IRB Closure Report

Please complete the following questions regarding your research study or quality improvement project since the last summary you submitted. If this is the first protocol summary about this project, please include information about your entire sample.

Principal Investigator Principal Investigator First Last
IRB Protocol Number
Email

Confirm Email Address
Project Title
1. Total number of subjuects accrued:
Caucasian
African-American
Native American
Asian or Pacific Islander
Other
Male
Female
2. Number of vulnerable subjects accrued:
Pregnant women
Incarcerated persons
Mentally disabled
Children
Economically disadvantaged
Educationally disadvantaged
Students who you advise or mentor
Students in your courses
3. Unanticipated problems or adverse events. If (1) severe, (2) related to your study, and (3) unanticipated, complete the Adverse Events Reporting form.

3. Unanticipated problems or adverse events. If (1) severe, (2) related to your study, and (3) unanticipated, complete the Adverse Events Reporting form. No unanticiapted problems ore advers events occured Adverse events occurred at expected rate, as described in original or amended protocola applicaiton Unanticipated adverse events occurred.
Date Adverse Event form filed with IRB
4. How many subjects withdrew from the study/project?
4.a. Please describe the reasons why the subjects withdrew:
5. Provide a brief paragraph describing your results:
6. Draw your signature into the box below.

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Full Name

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