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Clinical Trial Summary

This is a randomized trial of intensified post-discharge surveillance (Intervention Arm) versus standard post-discharge surveillance (Control Arm).


Clinical Trial Description

Eligible adult patients with probable or histologically/cytologically confirmed, primary or recurrent, malignant neoplasms (any stage) scheduled to undergo elective major cancer surgery at FCCC who meet eligibility criteria will be stratified by procedure type and randomized to the Intervention Arm or Control Arm. • Prior to discharge, patients who meet eligibility criteria at Second Registration will be confirmed for study eligibility and randomized. Patients in the Control Arm will receive standard post-discharge surveillance, as deemed appropriate/necessary by the surgeons caring for them at the time of hospital discharge. Patients in the Intervention and Control Arms will be monitored - Through PDD 30 for postoperative deaths and complications (as defined by ACS NSQIP) and/or adverse events (as defined by CTCAE) - Through the end of the index hospitalization for ICU admission, postoperative LOS, return to operating room, and discharge to home. - Through PDD 90 for hospital readmission, QOL, and receipt of anti-neoplastic therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05454280
Study type Interventional
Source Fox Chase Cancer Center
Contact Jason Castellanos, MD
Phone 215-728-3518
Email Jason.Castellanos@fccc.edu
Status Recruiting
Phase Phase 3
Start date October 14, 2022
Completion date November 1, 2028

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