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NCT ID: NCT02345772 Terminated - Clinical trials for HER2-positive Breast Cancer

Neoadjuvant Hormonal Therapy Combined With Chemoimmunotherapy

Neohttp
Start date: July 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Hormonal therapy administered before surgery in ER-positive and HER2-positive patients with breast cancer.

NCT ID: NCT02345460 Terminated - Clinical trials for Pancreatic Adenocarcinoma

Preoperative Folfirinox for Resectable Pancreatic Adenocarcinoma - A Phase II Study

Start date: September 2015
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well combination chemotherapy works in treating patients with pancreatic cancer before undergoing surgery. Drugs used in chemotherapy, such as irinotecan hydrochloride, oxaliplatin, leucovorin calcium, and fluorouracil (FOLFIRINOX), work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving more than one drug (combination chemotherapy) before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

NCT ID: NCT02345421 Terminated - Clinical trials for Lysosomal Acid Lipase Deficiency

A Study to Identify and Characterize LAL-D Patients in High-risk Populations

Start date: December 2014
Phase: N/A
Study type: Observational

The objective of this study is to determine the frequency of Lysosomal Acid Lipase Deficiency (LAL D) by lysosomal acid lipase (LAL) enzyme activity assay in patients who are considered to be at risk.

NCT ID: NCT02345369 Terminated - Hip Fractures Clinical Trials

Locked Versus Unlocked Set Screws in Intramedullary Fixation of Intertrochanteric Fractures

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

The purpose of this study is to look at the effect of locking or not locking a set screw when placing a rod and screws device in the thigh bone and hip to fix hip fractures. The set screw is an extra screw in the device that will not allow the screw that goes into the ball of the ball and socket joint in the hip to slide at all in relation to the rod in the thigh bone, which it goes through. It is not known whether it is better to lock the set screw (not allow sliding of the hip screw) or leave it unlocked (allow sliding of the hip screw). Participants in this study are patients with intertrochanteric hip fractures receiving standard care for this injury (lining the fracture up in a normal position and inserting a rod in the thigh bone with a screw that goes through the rod into the ball of the ball and socket of the hip). Patients who consent to participate will be randomized to one of two arms : 1. Set screw is unlocked or 2. Set screw is locked. Participants will all get standard postoperative care and standard postoperative xrays.

NCT ID: NCT02345330 Terminated - Clinical trials for Head and Neck Squamous Cell Carcinoma

Trial of pIL-12 Electroporation in Squamous Cell Carcinoma of the Head and Neck (IL12HNSCC)

Start date: May 21, 2015
Phase: Phase 2
Study type: Interventional

This study will assess the safety and effectiveness of ImmunoPulse IL-12® in treatment-refractory metastatic and unresectable squamous cell carcinoma of the head and neck (HNSCC). ImmunPulseIL12® is the combination of intrtumoral interleukin-12 gene (also known as tavokinogene telseplasmid [tavo]) and in vivo electroporation-mediated plasmid deoxyribonucleic acid [DNA] vaccine therapy (tavo-EP) administered using the OncoSec Medical System (OMS). Intratumoral tavo is a gene therapy approach to directly induce a pro-inflammatory response within a tumor to initiate and/or enhance anti-tumor immunity.

NCT ID: NCT02344537 Terminated - Clinical trials for Post Treatment Lyme Disease Syndrome

Meditation and Stretching for Post Treatment Lyme Disease Syndrome

LMS
Start date: November 1, 2015
Phase: N/A
Study type: Interventional

The investigators wish to conduct a preliminary study to examine the efficacy of meditation among patients with Post Treatment Lyme Syndrome (PTLDS). Specifically, the investigators will use the breathing, meditation, and stretching techniques common to Kundalini Yoga practice. The investigators plan to assess the degree in which this practice can reduce Post-Treatment Lyme Disease symptoms. Because fatigue and pain are so common among patients with PTLDS, the primary focus of this study will be fatigue and pain. Secondary outcomes will include cognitive complaints, physical and mental functioning, medical utilization, somatic symptoms, and psychopathology.

NCT ID: NCT02344342 Terminated - Heart Failure Clinical Trials

University of Michigan Advanced Heart Failure Tele-Monitoring and Flexible Diuretic Project

Manifold-HF
Start date: February 2015
Phase: N/A
Study type: Interventional

The proposed project is a 2x2 factorial designed study aimed at assessing the impact of 1) a home tele-monitoring system and 2) a flexible diuretic regimen among high risk heart failure patients in the University of Michigan Health System (UMHS).

NCT ID: NCT02343939 Terminated - Clinical trials for Acute Myeloid Leukemia

Entospletinib Monotherapy and in Combination With Chemotherapy in Adults With Acute Myeloid Leukemia (AML)

ENTO in AML
Start date: July 1, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This study will evaluate the efficacy, safety, and tolerability of entospletinib when administered as monotherapy or in combination with chemotherapy in adults with acute myeloid leukemia (AML).

NCT ID: NCT02343822 Terminated - Clinical trials for Lateral Epicondylitis

Multiple Platelet-Rich Plasma Lateral Epidondylitis Injections Versus a Single Platelet-Rich Plasma Injection

PRPLE
Start date: March 2015
Phase: N/A
Study type: Interventional

To determine the ideal dose of PRP for lateral epicondylitis. To see if 2 PRP injections are better than a single PRP injection or a saline injection to improve function and pain in patients with lateral epicondylitis.

NCT ID: NCT02343757 Terminated - Alzheimer Disease Clinical Trials

Alzheimer's Disease Imaging With PET/MRI - Beta-amyloid

Start date: October 2013
Phase: N/A
Study type: Interventional

The early detection of a preclinical AD or early stage of AD with amyloid imaging could improve the diagnosis and provide knowledge for better therapeutical approach by combining the best of imaging: structural MR sequences and newly FDA-approved biomarker for amyloid PET imaging, all these two techniques with their strengths in one machine. Specific Aims and Hypotheses can be summarized as follows: 1. To assess image quality and diagnostic performance of 18F-florbetapir (AMYVID) PET/MRI, including direct comparison to corresponding PET/CT images of the same patients. 2. To evaluate the incremental value of using 18F-florbetapir (AMYVID) in addition to 2-[F-18]-fluoro-2 deoxy-D-glucose (FDG) versus FDG alone. Does quantification of plaque burden correlate with degree of neuronal degeneration as depicted by FDG as well as with clinical severity? 3. To determine plaque burden quantitatively with 18F-florbetapir (AMYVID) in PET (form PET/CT and from PET/MR) using novel software developed specifically for these brain application; Computer-Aid Diagnosis for Dementia for amyloid imaging - CAD4D-amyloid