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MTN-016. Safety Monitoring and Reporting. Objectives. Apply safety assessment and reporting processes for both woman and their infants participating in MTN-016. Safety Monitoring and Reporting. Unanticipated problems/events related to MTN-016 PARTICIPATION :
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MTN-016 Safety Monitoring and Reporting
Objectives • Apply safety assessment and reporting processes for both woman and their infants participating in MTN-016.
Safety Monitoring and Reporting • Unanticipated problems/events related to MTN-016 PARTICIPATION: • Are the problem/event and participation in MTN-016 related in time? • Are the problem/event and participation in MTN-016 directly associated? • If yes, IoR to report • Appropriate IRB/EC • MTN-016 DAIDS Medical Officer (Dr. Jeanna Piper) • piperj@niaid.nih.gov
Safety Monitoring and Reporting What if an MTN-016 participant has what appears to be an SAE or EAE? • Any SAE or EAE that is considered reportable in the parent protocol should be reported via the safety reporting system utilized by the parent protocol.
Safety Monitoring and Reporting Women • All AEs related to woman as per ASPIRE reporting guidelines • Fetal loss NOT reportable as AE in ASPIRE • However, medical conditions resulting from or in fetal loss are reportable Infants • Congenital anomalies • Record as part of ASPIRE and MTN-016 Pregnancy Outcome • Complete ASPIRE and EAE reporting form
In the event of pregnancy loss, refer to the ASPIRE protocol & SSP Manual for reporting guidance. Fetal loss is NOT an adverse event in MTN-016 or ASPIRE.
Safety Monitoring and Reporting Social Harms Confirm whether related to MTN-016 participation or to the parent protocol Report on the relevant CRF Consult the MTN-016 team as needed
What is a Critical Event? Any unanticipated study-related incident likely to cause harm or increase risk of harm to participants or others or has a significant adverse impact on study outcomes or integrity. If incident appears to be a critical event, follow all applicable procedures in the DAIDS Critical Event Manual!