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Cancer clinical trials

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NCT ID: NCT02205853 Recruiting - Cancer Clinical Trials

Implementation of Physical Cancer Rehabilitation Programmes in a European Healthcare System.

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

The aim of this study is to develop and identify the most effective strategy to implement PCRPs into daily care. We want to assess the added value of a multi-faceted strategy compared with a single-faceted patient-directed strategy.

NCT ID: NCT02204137 Completed - Cancer Clinical Trials

Falls Risk Questionnaire in Older Adults With Cancer

Start date: August 2014
Phase: N/A
Study type: Observational

The purpose of this research study is to look at the use of a series of questionnaires evaluating risk for falls in order to collect information that might be used to develop a larger study aiming to recognize who is more at risk for falls and how to best intervene to prevent falls in older adults with cancer.

NCT ID: NCT02201823 Completed - Cancer Clinical Trials

Phase I/Ib Clinical Trial of ABTL0812 in Advanced Cancer Patients

Start date: February 2014
Phase: Phase 1
Study type: Interventional

Ability Pharmaceuticals promotes a clinical trial to determine the adequate dose of a new drug, ABTL0812, that will be administered orally daily to patients with advanced solid tumors.

NCT ID: NCT02201381 Withdrawn - Cancer Clinical Trials

Study of the Safety, Tolerability and Efficacy of Metabolic Combination Treatments on Cancer

METRICS
Start date: May 23, 2022
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the effectiveness of a regimen of selected metabolic treatments for patients with cancer in a real world setting and to conduct exploratory analysis on the relationship between the degree of response and changes in biochemical markers (such as glucose and lipid levels).

NCT ID: NCT02200172 Completed - Cancer Clinical Trials

The Preventative Role of Exogenous Melatonin Administration in Patients With Advanced Cancer Who Are at Risk of Delirium: a Feasibility Study

Start date: December 2014
Phase: Phase 2
Study type: Interventional

The purpose of this feasibility study is to inform a larger randomized, placebo-controlled, double blind, parallel-group, single-centre trial of an oral, daily administered single dose of melatonin to prevent delirium in patients with advanced cancer.

NCT ID: NCT02193503 Active, not recruiting - Cancer Clinical Trials

MVX-ONCO-1 in Patients With Solid Tumor

Start date: March 2014
Phase: Phase 1
Study type: Interventional

The objectives are to assess the safety and tolerability of 6 vaccine doses of MVX-ONCO-1, administered sub-cutaneously (injections and capsules implantations), in patients with advanced metastatic solid tumor in progression who are not or not any longer amenable to any standard therapy of their tumour disease.

NCT ID: NCT02191982 Completed - Cancer Clinical Trials

The Effect of Walking on Fatigue After Chemotherapy in Patients 65 and Older

S-PACT
Start date: June 2014
Phase: N/A
Study type: Interventional

This study will look at the impact of a self-directed walking program on post-chemotherapy survivors experiencing fatigue. It is hypothesized that the walking program will help lessen fatigue.

NCT ID: NCT02175823 Not yet recruiting - Cancer Clinical Trials

Health Status Evaluation for Cancer Survivors by Non-intrusive Sensing System

Start date: July 2014
Phase: N/A
Study type: Observational

To improve quality of life of elderly cancer survivors 1. Using physical activity and environmental sensing technology 2. Monitoring physiological indicators of cancer recurrence - Analyzing the patient's circadian rhythm, frailty and his/her vital sign. - Vital sign includes blood pressure, weight and hrv. 3. Collecting the patient information in real time - Giving alarm information to the patient, if any special cases our system found. - Giving circadian rhythm report to the patient. - Giving healthy report to the patient, collected from his/her vital sign.

NCT ID: NCT02175147 Recruiting - Cancer Clinical Trials

Patient-centred Integrated Palliative Care Pathways in Advanced Cancer and Chronic Disease

InSup-C
Start date: June 2014
Phase: N/A
Study type: Observational [Patient Registry]

Rationale: Palliative care integration in treatment pathways, palliative care networks and institutional collaborations in health services delivery seems a promising approach reducing fragmentation and discontinuity. Integrated Palliative Care (IPC) approaches in Europe are largely unknown and under-investigated. The investigators aim is to explore experiences of patients with advanced cancer, Chronic Obstructive Pulmonary Disease (COPD) and Chronic Heart Failure (CHF), family and professional caregivers within with IPC. This includes perceived quality of life, quality of care, burden/rewards of care giving, symptoms and collaboration between caregivers in the patient's care network. Objectives: To investigate how patients with advanced cancer, COPD and CHF, their family and professional caregivers within a selection of IPC initiatives in Belgium, Germany, Hungary, The Netherlands and United Kingdom experience care delivery in the last phase of disease. - To investigate what opinions patients and family caregivers have on the (continuity and) quality of care delivered - To investigate how patients rate their symptoms and quality of life - To investigate how family caregivers rate their burden / rewards of care giving - To investigate how the care network of the patient is organised with respect to the type, properties and quality of relationships between patients and family / professional caregivers Study design: Longitudinal multiple embedded case study. Study population: Adult patients with advanced cancer, COPD, and CHF under the care of IPC initiatives in five participating countries, their family and professional caregivers. The investigators aim to enroll up to 288 patients, 288 family caregivers and 192 professional caregivers in total. Study parameters: Experiences with IPC initiatives, quality of care, quality of life, perceived symptoms, perceived collaboration between professional caregivers, burden and rewards of care giving. Methods: Semi-structured interviews, patient diary, Social Network Analysis and the following questionnaires: Palliative care Outcome Scale; Canhelp Lite, Caregiver Reaction Assessment. Patients and family caregivers will be followed over 3 months at 4 consecutive contact points. The diary (containing two questions) will be kept weekly by patients. There will be group or individual interviews with professional caregivers. Analysis: The overall analysis will involve a synthesis of the qualitative and quantitative data. For more information see Detailed Description.

NCT ID: NCT02174679 No longer available - Clinical trials for Neuroendocrine Tumors

68Ga DOTATATE PET/CT in Neuroendocrine Tumors (Expanded Access)

Start date: n/a
Phase:
Study type: Expanded Access

To evaluate 68Ga-DOTATATE PET/CT for staging of patients with carcinoid, neuroendocrine tumors, medullary thyroid cancer and other cancers expressing somatostatin receptors.