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NCT ID: NCT00696943 Terminated - Clinical trials for Metastasis to Brain of Unknown Primary

18F ML-10 for Early Detection of Response of Brain Metastases to SRS

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the potential of [18F]-ML-10 to serve as a non-invasive imaging tool for the early detection of apoptosis in brain metastases in response to radiation therapy, in patients subjected to stereotactic radiosurgery (SRS). Such early detection may improve clinical management of patients with brain metastases, as it may help early identification of non-responders, and subsequently potentially lead to optimization of radiation techniques such as the need for whole brain radiation therapy (WBRT), addition of brain penetrating chemotherapy or an early decision on referral of the patient with non-responsive lesions to surgery or to systemic chemotherapy. The experimental design of the present study aims to evaluate the potential of non-invasive PET examination with [18F]-ML-10, to provide the clinician with an assessment of response early in the course of treatment, via non-invasive molecular imaging of radiation-induced apoptosis. This information on tumor responsiveness is currently available only several weeks to months after completion of radiotherapy.

NCT ID: NCT00694967 Terminated - Clinical trials for Mid Trimester Cervical Shortening

A Randomized Trial of Cerclage Versus 17 α-Hydroxyprogesterone Caproate for Treatment of a Short Cervix

Start date: November 2003
Phase: N/A
Study type: Interventional

We hypothesized that weekly intramuscular injections of 17 hydroxyprogesterone caproate(17P) will reduce the number spontaneous preterm births prior to 35 weeks gestation when compared to cerclage therapy. The purpose of this study was to compare medical therapy with 17P to surgical therapy with transvaginal cerclage in patients with an ultrasound diagnosed short cervix and funnel in the mid-trimester.

NCT ID: NCT00694746 Terminated - Clinical trials for Non-alcoholic Fatty Liver Disease

Study of Fish Oil to Reduce ALT Levels in Adolescents

Start date: June 2008
Phase: Phase 1
Study type: Interventional

This trial will provide preliminary data to test the hypothesis that a six-month treatment period with fish oil for overweight adolescent with mild to moderate persistent elevation of ALT levels and presence of hepatic steatosis on CT-scan is safe and will result in decreased ALT.

NCT ID: NCT00694408 Terminated - Clinical trials for Evidence of Liver Transplantation

A Pilot Trial of Pediatric Liver Transplantation Without Steroids

Start date: June 2008
Phase: Phase 3
Study type: Interventional

Objective: The overall objective is to investigate whether a steroid free immunosuppressive regimen is as safe and effective as a steroid containing regimen following pediatric liver transplantation and whether it promotes tolerance.

NCT ID: NCT00691522 Terminated - Clinical trials for PRIMARY MALIGNANT and METASTATIC BRAIN TUMORS

Imaging Study of XERECEPT® Treatment for Peritumoral Brain Edema (PBE)

Start date: November 2008
Phase: Phase 2
Study type: Interventional

This is a phase II, multicenter, open-label, imaging study of hCRF in the reduction of PBE in patients with primary malignant or metastatic brain tumors. Approximately 30 to 60 patients will be assigned to 1 of 3 treatment groups and receive study drug for up to 28 days

NCT ID: NCT00690885 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

Interferon-alpha Treatment of Chronic Cough in Chronic Obstructive Pulmonary Disease and Idiopathic Pulmonary Fibrosis

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether lozenges containing interferon-alpha can reduce the frequency and severity of coughing in patients with chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF).

NCT ID: NCT00687674 Terminated - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Sorafenib, Lenalidomide, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma

Start date: August 2008
Phase: Phase 1
Study type: Interventional

RATIONALE: Sorafenib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Lenalidomide may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Sorafenib and lenalidomide may also stop the growth of cancer cells by blocking blood flow to the cancer. Giving sorafenib together with lenalidomide and dexamethasone may kill more cancer cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of sorafenib when given together with lenalidomide and dexamethasone and to see how well they work in treating patients with relapsed or refractory multiple myeloma.

NCT ID: NCT00687609 Terminated - Clinical trials for Attention Deficit Hyperactivity Disorder

Pilot Evaluation of Atomoxetine on Attention Deficit Hyperactivity Disorder (ADHD) Symptoms in Adolescents With Cannabis abusE

PEACE
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether atomoxetine is effective in reducing ADHD (Attention Deficit/Hyperactivity Disorder) symptoms in adolescents with ADHD and comorbid cannabis abuse.

NCT ID: NCT00685880 Terminated - Clinical trials for Thumb Carpometacarpal Joint Osteoarthritis

Prolotherapy Versus Steroids for Thumb Carpo-metacarpal Joint Arthritis

Start date: May 2008
Phase: N/A
Study type: Interventional

Arthritis of the base of the thumb is a common debilitating problem. It is believed that laxity (loosening) of the joint leads to worsening arthritis in this joint. This can be treated by securing the joint surgically or symptoms can be treated with hand therapy and/or injection of corticosteroids. Recently prolotherapy (sugar water) has been shown to decrease looseness of joints and also be helpful for hand and knee arthritis. We hypothesize that prolotherapy injections for thumb arthritis will be equally or more beneficial to the patients than steroids.

NCT ID: NCT00684931 Terminated - Clinical trials for Attention Deficit Disorder With Hyperactivity

Cerebellar Loops and Attention Deficit Hyperactivity Disorder (ADHD)

TDA/H
Start date: February 2008
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the integrity of connectivity between the neocortex and the cerebellum in the Attention Deficit Hyperactivity Disorder (ADHD). Fibers integrity will be measured using magnetic Resonance Imaging Techniques.