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NCT ID: NCT03416946 Completed - Clinical trials for Osteoarthritis, Knee

Custom Cutting Block Instrument vs Regular Instrumentation Total Knee Replacement (TKR)

Start date: December 1, 2011
Phase: N/A
Study type: Interventional

To determine if the use of patient-specific custom cutting blocks for implantation of total knee components results in improved limb alignment and component positioning compared to regular instrumentation.

NCT ID: NCT03416270 Completed - Heart Failure Clinical Trials

ERtugliflozin triAl in DIabetes With Preserved or Reduced ejeCtion FrAcTion mEchanistic Evaluation in Heart Failure

ERADICATE-HF
Start date: June 28, 2018
Phase: Phase 2
Study type: Interventional

This study aims to elucidate the mechanisms whereby the SGLT2i "ertugliflozin" modifies cardiorenal interactions that regulate fluid volume and neurohormonal activation in patients with type 2 diabetes and heart failure (T2D-HF).

NCT ID: NCT03416179 Completed - Clinical trials for Leukemia, Myeloid, Acute

A Study Evaluating Intensive Chemotherapy With or Without Glasdegib or Azacitidine With or Without Glasdegib In Patients With Previously Untreated Acute Myeloid Leukemia

BRIGHT AML1019
Start date: April 20, 2018
Phase: Phase 3
Study type: Interventional

Glasdegib is being studied in combination with azacitidine for the treatment of adult patients with previously untreated acute myeloid leukemia (AML) who are not candidates for intensive induction chemotherapy (Non-intensive AML population). Glasdegib is being studied in combination with cytarabine and daunorubicin for the treatment of adult patients with previously untreated acute myeloid leukemia (Intensive AML population).

NCT ID: NCT03415997 Completed - Clinical trials for Contrast Media Dosing

Dosing Iodinated Contrast Media According to Lean vs. Total Body Weight

Start date: February 21, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of dosing iodinated contrast media according to a patient's total body weight vs. lean body weight. Participants will be randomized into 2 groups based on contrast dosing technique, and solid organ enhancement at uniphasic abdominal CT will be measured.

NCT ID: NCT03415958 Completed - Clinical trials for Malunion of Fracture of Clavicle

A Prospective Cohort of Displaced Adolescent Midshaft Clavicle Fractures

Start date: March 28, 2012
Phase: N/A
Study type: Observational

Outcomes for displaced midshaft clavicle fractures in adolescents are not defined. The current method of treatment for these fractures is non-operative management. There is recent Level 1 evidence in the adult literature to suggest that outcomes are superior when these fractures are managed surgically with open reduction and internal fixation.

NCT ID: NCT03415373 Completed - Clinical trials for Intradermal Injection

Clinical Evaluation of Healthy Subjects Receiving Intradermal Saline Using the Microneedle Adapter (Model UAR-2S)

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

Microdermics Inc. is a British Columbia-based Canadian incorporation primarily focusing on microneedle-based painless and effective drug delivery systems.The Microneedle Adapter (model UAR-2S) is a single-use disposable medical device intended to provide a mechanism for intradermal bolus fluid delivery when used with a standard syringe with a Luer-lock tip connection. The Microneedle Adapter consists of a single-use gold-coated metallic microneedle integrated within the microneedle adapter with fluidic connections to a standard Luer syringe mount. The primary function of the Microneedle Adapter is to guide the microneedle into the skin in a controlled manner for successful insertion passing the stratum corneum layer. The fluid loaded onto the syringe can then be injected precisely intradermally into the skin.The primary objective of this study is to evaluate the performance of the Microneedle Adapter in healthy subjects in 3 different injection sites. Pain perception of the Microneedle Adapter will be a key secondary outcome, compared with the control device.

NCT ID: NCT03414996 Completed - Clinical trials for Acute Coronary Syndrome

High-intensity Interval Training in Patients With Post-acute Coronary Syndrome

EXIT-IV
Start date: January 1, 2011
Phase: N/A
Study type: Interventional

To date, no studies have evaluated the safety or efficiency (improvement of maximal oxygen uptake [VO2peak]) of a high-intensity interval training (HIIT) program in post-acute coronary syndrome (post-ACS) patients. Heart rate variability (HRV) and recovery (HRR), QT dispersion (QTd) and ventricular arrhythmias are all indices associated with an increased risk of cardiac death. HIIT has been shown to improve these risk markers and be safe in coronary heart disease patients but not yet in post-ACS patients which are considered more at risks. The aim of this study was to compare a HIIT program to a moderate-intensity continuous exercise training (MICET) program on HRV, HRR, QTd parameters and occurrence of ventricular arrhythmias in post-ACS patients.

NCT ID: NCT03414983 Completed - Colorectal Cancer Clinical Trials

An Investigational Immunotherapy Study of Nivolumab With Standard of Care Therapy vs Standard of Care Therapy for First-Line Treatment of Colorectal Cancer That Has Spread

CheckMate 9X8
Start date: February 20, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

This purpose of this study is to evaluate nivolumab (BMS-936558) in combination with standard of care (SOC) chemotherapy with bevacizumab for the treatment of first-line metastatic colorectal cancer (mCRC).

NCT ID: NCT03414801 Completed - Allergic Rhinitis Clinical Trials

Red Maple Trials Cat Allergen Natural Exposure Chamber Validation in Cat-allergic Subjects

NEC
Start date: February 6, 2018
Phase: N/A
Study type: Interventional

To assess the reproducibility of the allergic response in the cat allergic subjects, measured as the change from baseline of the Total Nasal Symptom Score (TNSS) on the two challenge days.

NCT ID: NCT03413644 Completed - Leukemia-Lymphoma Clinical Trials

Evaluation of ClearLLab Leukemia and Lymphoma Panels

Start date: November 14, 2017
Phase:
Study type: Observational

Multi-center study of specimens from subjects presenting to the flow cytometry laboratory as part of their standard of care for hematological diseases work-up.