Search Results 421-430 of 20645 for Informed consent

  1. Open-label Extension Study of Seralutinib in Adult Subjects With PAH (PROSERA-EXT) - Mayo Clinic

    Evidence of an informed consent document, signed and dated by the subject or his/her legal representative, indicating that the subject has been informed of ...

  2. Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil - Mayo Clinic

    Participation eligibility · An Institutional Review Board (IRB) approved informed consent is signed and dated by the patient prior to any study-related ...

  3. A Study To Evaluate The Efficacy And Safety Of Obinutuzumab In Patients With ISN/RPS 2003 Class III Or IV Lupus Nephritis - Mayo Clinic

    Signed Informed Consent Form. Age 18-75 years at time of signing Informed Consent Form. Ability to comply with the study protocol, in the investigator's ...

  4. A Study Evaluating AI-ECG Screening Following Cardiac Transplant - Mayo Clinic

    Patients ≥ 18 years of age. · History of receiving a heart transplant. · Scheduled for a endomyocardial biopsy and willing to sign informed consent.

  5. Genetic Investigations In Spontaneous Coronary Artery Dissection (SCAD) - Mayo Clinic

    Men and women able to give informed consent and complete a 2 page questionnaire; Diagnosis of one or more episodes of spontaneous coronary artery dissection ...

  6. A Study of Investigational Immunotherapy to Determine the Safety and Effectiveness of Nivolumab and Daratumumab, with or without Pomalidomide and Dexamethasone, in Patients with Relapsed/Refractory Hematologic Malignancies - Mayo Clinic

    Signed Written Informed Consent. Voluntary signed and dated IRB/IEC ... informed consent document. Exclusion Criteria: Target Disease Exceptions.

  7. A Study to Understand the Changes in Gastric Emptying in Response to the Endoscopic Sleeve Gastroplasty (ESG) - Mayo Clinic

    Ability to give informed consent; Women of childbearing potential (i.e., not post-menopausal or surgically sterilized) must agree to use adequate birth ...

  8. Study on Quality of Life and Resource Utilization in Chronic Pancreatitis - Mayo Clinic

    Patients unwilling or unable to provide informed consent. Note: Other protocol defined Inclusion/Exclusion Criteria may apply. Eligibility last updated 9/11 ...

  9. MediCool Protocol - Mayo Clinic

    Inability to give informed consent. Significant intra-cardiac thrombus; Subjects not eligible for or considered high risk for anticoagulation. Participating ...

  10. A Study of Quality of Life and Pain Control Before and After Endovascular Renal Denervation in Individuals with Refractory Kidney Pain - Mayo Clinic

    Unable to provide informed consent in the opinion of the PI or collaborator. Participating Mayo Clinic locations. Study statuses change often. Please contact ...