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ePRO

Explore clinical trials studying ePRO. Study availability and eligibility vary by location and protocol.

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ePRO trial results

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Impact of Routine Electronic Patient-Reported Outcome (ePRO)Symptom Monitoring During Neoadjuvant Therapy in Patients withPancreatic Adenocarcinoma on Patient Experience and ClinicalOutcomes: A Prospective Pre-Post Implementation Study

NCT07829471

Conditions: Clinical Outcomes, Neoadjuvant Therapy, Pancreatic Adenocarcinoma, +2 more
Locations: UT MD Anderson Cancer Center Houston, Texas, United States

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