Patients with psychological, familial, social, or geographic factors that otherwise preclude them from giving informed consent, following the protocol, or potentially hamper compliance with study treatment and follow-up
Any psychological, familial, sociological, or geographic condition that may hamper compliance with the protocol and follow-up after treatment discontinuation
Presence of any other medical, psychological, familial, sociological, or geographic condition potentially hampering compliance with the study protocol Subjects who are participating in any other therapeutic clinical study (observational or registry trials are allowed).
Presence of any other medical, psychological, familial, sociological, or geographic condition potentially hampering compliance with the study protocol or would interfere with the study endpoints or the subject's ability to participate in the study in the judgement of the investigator
Patients with psychological or geographic conditions that prevent adequate follow-up or compliance with the study protocol.
Patient compliance and geographic proximity (as determined by the Principal Investigator) that allow adequate follow-up.
Patients with psychological or geographic conditions that prevent adequate follow- up or compliance with the study protocol.
Patients with psychological, familial, social, or geographic factors that otherwise preclude them from giving informed consent, following the protocol, or potentially hamper compliance with study treatment and follow-up
Patient compliance and geographic proximity that do not allow adequate follow-up
Patient compliance and geographic proximity that allow adequate follow-up
Absence of any psychological, familial, sociological or geographic condition that would potentially hamper compliance with the study protocol