPWT (PICO) compared to standard of care dressings (AQUACEL Ag Surgical Dressing). All patients undergoing a revision TKA and THA who consent to taking part in the study, and meet the eligibility criteria will be included onto the study. Patients will be followed up for a period of up to 3 months to determine if there are any latent incision healing complications

NCT ID: NCT02658903 Recruiting - Urinary Infections Clinical Trials

Prevention of Catheter Associated Lower Urinary Infections Using the Oxys Indwelling Catheter

Start date: January 2016
Phase: Phase 1
Study type: Interventional

The safety and efficacy of a urinary catheter designed to prevent catheter associated urinary infections is studied.

NCT ID: NCT02650518 Recruiting - Clinical trials for Catheter-Related Infections

Controlling Antimicrobial Use Through Reducing Unnecessary Treatment of Catheter Associated Urinary Tract Infections

CARCUTI
Start date: December 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Hypothesis: A short course (3-5 days) of antibiotic therapy (experimental arm) is as safe and effective as a long course of antibiotic therapy for the treatment of catheter-associated urinary tract infections.