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NCT ID: NCT01761682 Terminated - Clinical trials for Lymphoblastic Lymphoma

Acute Lymphoblastic Leukemia Registry at Asan Medical Center

Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

The investigators would like to propose a prospective longitudinal observational cohort study for patients who will be diagnosed and/or treated for acute lymphoblastic leukemia at Asan Medical Center, Seoul, Korea, to use the acquired data for fundamentals of other retrospective analysis.

NCT ID: NCT01761201 Terminated - Clinical trials for Latent Tuberculosis Infection

"Efficacy and Safety of Levofloxacin vs Isoniazid in Latent Tuberculosis Infection in Liver Transplant Patients".

FLISH-ILT
Start date: January 2012
Phase: Phase 3
Study type: Interventional

A multicenter, prospective, non-inferiority, randomized and open clinical trial comparing levofloxacin with isoniazid in the treatment of latent tuberculosis infection in patients eligible for liver transplantation. Patients over 18 years of age on the waiting list for liver transplantation. Sample size: n=870 patients. HYPOTHESIS Levofloxacin treatment of latent tuberculosis infection, begun while on the waiting list for liver transplantation, is safer and not less effective than isoniazid treatment begun after transplantation when liver function is stable.

NCT ID: NCT01760941 Terminated - Clinical trials for Symptomatic Osseous Bone Lesions From Any Malignancy

Compassionate Same-Day Evaluation & Delivery of XRT for Bony Metastasis in Hospice Patients

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

This is a survey study to evaluate the feasibility and effectiveness of an affordable, $400 flat rate, same-day consultation, simulation, and delivery of a single fraction of palliative radiation therapy for patients with symptomatic bony metastatic disease who are currently enrolled in hospice. Treatment planning and delivery of palliative radiotherapy will utilize "standard of care" techniques.

NCT ID: NCT01760252 Terminated - Clinical trials for Metastatic Pancreatic Adenocarcinoma

Neoadjuvant CAPOXIRI Chemotherapy in the Treatment of Pancreatic Adenocarcinoma Protocol

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The combination of capecitabine, oxaliplatin, and irinotecan (CAPOXIRI) may be better than other combinations used to treat earlier stage pancreatic cancer patients with resectable (able to be cut out), borderline resectable, and locally advanced pancreatic adenocarcinoma. For subjects who can not obtain Capecitabine can be treated with 5-Fluorouracil (5-FU) along with Oxaliplatin and Irinotecan. Though all of the drugs in this study have been approved by the FDA, their combination is investigational. The purpose of this study is to evaluate the effects of CAPOXIRI (good and bad) on you and your cancer.

NCT ID: NCT01760161 Terminated - Clinical trials for Robotic Assisted Laparoscopic Surgery

Bilateral Dual Transversus Abdominis Plane Block for Robotic Assisted Laparoscopic Surgery

Start date: April 2014
Phase: N/A
Study type: Interventional

To evaluate the effects of bilateral dual transversus abdominis plane block on postoperative pain after robotic assited laparoskopic surgery and measure the plasma-level of ropivacain after the bilateral dual transversus abdominis plane block.

NCT ID: NCT01759914 Terminated - Clinical trials for Topical Corticosteroid-treated Dermatology Patients

Ocular Pressure in Steroid-treated Dermatology Patients

Start date: September 2012
Phase: N/A
Study type: Observational

Ocular hypertension and glaucoma are eye conditions associated with abnormally high fluid pressure in the eye (called intraocular pressure or IOP). If left untreated, the elevated IOP may eventually cause damage to the nerve of the eye and potential impairment of vision. The use of certain drugs has been identified as a risk factor for raised IOP, including various forms of administration of corticosteroids. Corticosteroids can also lead to cataract, which is clouding of the lens in the eye that can affect vision. In this research study, we would like to find out whether the use of corticosteroids in our dermatology clinic leads to raised IOP, in order to identify patients at risk and to allow them to be more closely monitored than others. It is important to identify those patients who have a corticosteroid-induced pressure rise early enough to prevent them from permanent glaucomatous visual loss.

NCT ID: NCT01759095 Terminated - Clinical trials for Any Event Leading to Hospitalisation

Multidrug Blister Pack Study

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

The purpose of this study is to determine the benefit of patients using a multidrug blister packs after discharged from an university hospital to their homes.

NCT ID: NCT01758575 Terminated - Clinical trials for Advanced or Metastatic Solid Malignancy

Clinical Evaluation of the Underlying Mechanisms of Targeted Therapy Related Toxicities

Start date: November 2012
Phase: N/A
Study type: Observational

Single center, non-randomized, interventional pilot study with feasibility analysis after enrollment of 20 patients. Adult patients with advanced solid tumors, for whom standard palliative treatment with targeted agents as monotherapy is indicated, including antiangiogenic tyrosine kinase inhibitors, EGFR inhibitors, mTOR inhibitors, BRAF inhibitors and ipilimumab.After feasibility analysis in the first twenty patients, twenty more patients will be included in each of the five drug cohorts. Biopsies will be performed to determine possible immunohistochemical and histopathological changes in normal tissue, possible immunomodulatory changes as expressed by Tcell phenotyping and cytokine profiling and to compare tissue (phospho) proteomic and kinase activity profiles before and during therapy and also at the development of toxicity.The main objective of this pilot study is to determine the biological impact of treatment with targeted agents at the systemic and local tissue level in relation to toxicity.

NCT ID: NCT01757691 Terminated - Clinical trials for Acute Demylelinating Optic Neuritis

Fingolimod (FTY720) in Acute Demyelinating Optic Neuritis (ADON)

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

To evaluate the efficacy and safety of fingolimod 0.5mg versus placebo in patients with suspected acute demyelinating optic neuritis (ADON) receiving standard steroid treatment

NCT ID: NCT01757314 Terminated - Clinical trials for Surgeries Requiring Arterial Lines

Comparing Palpation Guided and Ultrasound Guided Arterial Line Placement

Start date: October 2012
Phase: N/A
Study type: Observational

When surgery is performed under general anesthesia, a catheter is placed in a vein to administer drugs and saline. During major operations, an additional catheter is placed in an artery in order to measure the blood pressure closely and withdraw blood samples at frequent intervals for various laboratory tests. This arterial catheter is usually placed by feeling the patient's artery at the wrist and inserting the guide-needle in a blind fashion. This procedure, at times, leads to delays and failures due to an inability to feel the arterial pulsation well either due to the patients' anatomy or the anesthetic effect. This study will determine whether training Anesthesiology Residents in the use of ultrasound technology and its application in identifying an artery can prevent the problems associated with the conventional palpation technique. Our finding will lead to better and safer anesthetic management of patients presenting for a major surgical procedure. Furthermore, the finding will help us in introducing the education and training of ultrasound-guided arterial catheter placement in our Residency Program. The investigators propose to follow anesthesia residents over a course of 3 years assessing their skill level for both palpation and ultrasound technique.