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Cancer clinical trials

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NCT ID: NCT02442635 Completed - Cancer Clinical Trials

Yoga During Chemotherapy Study

Start date: May 2015
Phase: N/A
Study type: Interventional

This proposal aims to expand non-pharmacologic options for the control of symptoms during chemotherapy using yoga practices. It is particularly focused on sleep disturbance with a secondary focus on fatigue.

NCT ID: NCT02442531 Completed - Cancer Clinical Trials

A Study of CriPec® Docetaxel Given to Patients With Solid Tumours

NAPOLY
Start date: August 2015
Phase: Phase 1
Study type: Interventional

The goal of this Phase1 clinical research study is to find the highest safe dose of CriPec® docetaxel that can be given in the treatment of patients with solid tumours.

NCT ID: NCT02437929 Completed - Pain Clinical Trials

Procedural Pain in Palliative Care: Prevalence, Intensity and Treatment

Start date: June 2015
Phase: N/A
Study type: Observational

This study aims to assess self reported procedural pain compared with background pain and evaluate pain intensity differences across six standard procedures. Besides, rescue and preventive treatments used to control procedural pain will be examined.

NCT ID: NCT02437227 Completed - Cancer Clinical Trials

A Phase I, First in Man Study to Evaluate the Safety and Tolerability of a panRAF Inhibitor (CCT3833/BAL3833)in Patients With Solid Tumours

PanRAF
Start date: April 15, 2015
Phase: Phase 1
Study type: Interventional

The study is a first in man, dose escalation study to evaluate the safety, tolerability and how the drug works in the body in patients with all solid tumours. The aim of this study is to determine the most effective dose of the study drug that can then be further investigated in patients with advanced melanoma.

NCT ID: NCT02432326 Completed - Cancer Clinical Trials

A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors

Start date: April 2015
Phase: Phase 1
Study type: Interventional

This is an open label, multi-center, phase 1 study of BBI608 and BBI503 administered orally in combination to patients with advanced solid tumors. The primary goal is to determine the safety, tolerability, and recommended phase II dose (RP2D) of the combination regimen.

NCT ID: NCT02426879 Completed - Cancer Clinical Trials

Esophagectomy for Patients With Esophageal Cancer and Cervical Lymph Node Metastases

Node
Start date: February 11, 2015
Phase: N/A
Study type: Interventional

There is no world-wide consensus on the oncological benefit versus increased morbidity associated with three field lymphadenectomy in patients with esophageal cancer and cervical lymph node metastases. In Asian countries, esophagectomy is commonly combined with a three field lymphadenectomy, including resection of cervical, thoracic and abdominal lymph nodes. However, in Western countries patients with cervical lymph node metastases are generally precluded from curative treatment.

NCT ID: NCT02411214 Completed - Cancer Clinical Trials

Decisional Process in Male Fertility Preservation

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

The survey analyses how to improve the decision-making process for fertility preservation in the pediatric population based on 1. patient and parent feelings about fertility preservation counselling 2. influence of the emotional state of patients and parents on fertility preservation acceptance 3. support of medical staff and family The study revealed that attention to the fertility preservation pathways was important for the satisfaction of patient's and parent's expectations

NCT ID: NCT02407977 Completed - Clinical trials for Cancer of the Gastrointestinal, Genitourinary or Gynecologic Systems

Real Time In-Vivo Body Surface Dosimetry for External Beam Radiation Therapy

Start date: November 13, 2015
Phase:
Study type: Observational

This is an observational study. This protocol will determine the feasibility of using a novel nano-material based fiber-optic dosimeter (nanoFOD) device, with dimensions less than 1 mm wide, to measure real-time, pin-point, in-vivo radiation dose given during external beam delivery of radiation therapy treatments.This new protocol is similiar in design to Pro00050297 with the significant difference being the monitoring will be performed during external baem radiotherapy.

NCT ID: NCT02405819 Completed - Cancer Clinical Trials

Patient and Provider Initiated Survivorship Care Planning

Start date: February 2015
Phase: N/A
Study type: Interventional

Objective: to describe and compare the implementation of two cancer survivorship care tools: (1) 'My Care Plan': a patient-initiated tool and (2) 'Survivorship Care Plan Builder': a provider-initiated tool. The results of this study will be used to (1) provide an initial assessment of the two survivorship care planning tools and (2) inform the design and conduct of a larger study.

NCT ID: NCT02404883 Completed - Cancer Clinical Trials

Decisional Conflict of Young Cancer Patients With Regard to Fertility Preservation

Fertionco
Start date: October 2014
Phase: N/A
Study type: Interventional

Women who are diagnosed with cancer during their reproductive lifespan might be confronted with impaired fertility. Nowadays a number of fertility preservation options are available. Decisions about whether and how to protect fertility have to be made in a very short time period, right after cancer diagnosis and before start of treatment. The psychological impact for patients is considerable. This project aims at developing a standardized decision-aid tool to support the decision-making process about fertility preservation in young cancer patients. It is designed as an online decision-aid tool. A web-based tool is perfectly designed for this target group and offers new possibilities providing flexible and individually tailored information. The aim of the study is to examine the benefits of the online decision-aid tool compared with standard counseling (usual care). Decisional conflict is measured immediately after counseling as well as one month later. One year after counseling, decisional regret is being evaluated additionally. If the decision-aid tool proves to be helpful and useful, the online design allows making it available for a wide range of concerned patients.