[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100474160":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":40,"responsibleParty":55,"collaborators":26,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":26,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":26,"enrollmentInfo":66,"targetDuration":26,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":26,"overallStatus":43,"whyStopped":26,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Fox Chase Cancer Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Arm: Standard Perioperative Management","ACTIVE_COMPARATOR","Patients in the Control Arm will receive standard post-discharge surveillance (i.e., usual care).",[13],"Procedure: Standard post-discharge surveillance",{"label":15,"type":16,"description":17,"interventionNames":18},"Intervention Arm: Intensified Post-Discharge Surveillance","EXPERIMENTAL","Patients in the Intervention and Control Arms will be monitored\n\n* Through PDD 30 for postoperative deaths and complications (as defined by ACS NSQIP) and\u002For adverse events (as defined by CTCAE)\n* Through the end of the index hospitalization for ICU admission, postoperative LOS, return to operating room, and discharge to home.\n* Through PDD 90 for hospital readmission, QOL, and receipt of anti-neoplastic therapy",[19],"Procedure: Intensified post-discharge surveillance",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Intensified post-discharge surveillance","* TCC Nurse Televisit at post-discharge day 1 and 7\n* Televisit with APP\u002FResident\u002FFellow between post-discharge day 3-5\n* Referral for home health nursing evaluation upon discharge",[15],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard post-discharge surveillance","Patients in the Control Arm will receive standard post-discharge surveillance, as deemed appropriate\u002Fnecessary by the surgeons caring for them at the time of hospital discharge.",[9],[32],{"name":33,"affiliation":5,"role":34},"Jason Castellanos, MD","PRINCIPAL_INVESTIGATOR",[36],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","215-728-3518","Jason.Castellanos@fccc.edu",[41],{"facility":42,"status":43,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":26},"Fox Chase Cancer Center - Philadelphia","RECRUITING","Philadelphia","Pennsylvania","19111-2497","United States","US",{"type":50,"coordinates":51},"Point",[52,53],-75.16362,39.95238,{"lat":53,"lon":52},{"type":56,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100474160","phase-3-post-discharge-risk-based-management-in-patients-undergoing-high-risk-elective-major-cancer-operations-prs-ii-100474160",false,"NCT05454280","Post-Discharge Risk-Based Management in Patients Undergoing High-Risk Elective Major Cancer Operations (PRS II)","A Randomized Controlled Trial of Post-Discharge Risk-Based Management in Patients Undergoing High-Risk Elective Major Cancer Operations (PRS II)","First Registration Inclusion Criteria:\n\n* Age \\> 18 years at diagnosis\n* ECOG performance status 0, 1, or 2, defined as\n\nGrade ECOG 0 Fully active, able to carry on all pre-disease performance without restriction\n\n1. Restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g., light house work, office work\n2. Ambulatory and capable of all self-care but unable to carry out any work activities. Up and about more than 50% of waking hours\n\n   * Patients must have probable (i.e., clinically suspicious) or histologically\u002Fcytologically confirmed, primary or recurrent, malignant neoplasm, malignant neuroendocrine tumor, or carcinoma in situ (any stage).\n\nPatients undergoing major operations to resect or treat known or suspected malignancies of the head and neck, chest, abdomen, genitourinary tract, or extremities are eligible. Patients undergoing biopsies, outpatient procedures, superficial resections of cutaneous malignancies, or purely palliative operations are not eligible.\n\nThese procedures are commonly performed in patients with malignant neoplasms, malignant neuroendocrine tumors, or carcinomas in situ, and are commonly \"tracked\" by hospitals and cancer centers participating in the ACS NSQIP Procedure Targeted option because they are often associated with higher rates of postoperative morbidity and mortality (compared to other, less complex cancer procedures).\n\n* Patient must be scheduled for elective major cancer surgery (as listed in 4.1.4) at FCCC \\\u003C 30 days after First Registration.\n\nElective surgery is defined as:\n\n* Patient is scheduled to be brought from their home (or normal living environment) to FCCC on the day of the index surgery (or day prior as scheduled admission) AND\n* Surgery is not scheduled as urgent or emergent\n\n  * Ability to understand and willingness to sign a written informed consent and HIPAA consent document\n  * Geographical accessibility and willingness to return to FCCC for all preoperative and postoperative study assessments.\n\nFirst Registration Exclusion Criteria:\n\n* Any condition that might interfere with the subject's participation in the study, compliance with study requirements, or in the evaluation of the study results.\n\nSecond Registration Inclusion Criteria:\n\nA patient will be eligible for continued inclusion in this study only if ALL of the following criteria apply at the time of Second Registration (one to two days prior to anticipated discharge). No exceptions or waivers will be granted for patients who do not meet the eligibility criteria.\n\n* Post\n\n  * Elective (curative or palliative) major cancer surgery (as listed in 4.1.4 above) at the time of the index surgery (patient may have undergone more than one of these procedures) OR\n  * Elective surgical procedure(s) listed as an option (i.e., CPT code) in the Surgical Risk Calculator webpage (patient may have undergone more than one of these procedures)\n\nFor the purposes of this study, the procedure that was performed with the highest estimated risk of DSC (as predicted by the Surgical Risk Calculator) will be denoted at the time of Second Registration as the \"index procedure\" performed during the \"index surgery\".\n\n* Elective surgery \\\u003C 30 days after First Registration.\n\nSecond Registration Exclusion Criteria:\n\n* Status post elective surgical procedure(s) not listed as options in the Surgical Risk Calculator webpage. This includes patients whose scheduled procedure was suspended due to unexpected findings, such as carcinomatosis.","ALL","18 Years",{"count":67,"type":68},880,"ESTIMATED","INTERVENTIONAL",[71],"PHASE3","This is a randomized trial of intensified post-discharge surveillance (Intervention Arm) versus standard post-discharge surveillance (Control Arm).",[74,75],"Surgery","Cancer","2025-07-02",{"date":78,"type":79},"2025-07-08","ACTUAL",{"date":81,"type":79},"2022-10-14",{"date":83,"type":68},"2028-11-01",{"name":5,"class":6},1]