Clinical Trials Logo

Irradiation; Adverse Effect clinical trials

View clinical trials related to Irradiation; Adverse Effect.

Filter by:
  • None
  • Page 1

NCT ID: NCT05966363 Not yet recruiting - Clinical trials for Irradiation; Adverse Effect

Comparison of Cone Beam Irradiation Versus Multi-detector Scanner for Ear Imaging

ICSI
Start date: September 1, 2023
Phase:
Study type: Observational

The primary objective of this study is to compare the irradiation between Cone Beam and CT of the petrous bone. The primary endpoint is the measurement of equivalent doses per organ of interest (eyes, ears, thyroid and external genitalia). The investigators have set up a prospective monocentric study. The investigators will measure irradiation of these different organs using nanodots placed on the patient during imaging. The results of these measurements will be compared between Cone Beam (performed in the Besançon University Hospital ENT department for cochlear implant position checks) and CT (all indications combined).

NCT ID: NCT02824016 Completed - Clinical trials for Irradiation; Adverse Effect

Evaluation of Hypothyroidism Incidence After Breast Cancer Supraclavicular Irradiation

EPITHERM
Start date: February 2013
Phase: N/A
Study type: Interventional

Prospective, multicentric, comparative, non randomised, in current care. Primary objective: - To evaluate the incidence of hypothyroidism in breast cancer patients treated by radiotherapy including the supra-clavicular area over a period of 5 years (60 months). Secondary objectives : - To calculate the dose of irradiation received by thyroid gland during the treatment. - To compare the rate of incidence of hypothyroidism in women who received a supra-clavicular irradiation (group 1)and in those who did not (group 2). - To estimate and compare the rate of incidence of chronic thyroid lesions in the 2 groups. - To look for predictive factors of hypothyroidism de novo in group 1 women particularly regarding the dose-volume parameters. - To propose recommendations for the thyroid follow-up after supra-clavicular irradiation.

NCT ID: NCT02201563 Terminated - Clinical trials for Irradiation; Adverse Effect

Minocycline Therapy for Management of Adverse Radiation Effects

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

Stereotactic radiosurgery (SRS) is a well-established treatment for patients with metastatic brain tumors. Although SRS has a very high tumor growth control these interventions are associated with adverse radiation effects (ARE) in approximately 15 % of patients. The traditional approach, and still a mainstay, is the administration of a course of high dose anti-inflammatory corticosteroids. Currently there are no other effective oral neuroprotective agents in clinical practice which can improve outcomes of patients with ARE after radiosurgery for brain metastases. Minocycline, an antibiotic with a favorable adverse effect profile and pharmacokinetics, has been shown to have neuroprotective properties in experimental models of a variety of neurological diseases, as well as in human clinical trials. The investigators propose a single arm clinical trial, to evaluate the safety and feasibility of minocycline in improving ARE. This study will recruit 15 patients who will be treated with minocycline (100mg BID) for 3 months. This clinical trial has the potential to prove that minocycline therapy is safe in this patient population. In addition, positive results will provide preliminary evidence for its use in an array of radiosurgical indications.

NCT ID: NCT00904189 Terminated - Clinical trials for Irradiation; Adverse Effect

Measurement of the Radiation Dose Cuticles Using Electron Paramagnetic Resonance (EPR)

Start date: November 2007
Phase: N/A
Study type: Interventional

This study is to test the effectiveness a new method (called EPR dosimetry) that could be used to measure radiation doses to fingernails that occur as a result of unplanned exposure to radiation, such as might occur from the actions of terrorists, or from accidents.