Search Results 901-910 of 21184 for Informed consent
Signed informed consent. Exclusion Criteria: Biochemical relapse alone without clinically suspicious (i.e. no suspicious lesion on MRI of the prostatic bed) ...
Sufficient cognitive function to understand the expectations of the study and provide informed consent. Exclusion Criteria: Admitted from another hospital ...
Participants are able and willing to provide signed informed consent. Female patients of childbearing potential must have a negative pregnancy test result ...
Willing and able to provide informed consent to participate in the study at enrollment * and be followed at one of the participating MARS Consortium Sites ...
Written informed consent obtained; ≥ 21 and < 46 years of age at the time of the blood draw; Undergoing first cycle of ovarian stimulation for IVF or IVF ...
Unable to provide informed consent; Claustrophobia; Planning to move within 24 months of trial enrollment; Pregnant or breast-feeding. Participating Mayo Clinic ...
Signed informed consent. If taking pirfenidone or nintedanib, must be on stable dose for at least 6 weeks prior to enrollment visit. Confirmed rs3570920 TT ...
Be informed of the nature of the study and provide written informed consent before any study-specific procedures are performed. If female and of child ...
Willing to participate and give written informed consent. Exclusion Criteria: Any malignancy within past 5-years, except non-melanoma skin cancer, cervical ...
Inability to give informed consent. (BE patients only) History of prior endoscopic therapy for BE except a history of prior EMR of focal lesions without ...
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