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NCT ID: NCT00066417 Terminated - Leukemia Clinical Trials

Peripheral Stem Cell Transplant in Treating Patients With High-Risk Leukemia

Start date: n/a
Phase: Phase 2
Study type: Interventional

RATIONALE: Giving chemotherapy and total-body irradiation before a donor peripheral stem cell transplant helps stop the growth of cancer and abnormal cells and helps stop the patient's immune system from rejecting the donor's stem cells. When the stem cells from a related donor, that do not exactly match the patient's blood, are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. PURPOSE: This phase II trial is studying how well peripheral stem cell transplant works in treating patients with high-risk leukemia.

NCT ID: NCT00069732 Terminated - Obesity Clinical Trials

Study of Two Complementary and Alternative Medical Treatments for Maintenance of Weight Loss

Start date: n/a
Phase: Phase 2
Study type: Interventional

The goal of this study is to pilot test in a group of overweight-obese individuals the feasibility and acceptability and indications of efficacy of two CAM treatments, qigong, and acupressure-TAT, for improving long term maintenance of weight loss.

NCT ID: NCT00076401 Terminated - Leukemia Clinical Trials

A Study of Motexafin Gadolinium for the Treatment of Chronic Lymphocytic Leukemia (CLL)

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the drug motexafin gadolinium will be an effective treatment for patients who have chronic lymphocytic leukemia (CLL) that has come back after treatment or that has stopped responding to treatment.

NCT ID: NCT00080028 Terminated - Clinical trials for Head and Neck Cancer

Motexafin Gadolinium With Chemotherapy and Radiation Therapy for the Treatment of Advanced Head and Neck Cancer

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety of adding the investigational drug Motexafin Gadolinium to the standard treatment of radiation therapy and chemotherapy with drugs called 5-FU and cisplatin in patients with advanced head and neck cancer.

NCT ID: NCT00085761 Terminated - Pain Clinical Trials

Study of NGX-4010 for Treatment of Painful HIV-Associated Neuropathy

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if an investigational drug, NGX-4010 (high-concentration capsaicin patch), is safe, tolerable and effective in treating painful HIV-associated neuropathy.

NCT ID: NCT00088647 Terminated - Neoplasms Clinical Trials

Study Evaluating MST-997 in Advanced Malignant Solid Tumors

Start date: n/a
Phase: Phase 1
Study type: Interventional

The primary objective of this clinical research study is to evaluate the safety, tolerability, and maximum tolerated dose (MTD) of intravenous (IV) MST-997 formulated in Intralipid 20% administered on a weekly schedule to subjects with advanced malignant solid tumors.

NCT ID: NCT00089557 Terminated - Pain Clinical Trials

An Open-Label Extension Study of NGX-4010 for the Treatment of Neuropathic Pain

Start date: n/a
Phase: Phase 2
Study type: Interventional

This study is an open-label, multicenter, extension study for subjects who completed NeurogesX Study C111 and received treatment with NGX-4010 (Capsaicin Patch) within 12 weeks (up to +7days) before entry into Study C114

NCT ID: NCT00099879 Terminated - Clinical trials for Non-small Cell Lung Cancer

Study of BMS-275183 in Patients With Pre-treated Non-small Cell Lung Cancer

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this clinical research study is to learn if BMS-275183 can shrink or slow the growth of the cancer in subjects with non-small cell lung cancer (NSCLC). The safety of this treatment will also be studied.

NCT ID: NCT00100737 Terminated - Clinical trials for Non-Hodgkin Lymphoma

Comparing Interleukin-2 (IL-2) Combined With Rituximab (Rituxan) to Rituximab Alone in Subjects With Non-Hodgkin’s Lymphoma (NHL)

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether interleukin-2 given 3 times weekly for 8 weeks in combination with rituximab is effective and safe when compared to rituximab given alone in the treatment of follicular NHL subjects that have never received rituximab as a treatment and are refractory or relapsed after previous chemotherapy.

NCT ID: NCT00105859 Terminated - Spinal Cord Injury Clinical Trials

Preventing Pressure Ulcers in Veterans With Spinal Cord Injury (SCI)

Start date: n/a
Phase: N/A
Study type: Interventional

Pressure ulcers are a serious, costly, and life-long complication of spinal cord injury (SCI). Pressure ulcer prevalence has been estimated at between 17 and 33% among persons with SCI residing in the community. Epidemiological studies have found that 36-50% of all persons with SCI who develop pressure ulcers will develop a recurrence within the first year after initial healing (Carlson et al., 1992; Fuhrer et al., 1993; Goldstein, 1998; Niazi et al., 1997; Salzberg et al. 1998). Recurrence rates have ranged from 21% to 79%, regardless of treatment (Schryvers et al., 2000; Goodman et al., 1999; Niazi et al., 1997). Pressure ulcer treatment is expensive. Surgical costs associated with pressure ulcer treatment can exceed $70,000 per case (Braun et al., 1992). VA administrative (National Patient Care Database, NPCD) data indicate that 41% of inpatient days in the SCI population are accounted for by either primary or secondary diagnoses of pressure ulcers or 23% of SCI inpatient days if restricted to primary diagnoses of pressure ulcers. Pressure ulcer recurrence has been associated with many factors including previous pressure ulcer surgery (Niazi et al., 1997). Although little data exist describing the factors associated with recurrence following surgery, some investigators reported recurrence rates of 11%-29% in cases with post-operative complications and 6% to 61% in cases without post-operative complications (Mandrekas & Mastorakos, 1992; Relander & Palmer, 1988; Disa et al., 1992). In a retrospective study of 48 veterans with SCI, investigators reported a 79% recurrence rate following surgery (Goodman et al., 1999).