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Radiotherapy Side Effect clinical trials

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NCT ID: NCT03374592 Completed - Pain Clinical Trials

Volumetric Intensity Modulated Arc Therapy vs. Conventional Radiotherapy for Cancer Pain

Start date: July 7, 2014
Phase: N/A
Study type: Interventional

This study compares the use of conventional radiotherapy technique with volumetric intensity-modulated radiotherapy (VMAT) in the treatment of painful cancer metastases. Half of the patients will receive radiotherapy using a conventional technique, while the other half will receive their treatment using a the VMAT technique.

NCT ID: NCT03343236 Recruiting - Inflammation Clinical Trials

Nutrition and Inflammation in Patients With Head and Neck Cancer

Start date: November 1, 2015
Phase:
Study type: Observational

An estimated 1500 people in Sweden will annually be diagnosed with head and neck cancer (HNC). Five year survival is approximately 69%. Long-term sequelae are common and in particular nutritional problems and fatigue. Radiotherapy (RT) is the cornerstone of treatment, either as single modality treatment or combined modality treatment. RT can induce immune responses at the site of tumor. It has been demonstrated that RT can lead to a strong systemic immune response . We have previously shown that an increase of conventional measures of systemic immune response to RT varied significantly across individuals. We predict that local immune response plays a major role in the antitumor effect. We also predict that a strong systemic immune response contributes to malnutrition and influence on survival. And malnutrition may lead to a worse response to RT. The overall aim of this multicenter observational longitudinal study is to prospectively identify immunological and metabolic variables that affect the outcome of HNC patients. We will systematically investigate the local and systemic immune response induced by RT as well as explore alterations in metabolite composition induced by disease and treatment through global metabolite profiling. A platform for studies on immuno-metabolic changes in HNC patients has been established in the Uppsala-Orebro and Northern regions. Approximately 370 patients per year are eligible. Findings in this study can have implications on the development of personalized therapy in patients with HNC. The long-term benefit of the study will be the identification of measures for improved patient surveillance in order to improve the general and nutritional outcomes.

NCT ID: NCT03298204 Completed - Chemotherapy Effect Clinical Trials

Definitive (Chemo)Radiotherapy for Patients With Esophageal Cancer - 3JECROG R-01

Start date: June 1, 2017
Phase:
Study type: Observational

The aim of this observational study is to retrospectively collect survival data for 3000 primary esophageal cancer patients from multicenter between January 2000 to present. Based on a Cox model, we want to develope a nomogram that predicts local recurrence, distant metastases, and survival for patients treated with radiotherapy or chemoradiotherapy with or without chemotherapy.

NCT ID: NCT03109080 Completed - Clinical trials for Radiotherapy Side Effect

Olaparib & Radiation Therapy for Patients Triple Negative Breast Cancer (TNBC)

RadioPARP
Start date: July 24, 2017
Phase: Phase 1
Study type: Interventional

A Phase I of Olaparib with Radiation Therapy in Patients With Inflammatory, Loco-regionally Advanced or Metastatic TNBC (triple negative breast cancer) or Patient With Operated TNBC with Residual Disease.

NCT ID: NCT03071640 Completed - Cancer Clinical Trials

Improving Quality of Life and Function for Older Cancer Patients Receiving Radiotherapy

Start date: February 22, 2017
Phase:
Study type: Observational

This study is a first part of a larger project aiming at improving the following outcomes in older cancer patients receiving external beam radiation therapy (EBRT): quality of life, functioning and need for professional help (dependency). To achieve this, the investigators will develop and test a geriatric assessment (GA) with management (GAM) intervention targeting patients at risk of negative outcomes as defined. The problems and needs that older patients experience before, during and after EBRT are poorly described. Furthermore, although GA is the recommended approach to assess older cancer patients' vulnerability, very few studies have investigated its benefit and feasibility in a radiotherapy setting and there is no universal recipe for how an efficient GAM intervention should be applied in this setting. Before defining and testing an intervention, the investigators will therefore conduct an observational study addressing older patients >= 65 years referred for either palliative or curative EBRT. The main objectives are to identify patients at risk for negative outcomes, and to test the feasibility of GA in the community service and at a radiotherapy department.

NCT ID: NCT03061162 Recruiting - Stomach Neoplasms Clinical Trials

Pulsed Low Dose Rate Radiation Therapy for Gastric Cancer Patients With Peritoneal Metastasis

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

This phase II trial studies the side effects and response of pulsed low dose rate radiation therapy in treating gastric cancer patients with peritoneal metastasis.

NCT ID: NCT03060226 Completed - Clinical trials for Radiotherapy Side Effect

Prediction of Appearance of Late Cutaneous Side Effects After RadioTherapy

PAESCART
Start date: February 9, 2017
Phase: N/A
Study type: Interventional

Search for blood predictive marker (s) for cutaneous radiosensitivity

NCT ID: NCT02998619 Completed - Clinical trials for Radiotherapy Side Effect

Radiotherapy of Pelvic Lymph Nodes in High Risk Prostate Cancer - A Retrospective Analysis

Start date: December 2016
Phase:
Study type: Observational

Men with high risk prostate cancer who underwent radiotherapy of the prostate/seminal vesicles or underwent postoperative radiotherapy including pelvic lymph nodes between 2010 and 2016 are analyzed retrospectively. The aims are to estimate progression-free survival as well as toxicity according to CTCAE v4.03.

NCT ID: NCT02993978 Completed - Pediatric ALL Clinical Trials

Design and Evaluation of Care Environment and Technology at Pediatric Radiotherapy

DUMBO
Start date: August 2012
Phase: Phase 2
Study type: Observational

The purpose of the study is to evaluate the effect of changes in the care environment in pediatric radiotherapy. The definitions of the changes is a part of the study, and is constructed in collaboration with the institute of design at Umeå University. The implementation is however not part of the study, but done as part of Clinical routine. The study consist of two parts, where the first 1.5 years are a Control phase where the changes are designed and also function as a baseline period. The following 1.5 years are the case period where the Changes that are accepted for Clinical implementation are implemented. The impact of the changes are evaluated using surveys and interviews of both parents and children

NCT ID: NCT02986880 Completed - Clinical trials for Radiotherapy Side Effect

Effect of Type-A Botulinum Toxin in the Post-radiosurgical Neck Contractures

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

The main objective of the study is to estimate the efficiency and to determine the optimal dose of Botulinum toxin A, administered by intramuscular way in cervical spasms after radiotherapy, as well as the optimal sites for these injections. The concerned muscular groups are the sternocleidomastoid (SCM), the trapezius muscle and the splenius capitis.