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NCT ID: NCT03120078 Terminated - Adenomyosis Clinical Trials

A Prospective Study of Diagnostic Accuracy of Ultrasound

Start date: June 1, 2017
Phase:
Study type: Observational

Prospectively-Patients undergoing a hysterectomy for abnormal uterine bleeding (AUB) or pelvic pain will be enrolled in the study, will get pelvic ultrasound at the ultrasound clinic. An ultrasound will be obtained as part of the required clinical assessment before the patient undergoes a hysterectomy. The ultrasound images will be reviewed using Viewpoint reporting system-various sonographic features of adenomyosis will be reported detailed, including pelvic pathology, pelvic congestion syndrome etc. The histopathological examination will be done by assigned pathologist for accurate mapping/localizing the adenomyosis (appropriate section of uterus to defining localized versus generalized adenomyosis) on all patients diagnosed with adenomyosis on ultrasound. The ultrasound will be correlated with histopathology(which is the gold standard for diagnosis of adenomyosis). Scoring system for adenomyosis based on various sonographic features/clinical symptoms and their confirmation with histopathology will be developed.

NCT ID: NCT03119662 Terminated - Clinical trials for Chronic Kidney Diseases

A Study to Explore the Renal Safety of Visipaque Injection 320 mgI/mL in Patients With Chronic Kidney Disease

Start date: February 8, 2018
Phase: Phase 4
Study type: Interventional

This parallel-group, randomized, placebo-controlled study will examine the incidence and severity of acute kidney injury (AKI) in patients with chronic kidney disease (CKD) stage III/IV following an i.v. injection of iso-osmolar iodinated contrast material iodixanol (Visipaqueâ„¢ Injection 320 mgI/mL), as compared with patients who received saline and underwent a non-enhanced CT (NECT) and duplex ultrasound (US) during their scheduled post-EVAR surveillance imaging.

NCT ID: NCT03119571 Terminated - Clinical trials for Ventricular Fibrillation

ACCESS to the Cardiac Cath Lab in Patients Without STEMI Resuscitated From Out-of-hospital VT/VF Cardiac Arrest

Start date: December 12, 2017
Phase: N/A
Study type: Interventional

To determine if survival to hospital discharge with good neurological outcome for adults ages 18-75 who are resuscitated from out-of-hospital VT/VF cardiac arrest without clinical signs of a heart attack do better by going straight to the cardiac catheterization laboratory or admitted to the intensive care unit for evaluation. The investigators think a large portion of resuscitated patients presenting with VT/VF have ischemic heart disease which is the cause for the arrest. And prompt access to the cardiac catheterization laboratory to reverse the blocked artery will improve survival with good neurological outcomes.

NCT ID: NCT03119467 Terminated - Lymphoma Clinical Trials

Safety and Efficacy Study of RP4010, in Patients With Relapsed or Refractory Lymphomas

Start date: May 11, 2017
Phase: Phase 1
Study type: Interventional

A Phase I/Ib, Study to Evaluate Safety and Efficacy of RP4010, in Patients with Relapsed or Refractory Lymphomas

NCT ID: NCT03119428 Terminated - Metastatic Cancer Clinical Trials

A Study of OMP-313M32 in Subjects With Locally Advanced or Metastatic Solid Tumors

Start date: May 2, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of OMP-31M32 as a single agent or in combination with nivolumab. OMP-313M32 is an experimental anti-TIGIT antibody that was developed to block TIGIT from binding PVR allowing the body's T-cells to destroy cancer cells.

NCT ID: NCT03119064 Terminated - Glioblastoma Clinical Trials

BrUOG 329 Onivyde & Metronomic Temozolomide in Recurrent Glioblastoma

329
Start date: November 30, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

New treatments are greatly needed for patients with recurrent glioblastoma. Metronomic temozolomide is a standard treatment option but has, at best, modest activity. The nanoliposomal irinotecan may be much more active than the parent compound irinotecan since nanoliposomal irinotecan's ability to cross the blood brain barrier is improved. This phase I study will establish the MTD of the combination of nanoliposomal irinotecan in combination with temozolomide safety and preliminary clinical efficacy of the combination of nanoliposomal irinotecan and metronomic temozolomide.

NCT ID: NCT03118700 Terminated - Exercise Clinical Trials

Central Hemodynamic Exercise Responses Study

CHeER
Start date: March 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the acute effect of continuous and aerobic interval exercise on postexercise central BP response in men with an elevated blood pressure.

NCT ID: NCT03118544 Terminated - Clinical trials for Chronic Total Occlusion of Coronary Artery

REduction of Contrast Via DyeVert Used in CTO Procedures

REDUCe
Start date: March 26, 2017
Phase:
Study type: Observational [Patient Registry]

The is an observational, prospective study to evaluate the effect of the DyeVert System on contrast volume administration in patients undergoing clinically-indicated chronic total occlusion (CTO) percutaneous coronary intervention (PCI)

NCT ID: NCT03118479 Terminated - Clinical trials for Hypogonadotropic Hypogonadism

Effect of Varying Testosterone Levels on Insulin Sensitivity in Men With Idiopathic Hypogonadotropic Hypogonadism (IHH)

Start date: May 2010
Phase: Phase 1
Study type: Interventional

The investigators are doing this research study to look at the relationship between testosterone (the main sex hormone in men) and insulin (the hormone that controls blood sugar levels) in men with Idiopathic Hypogonadotropic Hypogonadism (IHH). The investigators hypothesize that normalizing testosterone levels in men with IHH enhances insulin sensitivity, reduces visceral fat, increases lean body mass, and improves the lipid profile.

NCT ID: NCT03118375 Terminated - Clinical trials for Conductive and Sensorineural Hearing Loss

Super Power in BAI

Start date: April 12, 2017
Phase:
Study type: Observational

The purpose of this study is to assess the benefit of new super-power bone-anchored hearing aid (BAHA) processors in BAHA users. BAHAs are able to help people with mixed/conductive and single-sided hearing loss when they are unable to use or receive limited benefit from traditional hearing. Until recently, BAHAs were only recommended to people with up to a moderate hearing loss. New super-power BAHA processors may be able to help people who previously were not candidates for BAHAs or received limited benefit from them. The information collected in this study may lead to improved evaluation of and expanded treatment options for people considering BAHA. Different types of hearing tests will be used to compare the devices.