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NCT ID: NCT02405130 Withdrawn - Clinical trials for Percutaneous Coronary Intervention

The RESTORE-SIRIO Randomized Controlled Trial

RESTORE-SIRIO
Start date: April 2015
Phase: N/A
Study type: Interventional

Primary percutaneous coronary intervention (PPCI) is the preferred reperfusion strategy for treating acute ST-segment elevation myocardial infarction (STEMI). The main goals are to restore epicardial infarct-related artery patency and to achieve microvascular reperfusion as early as possible. No-reflow is the term used to describe inadequate myocardial perfusion of a given coronary segment without angiographic evidence of persistent mechanical obstruction of epicardial vessels and it refers to the high resistance of microvascular blood flow encountered during opening of the infarct-related coronary artery. Despite optimal evidence-based PPCI, myocardial no-reflow can still occur, negating many of the benefits of restoring culprit vessel patency, and is associated with a worse in-hospital and long-term prognosis. Several strategies have been tested to revert the no-reflow including the use of thrombectomy, glycoprotein IIb/IIIa inhibitors and the use of intracoronary adenosine, but none has been demonstrated to effectively counteract the phenomenon. The trial aims to show the effect of the administration of intracoronary adrenalin on myocardial reperfusion assessed by magnetic resonance in patients with STEMI undergoing PCI and with persistent coronary angiographic The Thrombolysis in Myocardial Infarction (TIMI) 0-1 flow during the interventional procedure after failure of standard therapy.

NCT ID: NCT02407184 Withdrawn - Human Microbiome Clinical Trials

Potential Restoration of the Infant Microbiome

PRIME
Start date: April 2015
Phase: N/A
Study type: Interventional

Understanding the microbiome's important role in human health, the investigators wish to determine how the development of the infant microbiome is impacted by delivery mode, comparing natural vaginal birth to scheduled C-sections. Investigators will look at the oral, nasal, skin, vaginal and fecal bacteria of 78 mothers and their infants from birth to age 1.

NCT ID: NCT02408042 Withdrawn - Lymphoma Clinical Trials

Study of Pembrolizumab With Chemotherapy in Patients With Advanced Lymphoma (PembroHeme)

Start date: April 2015
Phase: Phase 1/Phase 2
Study type: Interventional

To determine the recommended phase 2 dose of chemotherapy in combination with Pembrolizumab in subjects with advanced lymphoma and determine the complete response rate.

NCT ID: NCT02408081 Withdrawn - Depression Clinical Trials

Family Focused Nursing for Elderly Medical Patients

Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Family Focused Nursing are effective in the treatment of elderly medical patients with respect to prevalence of depression

NCT ID: NCT02409693 Withdrawn - Clinical trials for Otitis Media With Effusion (OME)

Retrospective Analysis of Perioperative Anesthetic Care and Analgesia Management of Patient Undergoing Bilateral Myringotomy With Tube Insertion

Start date: April 2015
Phase: N/A
Study type: Observational

This is a retrospective chart review. The purpose of this study is to retrospectively examine the use of perioperative analgesics on the incidence of postoperative pain and emergence delirium in patients undergoing bilateral myringotomy with tube insertion (BTI), as well as events associated with treatment including postoperative vomiting and time to discharge.

NCT ID: NCT02415257 Withdrawn - Clinical trials for Vestibular Schwannoma

Gentamicin Treatment Prior to Schwannoma Surgery - No Residual Function

Start date: April 2015
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine whether vestibular and postural compensation following schwannoma surgery is improved by ablating vestibular function prior to surgery, even if vestibular function is absent according to modern assessment techniques

NCT ID: NCT02422667 Withdrawn - Clinical trials for Arthroplasty, Replacement, Knee

iCORE: Collaborative Orthopedics Outcomes Registry

iCORE
Start date: April 2015
Phase:
Study type: Observational [Patient Registry]

The goal of this registry is to review the data collected and research ways to improve patient safety, quality of care, and medical decision-making, reduce medical spending, and help advance orthopedic science and bioengineering.

NCT ID: NCT02426021 Withdrawn - Clinical trials for Healthy Japanese and Caucasian Male Adults

Phase 1 Single Subcutaneous Dose Study of MLN1202

Start date: April 2015
Phase: Phase 1
Study type: Interventional

The objective of the study is to investigate the safety, pharmacokinetics, and pharmacodynamic effect of a single dose of MLN1202 in healthy Japanese male adults.

NCT ID: NCT02426385 Withdrawn - Cataract Clinical Trials

Comparison of Viusal Outcomes After Implantation of the POD 26% FineVision Toric (PhysIOL) and POD 26% Toric (PhysIOL)

Start date: April 2015
Phase:
Study type: Observational

The study is an observational non-randomised controlled study comparing the visual acuity after implantation of the POD 26% FINEVISION TORIC with respect to the POD 26% TORIC

NCT ID: NCT02429453 Withdrawn - Clinical trials for Intracranial Hemorrhage, Traumatic

FFP Versus PCC in Intracranial Hemorrhage

Start date: April 2015
Phase: N/A
Study type: Interventional

The goal of this study will be to determine whether PCC confers any benefits over FFP in traumatic and spontaneous intracranial hemorrhage with respect to multiple factors including time to correction, absolute international normalized ratio correction amount, cost, need for surgical intervention, and radiographic bleed expansion through a prospective, randomized control trial.