The ImPreSS Trial: Pharmacogenomic Decision Making at Time of Surgery
Launched by UNIVERSITY OF CHICAGO · Oct 31, 2018
Trial Information
Current as of May 20, 2025
Recruiting
Keywords
ClinConnect Summary
The ImPreSS Trial is a study looking at how genetic information can help doctors choose the best medications for patients undergoing elective surgeries at The University of Chicago. The trial involves adults aged 18 and older who are scheduled for these surgeries. Before the surgery, participants will provide a blood sample to test for specific genetic markers that can influence how they respond to certain drugs. This information will then be shared with their doctors through a secure online system called the Genomic Prescribing System (GPS), which aims to improve medication safety and effectiveness.
Participants will first take part in a six-month period where about 100 patients' genetic results will be made available to their healthcare providers. After this, patients will be randomly assigned to one of two groups: one group will have access to their genetic information when deciding on medications, while the other group will follow the current standard practices without this information. This trial is open to adults who are eligible for elective surgery, but those with specific conditions, like active leukemia or those considering organ transplants, cannot participate. Overall, the trial aims to enhance decision-making for medication during surgery using personalized genetic insights.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adult patients who have planned elective surgical procedures at the University of Chicago
- • Must be aged 18 years or older
- Exclusion Criteria:
- • Patients who have undergone, or are being actively considered for, liver or kidney transplantation
- • Patients with known active or prior leukemia.
- • Inability to understand and give informed consent to participate.
About University Of Chicago
The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
Patients applied
Trial Officials
Peter O'Donnell
Principal Investigator
University of Chicago
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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