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Infections clinical trials

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NCT ID: NCT02164409 Recruiting - Clinical trials for Bacterial Infection Due to Helicobacter Pylori (H. Pylori)

Changes Associated With H. Pylori and Gastric Carcinogenesis

IIT H pylori
Start date: July 2012
Phase:
Study type: Observational

This is a research study for patients who currently have or previously had an H. pylori infection or who have gastric or esophageal cancer and who plan to undergo an endoscopy as part of their care. The purpose of this study is to find out how and why H. pylori infections can cause progression to gastric cancer and if it's possible for intervention prior to this progression.

NCT ID: NCT02143401 Active, not recruiting - Cirrhosis Clinical Trials

Navitoclax and Sorafenib Tosylate in Treating Patients With Relapsed or Refractory Solid Tumors

Start date: November 7, 2014
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and the best dose of navitoclax when given together with sorafenib tosylate in treating patients with solid tumors that have returned (relapsed) or do not respond to treatment (refractory). Navitoclax and sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT02143245 Active, not recruiting - Clinical trials for Total Shoulder Arthroplasty

Diagnostic Accuracy of Synovial Biopsy for Implant-Related Shoulder Infections

Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of retrieving tissue samples via an x-ray guided needle that is inserted into the infected tissue in the shoulder. The procedure using the guided needle is called a synovial biopsy versus an open tissue biopsy, which is done at the time of surgery. By doing the synovial biopsy prior to a revision surgery, the investigators hope to avoid more invasive intervention if it is not needed. Some patients may appear to have an infection but once the biopsy is taken and the results are read, there may not be an infection and therefore no need for a revision surgery.

NCT ID: NCT02139423 Completed - Clinical trials for Congenital Cytomegalovirus Infection

Diagnosis of Congenital CMV Infection in Neonates Who Failed Newborn Hearing Screening

CymeAudit
Start date: November 22, 2014
Phase: N/A
Study type: Interventional

Universal hearing screening at birth by use of otoacoustic emission (OAE) is now offered in most maternities in France to detect symptomatic hearing impairment at birth but screening of cCMV infection is not coupled with this screening. In this study, the feasibility of achieving before one month of age the diagnosis of congenital CMV diagnosis and as well as the confirmation of hearing loss in newborns who failed newborn hearing screening will be tested.

NCT ID: NCT02137603 Completed - Clinical trials for Suppurative Appendicitis

Fast Track Appendectomy for Suppurative Appendicitis

Start date: April 2014
Phase: N/A
Study type: Interventional

The literature has reported that fast track surgery can be safely applied to children undergoing appendectomy for acute appendicitis. There is no current evidence regarding the application of same day discharge protocol in children with intra-operative findings of suppurative appendicitis. The current standard of care for patients who present with intra-operative findings of suppurative appendicitis includes post-operative admission and treatment with intravenous antibiotics. Patients are discharged home once they have met the following discharge criteria: temperature less than 38.5 degrees Celsius, pain control with oral pain medication, and tolerating a liquid diet. Given the evidence in the literature that has shown that same day discharge of patients with acute appendicitis is safe and effective, we propose that fast track surgery protocol can be safely applied to patients with intraoperative findings of suppurative appendicitis. We hypothesize that this will result in a decreased postoperative length of stay, without an increase in 30-day complication rate.

NCT ID: NCT02136797 Recruiting - CMV Infection Clinical Trials

Trial of Third Party Donor Derived CMVpp65 Specific T-cells for The Treatment of CMV Infection or Persistent CMV Viremia After Allogeneic Hematopoietic Stem Cell Transplantation

Start date: May 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see how well transfusions of T-cells work in treating CMV. Tcells are a type of white blood cell that helps protect the body from infection. A transfusion is the process by which blood from one person is transferred to the blood of another. In this case, the T-cells are made from the blood of donors who are immune to CMV. The T-cells are then grown and taught to attack the CMV virus in a lab.

NCT ID: NCT02135419 Active, not recruiting - HIV Infection Clinical Trials

Treatment in Preventing Anal Cancer in Patients With HIV and Anal High-Grade Lesions

ANCHOR
Start date: September 24, 2014
Phase: Phase 3
Study type: Interventional

The randomized phase of the trial compared topical or ablative treatment with active monitoring in preventing anal cancer in patients with human immunodeficiency virus (HIV) and high-grade squamous intraepithelial lesions (HSIL). Anal HSIL is tissue in the anal canal that has been damaged by infection with human papillomavirus (HPV) and is at risk for turning into anal cancer. The ANCHOR Data Safety Monitoring Board (DSMB) determined that the primary study endpoint was completed, based on the data and statistical analysis presented to them on 07SEP2021. In the post-randomization phase of this trial, all enrolled participants are offered treatment for HSIL and/or follow-up, at the participant's choice.

NCT ID: NCT02134392 Recruiting - Clinical trials for Clostridium Difficile

Fecal Transplant for Pediatric Patients Who Have Recurrent C-diff Infection

FMT
Start date: December 2013
Phase: Phase 1
Study type: Interventional

C-diff infection often causes belly pain and diarrhea and can be very hard to treat with medicine. One of the possible reasons that C-diff infection is hard to treat is because there is too much "bad" bacteria in the colon. Investigators believe that putting more "good" bacteria into the colon will help fight the "bad" bacteria. We do this by doing a fecal (poop) transplant. Fecal transplant has been done at other hospitals, but not at Nationwide Children's Hospital. Since our Investigators have not done this before, this study will help us learn the best way to do the transplant. Investigators also believe this transplant might help improve symptoms for patients with C-diff.

NCT ID: NCT02134301 Recruiting - Clinical trials for Gram Positive Bacterial Infections

Open-Label, Dose-Finding, Pharmacokinetics, Safety and Tolerability Study of Oritavancin in Pediatric Patients With Suspected or Confirmed Bacterial Infections

Start date: May 2014
Phase: Phase 1
Study type: Interventional

The purpose of this Phase 1 trial is to evaluate the pharmacokinetics, safety and tolerability of oritavancin in patients <18 years old with a confirmed or suspected bacterial infection.

NCT ID: NCT02134184 Completed - Influenza Clinical Trials

The Influence of Chronic CMV Infection on Influenza Vaccine Responses

SLVP025
Start date: October 2012
Phase: Phase 4
Study type: Interventional

In this study we are trying to understand whether previous infection with a particular virus, namely cytomegalovirus (CMV), influences the ability of the immune system to respond to new infections or vaccinations with age.