Adverse Events Reporting

As for any clinical study it is important to proactively monitor for adverse events, even mild ones, as part of ensuring the safety of participants.

During the study, the investigators and participating practitioners will be responsible for detecting and documenting events meeting the criteria and definition of an adverse event (AE) or serious adverse event (SAE).

An Adverse Event (AE) is any untoward medical occurrence (physical, psychological, social or economic), whether mild, moderate or severe, in a trial subject related to medical management, in contrast to complications of disease.

When an AE/SAE occurs, a Compass Trial Adverse Event Reporting Form should be completed and sent to the attention of: Prof Marion Saville, PO Box 178, Carlton South, VIC, 3053 or scan and email to Prof Marion Saville at [email protected]

If you need assistance in identifying an Adverse Event, or with completing the Form, please contact the Compass Hotline 1800-611-635.

Regular cervical screening is the best way to prevent cervical cancer in all women and people with a cervix

Self-collection is another option that is now available for cervical screening, and involves taking your own swab from the vagina. Find out more about self-collection here

Understand what happens if HPV is found on your Cervical Screening Test and what happens if more tests are needed.

ACPCC is a not-for-profit organisation and only charges patients the Medicare Schedule fee for pathology services, with only a small gap amount payable. 

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SELF COLLECTION

Screening Processes

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