Search Results 1601-1610 of 20736 for Informed consent
Ineligible to participate in a clinical trial using rMBCG or geographically unable to access a rMBCG clinical trial site. 4. Voluntary written informed consent ...
Capable of providing informed consent. Able and willing to follow study procedures in the view of the investigator. Confirmed diagnosis of ALS. Qualify for ...
Able to understand and give written informed consent and comply with study procedures. Exclusion Criteria: Patients meeting any of the following criteria ...
Informed of the investigational nature of the study and sign written informed consent. Willing and able to adhere to all study-related procedures, including ...
At the time of signing the informed consent at least 18 years of age and less than or equal to 89 years of age. Have known or highly suspected CNS pathology ...
Patients between the ages of 6 and 65 at the time of signing Informed Consent or Assent are eligible for the study. Patients must be obese, defined as BMI ...
Signed informed consent to participate in this study. Willing to participate in associated correlative science biomarker study; Serum creatinine ≤ 1.5 x ...
Patient has given voluntary written informed consent before performance of any study-related procedures not part of normal medical care, with the ...
Ability to provide informed consent; Current psychiatric inpatient (voluntary only) or outpatient treatment; Meets Diagnostic and Statistical Manual of Mental ...
Ability to provide informed consent and willingness to comply with protocol requirements; Life expectancy ≥ 6 months. Cohort A only: A diagnostic trans ...
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