Clinical Outcomes Registry (COR) Data Access
The Policy, Quality and Outcomes (PQO) subcommittee has developed a protocol that would allow members access to data from the COR registry. This data has been validated for clinical research. Please reference the 2020 SGO abstract for more information.
How to apply
Please complete the following research request form with as much information as possible. A member from the PQO subcommittee will reach out to you within two weeks of your submission with a data permission decision.
- Data Dictionary Terms
- Collection Form of Disease Sites
- Only SGO members can apply
- COR participants -no charge
- Non-COR participants $400 per disease site (i.e., cervix, endometrial, ovary)
Any questions, please contact SGO Staff Liaison, Jessica Oldham at firstname.lastname@example.org