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NCT ID: NCT00346112 Terminated - Clinical trials for Heart Patients After ICD Implantation

Rehabilitation, Quality of Life, and Exercise Tolerance in Patients With an ICD

Start date: June 2006
Phase: N/A
Study type: Interventional

RELAX-ICD Trial/Research Study; Quality of Life/Protocol No.P-KARE-01: A 3-month outpatient rehabilitation therapy and psychological counselling including informative talks with conventional therapy, by a cardiologist or general practitioner after implantation of an internal cardioverter defibrillator (ICD) in adult patients, whereby the effects of three different strategies are compared. Study hypothesis: the rehabilitation programme will be beneficial in the management of any psychological problems possibly as a result from the intervention, and will help to overcome anxiety, and contribute to improved quality of life.

NCT ID: NCT00345059 Terminated - Clinical trials for Advanced Non-Small Cell Lung Cancer

The DISTAL-2 Study: Docetaxel Alone or in Combination in Second-line Treatment of Advanced Non Small-Cell Lung Cancer

DISTAL-2
Start date: May 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the overall survival of patients with advanced non small cell lung cancer treated with docetaxel as single therapy versus docetaxel in combination with either gemcitabine or vinorelbine or in combination with capecitabine.

NCT ID: NCT00344786 Terminated - Clinical trials for B-Cell Chronic Lymphocytic Leukemia

Phase 1, Dose-Escalation Study of Oral CNF2024(BIIB021) in CLL

Start date: February 2006
Phase: Phase 1
Study type: Interventional

CLL dosing escalating study; daily dosing schedule; PK/PD safety

NCT ID: NCT00341523 Terminated - Stomach Neoplasms Clinical Trials

Early Detection of Esophageal Cancer

Start date: November 1, 2016
Phase:
Study type: Observational

Esophageal cancer is a common malignancy with a very poor prognosis. The principal reason for its poor prognosis is that most tumors are asymptomatic and go undetected until they have spread beyond the esophageal wall and are unresectable. Significant reduction in esophageal cancer mortality will require successful strategies to diagnose and treat more cases at earlier, more curable stages of disease. A successful early detection program will require an accurate, patient-acceptable screening test, confirmatory tests that can localize precursor and early invasive lesions, and one or more curative therapies that are acceptable to asymptomatic patients. This project includes five studies designed to evaluate techniques that may be useful in such an early detection program: 1. The Cytology Sampling Study will estimate and compare the sensitivity of several cytologic samplers for identifying biopsy-proven dysplasia and cancer of the esophagus. 2. The Mucosal Staining Study will evaluate whether mucosal straining can improve endoscopic localization of esophageal dysplasia and cancer. 3. The Endoscopic Staging Study will evaluate how accurately endoscopic techniques can stage dysplasia and early invasive cancer of the esophagus. 4. The Endoscopic Therapy Pilot Study will evaluate the feasibility, safety, acceptability and preliminary efficacy of endoscopic therapies for removing or ablating focal high-grade dysplasias and early invasive cancers of the esphagus. 5. The Chemoregression Study will evaluate the ability of oral chemopreventive agents to reduce progression or cause regression of low-grade squamous dysplasia of the esophagus. This project will be carried out in Linxian, China, a county with extraordinary rates of esophageal cancer and a correspondingly high prevalence of the asymptomatic precursor and early invasive lesions that are needed for these studies. The project will be a collaborative effort of investigators from NCI, the Cancer Institute of the Chinese Academy of Medical Sciences, and several U.S. universities.

NCT ID: NCT00338091 Terminated - Proteinuria Clinical Trials

Long-Term Renoprotection of Optimal Antiproteinuric Doses of Benazepril and Losartan in Chronic Renal Insufficiency

Start date: January 2002
Phase: N/A
Study type: Interventional

The primary goal of the trial was to evaluate whether the optimal antiproteinuric doses of benazepril (an ACE inhibitor) or losartan (an ARB), as compared with their conventional doses, can safely improve the long-term renal outcome in nondiabetic patients with proteinuria and chronic renal insufficiency. The second aim was to compare the long-term renal protection between benazepril and losartan at similar clinical setting.

NCT ID: NCT00334646 Terminated - Clinical trials for Nausea and Vomiting, Chemotherapy-Induced

Cyclophosphamide Drug Interaction Study In Cancer Patients

Start date: August 10, 2005
Phase: Phase 1
Study type: Interventional

This study is designed to evaluate the potential pharmacokinetic interaction between oral GW679769 and IV (intravenous) cyclophosphamide when administered to cancer patients.

NCT ID: NCT00333229 Terminated - Clinical trials for Primary Hormone Receptor Negative Breast Cancer in Premenopausal Women

A Study of Zoledronic Acid in the Prevention of Cancer Therapy-induced Bone Loss

Start date: March 2006
Phase: Phase 4
Study type: Interventional

Breast cancer and osteoporosis are two of the most frequent diseases in women. Estrogen may be associated with bone loss and the risk of breast cancer because of its potent effects on the mitotic activity of breast epithelium and on bone turnover. This study is will assess the safety and efficacy of Zoledronic acid 4 mg, given every 3 months over 24 months, in improving bone mineral density in premenopausal women with hormone receptor negative breast cancer and adjuvant chemotherapeutic treatment compared to placebo. This study is not recruiting patients in the United States.

NCT ID: NCT00332319 Terminated - Overactive Bladder Clinical Trials

Effects Of GW679769 On Bladder Nerve Function And Symptoms Of Overactive Bladder In Spinal Cord Injury Patients

Start date: January 2006
Phase: Phase 2
Study type: Interventional

This is a two-part study in which Part A will assess the effects of GW679769 after 1 dose on the function of the nerves that supply the bladder. The technique for measuring the nerves function is called Neurometry. Part B will assess the effect of repeat doses of GW679769 on the bladder nerve function. Part B will also assess the effects of the drug on overactive bladder symptoms using a three-day patient diary.

NCT ID: NCT00331877 Terminated - Clinical trials for Family of Dying Patient in the ICU

A Communication Strategy for Families of Patients Dying in the ICU

Start date: May 2005
Phase: N/A
Study type: Interventional

Decisions to limit life sustaining treatments are made for most patients dying in the ICU, usually with input from the family. The well-being of the family may be jeopardized by involvement in the decision-making process and bereavement. We evaluated the ability of a proactive communication strategy (family conference and providing family members with a bereavement information leaflet) designed to improve family well-being.

NCT ID: NCT00328185 Terminated - Clinical trials for Received Care at Children's Healthcare of Atlanta

Allograft Fibrosis Following Pediatric Cardiac Transplantation

Start date: January 2006
Phase: N/A
Study type: Observational

Transplantation is the preferred method of treating many forms of end-stage organ failure. While short-term results have improved, long-term outcomes remain inadequate. Myocardial fibrosis could potentially have an adverse effect on long-term cardiac function. We wish to study the degree of fibrosis to see if we can predict survival following pediatric heart transplantation.