Clinical Trials Logo

Filter by:
NCT ID: NCT03305549 Terminated - Acute Kidney Injury Clinical Trials

Recovery After Dialysis-Requiring Acute Kidney Injury

RAD-AKI
Start date: September 29, 2017
Phase: N/A
Study type: Interventional

The Recovery After Dialysis-Requiring Acute Kidney Injury (RAD-AKI) Pilot Study is a 2-arm randomized clinical trial of hospitalized patients with dialysis-requiring acute kidney injury (RAD-AKI), comparing conventional thrice-weekly intermittent hemodialysis dialysis (control) to a "conservative dialysis strategy" in which hemodialysis is not continued unless specific metabolic or clinical indications for RRT are present. The overall hypothesis is that the current practice of thrice-weekly acute intermittent hemodialysis for AKI-D masks evidence of renal recovery and may actually delay or preclude recovery. The primary objective of this pilot study is to assess the safety and feasibility of the proposed intervention and study design.

NCT ID: NCT03305393 Terminated - Heart Failure Clinical Trials

Implementation of a Protocol Utilizing Adaptive CRT in a Normal AV Conduction, CRT Non-Response Population at Generator Replacement

Start date: June 11, 2017
Phase: N/A
Study type: Interventional

IMPROVE RESPONSE is a physician initiated research study. It is a prospective, non-randomized, multi-center, post-market, U.S. Cardiac Resynchronization Therapy (CRT) in heart failure (HF) observational study. The purpose of this clinical study is to test the hypothesis that market-released CRT devices, which contain the AdaptivCRT (aCRT) algorithm have an incremental benefit in improving CRT response in a chronic CRT non responder population with left bundle branch block (LBBB) and normal atrio-ventricular (AV) condition compared to CRT devices with traditional biventricular pacing delivery methods at generator replacement.

NCT ID: NCT03305081 Terminated - Contraception Clinical Trials

Patient Compliance With Long-Acting Reversible Contraception Administration

Start date: October 22, 2014
Phase: N/A
Study type: Interventional

This a randomized control trial to identify if patients who desire LARC are more likely to have success receiving the desired form of contraception if it is placed a) during the postpartum hospital stay, either in the immediate or early postpartum period, versus b) during the interval postpartum period as previously done.

NCT ID: NCT03305055 Terminated - Clinical trials for Posttraumatic Stress Disorder

RCT: Fentanyl Plus Ketamine Versus Fentanyl Alone for Acute Burn Pain

Start date: December 16, 2017
Phase: Phase 4
Study type: Interventional

The Ketamine for Acute Pain in Burns study is a randomized, double-blind, parallel group trial (RCT) with active control (usual care) contrasting the efficacy and safety of "Ketamine Plus Opiate-based usual care" (O+K) with the safety and efficacy of the "Current Standard of Care". THe current standard of care is an opiate medication alone, Fentanyl (Usual Care-Opiate (UC-O), dose/timing as per Burn Center protocol).

NCT ID: NCT03304184 Terminated - Quality of Life Clinical Trials

The Role of Biodentine in Class V Dental Lesions on Oral Health Related Quality of Life

Start date: September 28, 2017
Phase: Phase 3
Study type: Interventional

The study will compare two different dental materials on dental lesions near the gum line that cause chronic pain on oral health related quality of life.

NCT ID: NCT03303950 Terminated - Anemia Clinical Trials

Allogeneic Stem Cell Transplantation for Multiple Myeloma and Myelofibrosis

Start date: March 30, 2018
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well busulfan, fludarabine, donor stem cell transplant, and cyclophosphamide in treating participants with multiple myeloma or myelofibrosis. Drugs used in chemotherapy, such as busulfan, fludarabine, and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving chemotherapy before a donor stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. When the healthy stem cells from a donor are infused into the participant they may help the participant's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Giving busulfan and fludarabine before and cyclophosphamide after donor stem cell may work better in treating participants with multiple myeloma or myelofibrosis.

NCT ID: NCT03303794 Terminated - Anesthesia Clinical Trials

0.25% Bupivacaine Versus a Mixture of 0.25% Bupivacaine and 1.3 % Liposomal Bupivacaine in Patients Undergoing Tka

Start date: October 25, 2017
Phase: Phase 3
Study type: Interventional

Total knee and hip replacements are some of the most common orthopedic procedures that require aggressive postoperative pain management. This management helps us to improve clinical outcomes such as participation in early physical therapy, hospital discharge, and patient satisfaction. Based on the recent anatomical evidence and the investigator's knowledge of the complexity of the knee joint innervation the investigator proposes a new regional anesthesia technique that provides a complete sensory blockade and better analgesia while preserving the quadriceps strength and avoiding the potential for foot drop caused by inadvertent blockade of the common peroneal nerve.

NCT ID: NCT03303469 Terminated - Clinical trials for Hepatocellular Carcinoma

Hypoxic Changes in Hepatocellular Carcinoma (HCC) Following Trans Arterial Chemo Embolization and Stereotactic Radiation: Fluorine18 (18F) Fluoromisonidazole (FMISO) Imaging

Start date: October 30, 2017
Phase: Phase 2
Study type: Interventional

[18F] FMISO Positron Emission Tomography (PET) to determine hypoxia in patients with HCC treated with TACE.

NCT ID: NCT03303391 Terminated - Hypertension Clinical Trials

Using Intradialytic Blood Pressure Slopes to Guide Ultrafiltration

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

This study is an open label randomized clinical trial that comparing intradialytic blood pressure slope-based ultrafiltration prescriptions to standard care in the chronic fluid management of maintenance hemodialysis patients. It also includes a cross sectional component evaluating the associations between intradialytic blood pressure slopes ascertained over 2 week periods with measurements of extracellular water/body weight obtained with multifrequency bioimpedance spectroscopy.

NCT ID: NCT03302494 Terminated - Stroke Clinical Trials

WAveCrest Vs. Watchman TranssEptal LAA Closure to REduce AF-Mediated STroke 2

WAVECREST2
Start date: December 27, 2017
Phase: Phase 3
Study type: Interventional

The WAVECREST 2 trial is a prospective, multicenter, randomized, active controlled, clinical trial to evaluate the safety and effectiveness of the Coherex WaveCrest Left Atrial Appendage (LAA) Occlusion System.