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NCT ID: NCT01903473 Terminated - Clinical trials for Chronic Graft-Versus-Host Disease

Donor Regulatory T Cells Infusion in Patients With Chronic Graft-versus-host Disease (GVHD)

Start date: July 2013
Phase: Phase 2
Study type: Interventional

The immune system has offensive and defensive capacities. In bone marrow transplantation, offensive cells in the donor grafts may attack host's organs, leading to a complication known as Graft versus Host Disease (GVDH). At present, patients receive steroid treatment to combat this tricky situation. Nevertheless, some patients do not respond to this therapy. Recently, it has been shown that immune system cells having defensive capacities can help in preventing the occurrence of a GVDH. This study aims to evaluate if these protective cells together with a non-standard immunosuppressor can improve the clinical condition and suppress the activity of the offensive cells in the graft.

NCT ID: NCT01902381 Terminated - Clinical trials for Previously Treated Myelodysplastic Syndromes

CPI-613 in Treating Patients With Myelodysplastic Syndromes Who Failed Previous Therapy

Start date: August 2013
Phase: Phase 2
Study type: Interventional

This pilot clinical trial studies 6, 8-bis (benzylthio) octanoic acid (CPI-613) in treating patients with myelodysplastic syndromes who failed previous therapy. Sometimes when chemotherapy or biological therapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to treatment. 6, 8-bis (benzylthio) octanoic acid may interfere with the growth of tumor cells and may be an effective treatment for myelodysplastic syndromes that did not respond to previous therapy.

NCT ID: NCT01901354 Terminated - Acute Lung Injury Clinical Trials

Acute Lung Injury Ventilator Evaluation (ALIVE)

ALIVE
Start date: November 2013
Phase: N/A
Study type: Interventional

This study will compare two ventilator modes in mechanically ventilated patients with acute lung injury. Acute lung injury (ALI) is a condition in which the lungs are badly injured and are not able to absorb oxygen the way healthy lungs do. About 25% of patients who are ventilated get ALI. ALI causes 75,000 deaths in the US each year. Ventilators can be set to work in different ways, called modes. One mode, called ARDSNet, pumps a small amount of air into the patient's lungs and then most of the air is released prior to the next breath. Another mode, called Airway pressure release ventilation (APRV), keeps air in the lungs longer between breaths. Both of these modes are currently used at this hospital. The investigators think APRV may help patients with ALI, but we do not know for sure.

NCT ID: NCT01900795 Terminated - Clinical trials for Postsurgical Pain Due to Third Molar Extraction

An Analgesic Study to of V117957 for the Treatment of Postsurgical Pain Due to Third Molar Extraction

Start date: July 2013
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to assess the analgesic properties of an oral dose of V117957 4.5 mg aqueous suspension in the third molar extraction model

NCT ID: NCT01898377 Terminated - Clinical trials for Chronic Graft-versus-host Disease

Imatinib Mesylate and Mycophenolate Mofetil for Steroid-Refractory Sclerotic/Fibrotic cGVHD in Children

Start date: August 2013
Phase: Phase 2
Study type: Interventional

In this study we will combine mycophenolate mofetil and imatinib mesylate to treat steroid-refractory sclerotic/fibrotic type chronic graft-versus-host disease (GVHD) to see the response rate and to find the safety of combination.

NCT ID: NCT01898156 Terminated - Clinical trials for Phase 2 Portion : Small Cell Lung Cancer(SCLC)

Two-Part, Open-Label, Multi-Center, Phase 1/2 Study of BIW-8962 as Monotherapy in Subjects With Lung Cancer

Start date: July 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This Phase 1/2 study is designed to assess the following: safety and tolerability of BIW-8962, Dose Limiting Toxicities (DLTs), Maximum Tolerated Dose (MTD), Recommended Phase 2 Dose (RP2D) in Phase 1 in subjects with advanced/recurrent lung cancers or mesothelioma and preliminary efficacy in Phase 2 in subjects with advanced/recurrent Small Cell Lung Cancer.

NCT ID: NCT01897948 Terminated - Clinical trials for Measurement of Docosahexaenoic Acid Levels in Pre-school Children

The Effects of Feeding Different Levels of Docosahexaenoic Acid to Pre-School Children

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

This clinical trial will measure Docosahexaenic Acid (DHA) levels in the blood and evaluate the relation to cognitive outcomes.

NCT ID: NCT01897714 Terminated - Clinical trials for Relapsed and/or Relapsed-refractory Multiple Myeloma

Safety and Efficacy of Melflufen and Dexamethasone in Relapsed and/or Relapsed-Refractory Multiple Myeloma Patients

Start date: July 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The study will explore escalating doses of melflufen in combination with dexamethasone in small groups of patients to find the maximum tolerated dose of melflufen. That dose will then be used to determine the efficacy and safety profile of melflufen in combination with dexamethasone in a larger group of patients.

NCT ID: NCT01896973 Terminated - Clinical trials for Benign Prostatic Hyperplasia (BPH)

Safety and Initial Efficacy Study of the Vortx Rx for Treatment of Benign Prostatic Hyperplasia (US)

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

The HistoSonics' Histotripsy BPH Device, the Vortx Rx, is a portable ultrasound therapy device. The purpose of this study is to assess and monitor the performance of the Vortx Rx for initial safety and efficacy for the treatment of Benign Prostatic Hyperplasia.

NCT ID: NCT01896401 Terminated - Clinical trials for Percutaneous Closure of Artery Access Sites

InSeal Vascular Closure Device Clinical Study Protocol

VCD
Start date: February 2012
Phase: N/A
Study type: Interventional

The InSeal vascular closure device (VCD)is assessed as percutaneous closure of artery access sites for quick hemostasis and ambulation in patients who have undergone large bore endovascular catheterization procedures. The study hypothesis is that the VCD is safe and efficaient in achieving hemostasis in the study population.