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NCT ID: NCT02478229 Terminated - Clinical trials for Hepatitis C Viral Infection

Early Treatment With Sofosbuvir (SOF) and Ledipasvir (LDV) to Prevent HCV Recurrence After Liver Transplantation (OLT)

Start date: June 2015
Phase: Phase 3
Study type: Interventional

The study is a single centre, single arm, open-label, proof of concept study enrolling 20 adult primary liver transplant recipients with genotype 1 HCV infection. Subjects will receive Sofosbuvir (SOF) and Ledipasvir (LDV) starting at time of liver transplantation (OLT) and continues for 12 weeks. Subjects will be receive 24 week post-treatment follow up.

NCT ID: NCT02477800 Terminated - Alzheimer's Disease Clinical Trials

221AD301 Phase 3 Study of Aducanumab (BIIB037) in Early Alzheimer's Disease

ENGAGE
Start date: August 13, 2015
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to evaluate the efficacy of monthly doses of aducanumab in slowing cognitive and functional impairment as measured by changes in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) score as compared with placebo in participants with early AD. Secondary objectives are to assess the effect of monthly doses of aducanumab as compared with placebo on clinical progression as measured by Mini-Mental State Examination (MMSE), AD Assessment Scale-Cognitive Subscale (13 items) [ADAS-Cog 13], and AD Cooperative Study-Activities of Daily Living Inventory (Mild Cognitive Impairment version) [ADCS-ADL-MCI].

NCT ID: NCT02471703 Terminated - Joint Diseases Clinical Trials

Clinical Outcome Following Total Hip Arthroplasty With the SMF Stem

SMF-S&E
Start date: February 27, 2008
Phase:
Study type: Observational

This is a prospective, consecutive series, multicenter clinical study of clinical outcomes following total hip arthroplasty with the SMF stem.

NCT ID: NCT02470312 Terminated - Heart Failure Clinical Trials

MediGuide Registry

Start date: August 18, 2015
Phase:
Study type: Observational [Patient Registry]

The goal of this registry/observational study is to collect data on the clinical utility of MediGuideā„¢ system in cardiac resynchronization therapy (CRT) implantation and electrophysiology (EP) procedures.

NCT ID: NCT02465203 Terminated - Clinical trials for Hepatitis C, Chronic

3-year Follow-up Study to Assess the Viral Activity in Hepatitis C Patients Who Failed Feeder DEB025/Alisporivir Study

Start date: September 6, 2012
Phase: Phase 3
Study type: Interventional

Follow-up for viral activity, changes in liver function and safety in patients with no SVR24 in feeder studies

NCT ID: NCT02463669 Terminated - Splenomegaly Clinical Trials

The Use of Point-of-Care Ultrasound in the Diagnosis of Acute Infectious Mononucleosis in the Emergency Department

Start date: April 2016
Phase:
Study type: Observational

The purpose of this study is to determine if splenomegaly on point-of-care ultrasound (POCUS) is an accurate and user-friendly surrogate to the heterophile antibody test and Epstein-Barr Virus (EBV) serologies to diagnose acute mononucleosis infection in patients presenting with sore throat to the Emergency Department (ED).

NCT ID: NCT02463175 Terminated - Acute Kidney Injury Clinical Trials

Effects of Goal-directed Fluid Therapy on Post-operative Outcomes in Children Undergoing Scoliosis Repair

CardioQ-RP
Start date: June 2015
Phase: N/A
Study type: Interventional

Surgery for scoliosis correction, the abnormal curvature of the spine, is a major procedure often undertaken in adolescents. In adult anesthesia, there is a large volume of literature debating how to optimize fluids administered during surgery, as both too much fluid and too little fluid are associated with worse outcomes. The investigators will compare fluid administration based on the measured amount of blood pumped by the heart during each heart beat (goal-directed therapy), against standard anesthetic management. The main outcomes are a) post-surgical kidney dysfunction, b) prevalence of intraoperative hypotension, c) volumes of administered fluids, and d) length of hospitalization.

NCT ID: NCT02458859 Terminated - Wounds Clinical Trials

Trial of PICO Versus Standard Care in Chronic and Sub-acute Wounds

Start date: March 2012
Phase: N/A
Study type: Interventional

Randomised Controlled Trial of PICO (a portable Negative Pressure Wound Therapy) versus standard care in patients with chronic and sub-acute wounds. Sample size 100 patients to investigate Time to healing, health economic and patient reported outcomes.

NCT ID: NCT02457949 Terminated - Drug Use Clinical Trials

The Impact of Alternative Social Assistance Disbursement on Drug-related Harm

TASA
Start date: October 27, 2015
Phase: N/A
Study type: Interventional

This study evaluates whether altering the timing and frequency of social assistance disbursement reduces drug related-harms that increase on the days surrounding monthly synchronized government social assistance cheque issue.

NCT ID: NCT02456103 Terminated - Cystic Fibrosis Clinical Trials

Extension Study of Ataluren in Participants With Nonsense Mutation Cystic Fibrosis

Start date: August 31, 2015
Phase: Phase 3
Study type: Interventional

This is an open-label extension study for participants who completed a Phase 3, placebo-controlled study of ataluren in participants with nonsense mutation cystic fibrosis (nmCF) not receiving chronic inhaled aminoglycosides.