Patients who are otherwise felt unable to comply with the protocol, in the opinion of the investigator
Patients unable to comply with instructions for DIBH
Unwilling or unable to provide written informed consent, comply with study requirements, or be available for follow-up assessments
Patients unable to comply with the protocol
The subject or guardian is unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up and research tests.
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up, and research tests.
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, long-term follow-up, and research tests.
Unable to comply with the requirements of the protocol, or unable to provide adequate informed consent in the opinion of the principal investigator
Patients who are not available for follow-up assessments or unable to comply with study requirements
Unable to comply with protocol
Unstable psychiatric disorder that would render the patient unable to comply with study requirements.
Unable to comply with study requirements in the opinion of the Investigator.
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up and research tests
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up, and research tests
Unable to provide informed consent or, in the opinion of the Principal Investigator, comply with the protocol.
Patients who, for medical or other reasons, are unable to comply with the study procedures
Unable to comply with the requirements of the protocol, or unable to provide adequate informed consent in the opinion of the principal investigator
Patients unable to comply with the protocol as judged by the investigator.
Patient unable to consent or comply with study guidelines
Is unable to comply with study requirements
Unable to give informed consent or comply with clinical trial requirements
The patient or parent(s)/guardian(s) is/are unable to comply with the study visit schedule and other protocol requirements, in the opinion of the investigator.
Patients who, in the opinion of the investigator, are unable to comply with the requirements of the study protocol are not eligible
Patients who are not available for follow-up assessments or unable to comply with study requirements
Patient unable to comply with the protocol, in the opinion of the investigator.
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up, and research tests
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up and research tests
Patients unable to comply with the protocol
Unable to comply with treatment with the NovoTTF-100A device
A subject who, in the opinion of the sponsor-investigator will be uncooperative or unable to comply with study procedures
Unable to comply with study requirements in the opinion of the Investigator.
Patient is unable to comply with the requirements of the study.
Patients unable to comply with the protocol
Unable to comply with the protocol for any reason
Any patients who are unable to comply with the study procedures as determined by the study investigators
Unable to comply with protocol and/or not available for follow-up assessments
Has any other condition or prior therapy that in the opinion of the Investigator would make the patient unsuitable for the study and/or unable to comply with requirements for follow-up visits.
Any patient, in the opinion of the investigator, who is unable or unlikely to comply fully with the study requirements or procedures for any reason
Unable to comply with the protocol for any reason
Patient unable to comply with the treatment protocol including appropriate supportive care, follow-up and research tests
Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up and research tests
A subject who, in the opinion of the sponsor-investigator will be uncooperative or unable to comply with study procedures
If, in the opinion of the Investigator, the patient is deemed unwilling or unable to comply with the requirements of the Study
Individuals who are unable to comply with photosensitivity precautions
Unable to provide informed consent or high risk that patient may not comply with\n             protocol requirements (i.e. due to health and/or participation in other research\n             studies).