[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100628070":3},{"organization":4,"armGroups":7,"interventions":36,"overallOfficials":123,"centralContacts":128,"locations":137,"responsibleParty":155,"collaborators":115,"id":157,"slug":158,"hasResults":159,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":115,"eligibilityCriteria":163,"healthyVolunteers":159,"sex":164,"minAge":165,"maxAge":115,"enrollmentInfo":166,"targetDuration":115,"studyType":169,"phases":170,"briefSummary":173,"conditions":174,"keywords":115,"overallStatus":139,"whyStopped":115,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":185},{"fullName":5,"class":6},"Mayo Clinic","OTHER",[8,20,25,30],{"label":9,"type":10,"description":11,"interventionNames":12},"Phase I (EndoPAT, ECG, Holter monitoring, blood sample)","EXPERIMENTAL","Patients undergo EndoPat, ECG, Holter monitoring for 48 hours, and blood sample collection during their SOC 5-FU infusion (any time from 2 hours after start to end of infusion) and 12-36 hours post-infusion or SOC capecitabine infusion 5-8 days after starting cycle 1 and 5-8 days after completing cycle 1, before beginning the next cycle of treatment.",[13,14,15,16,17,18,19],"Procedure: Biospecimen Collection","Drug: Capecitabine","Procedure: Electrocardiogram","Drug: Fluorouracil","Device: Holter Monitoring","Other: Medical Device Usage and Evaluation","Other: Questionnaire Administration",{"label":21,"type":10,"description":22,"interventionNames":23},"Phase II arm I (Isosorbide mononitrate)","Patients receive isosorbide mononitrate PO QD for 7-12 days on study. Patients also undergo EndoPat, ECG, Holter monitoring for 48 hours, and blood sample collection on study.",[13,15,17,24,18,19],"Drug: Isosorbide Mononitrate",{"label":26,"type":10,"description":27,"interventionNames":28},"Phase II arm II (Diltiazem hydrochloride)","Patients receive diltiazem PO QD for 7-12 days on study. Patients also undergo EndoPat, ECG, Holter monitoring for 48 hours, and blood sample collection on study.",[13,29,15,17,18,19],"Drug: Diltiazem Hydrochloride",{"label":31,"type":32,"description":33,"interventionNames":34},"Phase II arm III (Placebo administration)","PLACEBO_COMPARATOR","Patients receive placebo PO QD for 7-12 days on study. Patients also undergo EndoPat, ECG, Holter monitoring for 48 hours, and blood sample collection on study.",[13,15,17,18,35,19],"Drug: Placebo Administration",[37,46,54,61,69,94,103,111,116,119],{"type":38,"name":39,"description":40,"armGroupLabels":41,"otherNames":42},"PROCEDURE","Biospecimen Collection","Undergo blood sample collection",[9,21,26,31],[43,44,45],"Biological Sample Collection","Biospecimen Collected","Specimen Collection",{"type":47,"name":48,"description":49,"armGroupLabels":50,"otherNames":51},"DRUG","Capecitabine","Given IPO",[9],[52,53],"Ro 09-1978\u002F000","Xeloda",{"type":47,"name":55,"description":56,"armGroupLabels":57,"otherNames":58},"Diltiazem Hydrochloride","Given PO",[26],[59,60],"Cardizem","Diltiazem HCl",{"type":38,"name":62,"description":63,"armGroupLabels":64,"otherNames":65},"Electrocardiogram","Undergo ECG",[9,21,26,31],[66,67,68],"ECG","EKG","Electrocardiograms",{"type":47,"name":70,"description":71,"armGroupLabels":72,"otherNames":73},"Fluorouracil","Given IV",[9],[74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93],"5 Fluorouracil","5 Fluorouracilum","5 FU","5-Fluoro-2,4(1H, 3H)-pyrimidinedione","5-Fluorouracil","5-Fluracil","5-Fu","5FU","AccuSite","Carac","Fluoro Uracil","Fluouracil","Flurablastin","Fluracedyl","Fluracil","Fluril","Fluroblastin","Ribofluor","Ro 2-9757","Ro-2-9757",{"type":95,"name":96,"description":97,"armGroupLabels":98,"otherNames":99},"DEVICE","Holter Monitoring","Undergo Holter monitoring",[9,21,26,31],[100,101,102],"HOLTER CONTINUOUS ECG RECORDING","Holter Electrocardiography","Holter Monitor",{"type":47,"name":104,"description":56,"armGroupLabels":105,"otherNames":106},"Isosorbide Mononitrate",[21],[107,108,109,110],"Imdur","ISMO","Monoket","Monosordil",{"type":6,"name":112,"description":113,"armGroupLabels":114,"otherNames":115},"Medical Device Usage and Evaluation","Use EndoPAT",[9,21,26,31],null,{"type":47,"name":117,"description":56,"armGroupLabels":118,"otherNames":115},"Placebo Administration",[31],{"type":6,"name":120,"description":121,"armGroupLabels":122,"otherNames":115},"Questionnaire Administration","Ancillary studies",[9,21,26,31],[124],{"name":125,"affiliation":126,"role":127},"Joerg Herrmann, MD","Mayo Clinic in Rochester","PRINCIPAL_INVESTIGATOR",[129,134],{"name":130,"role":131,"phone":132,"phoneExt":115,"email":133},"Clinical Trials Referral Office","CONTACT","855-776-0015","mayocliniccancerstudies@mayo.edu",{"name":135,"role":131,"phone":136,"phoneExt":115,"email":115},"Interventional & Ischemic Heart Disease Research Team","507-255-1724",[138],{"facility":126,"status":139,"city":140,"state":141,"zip":142,"country":143,"countryCode":144,"cosmosGeoPoint":145,"geoPoint":150,"contacts":151},"RECRUITING","Rochester","Minnesota","55905","United States","US",{"type":146,"coordinates":147},"Point",[148,149],-92.4699,44.02163,{"lat":149,"lon":148},[152,153,154],{"name":130,"role":131,"phone":132,"phoneExt":115,"email":133},{"name":135,"role":131,"phone":136,"phoneExt":115,"email":115},{"name":125,"role":127,"phone":115,"phoneExt":115,"email":115},{"type":156,"investigatorFullName":115,"investigatorTitle":115,"investigatorAffiliation":115,"oldNameTitle":115,"oldOrganization":115},"SPONSOR","100628070","phase-1-vasodilator-therapy-with-isosorbide-mononitrate-or-diltiazem-to-reduce-vasotoxicity-in-patients-with-gastrointestinal-cancer-receiving-fluoropyrimidine-therapy-100628070",false,"NCT07456852","Vasodilator Therapy With Isosorbide Mononitrate or Diltiazem to Reduce Vasotoxicity in Patients With Gastrointestinal Cancer Receiving Fluoropyrimidine Therapy","Vasotoxicity Surveillance Using EndoPAT: The VASA Pilot Study","Inclusion Criteria:\n\n* REGISTRATION: Age ≥ 18 years\n* REGISTRATION: Histologically or cytologically confirmed gastrointestinal malignancy (colon, rectal, gastric, esophageal, or other GI cancer) for which fluoropyrimidine therapy (5-FU or capecitabine) is indicated, either as single agent or in combination with other systemic therapy\n* REGISTRATION: Planned initiation of 5-FU (infusional) or oral capecitabine therapy, either as standard chemotherapy or as a radiosensitizer\n* REGISTRATION: Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, or 2\n* REGISTRATION: Ability to return to Mayo Clinic for baseline and follow-up EndoPAT testing, electrocardiogram (ECG), Holter monitoring, and blood draws\n* REGISTRATION: Provide written informed consent\n* REGISTRATION: Adequate baseline hemodynamic status: systolic blood pressure ≥ 120 mmHg and resting heart rate ≥ 70 beats\u002Fminute (to ensure safety for potential vasodilator therapy in Phase II)\n* RANDOMIZATION: Completed all phase I baseline and follow-up assessments, including EndoPAT, ECG, high-sensitivity cardiac troponin T (hs-TnT), and Holter monitoring\n* RANDOMIZATION: Demonstrated a ≥ 20% decline in reactive hyperemia index (RHI) from baseline at either phase I follow-up assessment as measured by EndoPAT\n* RANDOMIZATION: Adequate hemodynamic status prior to randomization: systolic blood pressure ≥ 120 mmHg and resting heart rate ≥ 70 beats\u002Fminute\n* RANDOMIZATION: Ability to tolerate and comply with study medication (isosorbide mononitrate, diltiazem, or placebo) per investigator assessment\n* RANDOMIZATION: Willingness to initiate study medication 5 days before and continue through the assigned fluoropyrimidine treatment cycle\n* RANDOMIZATION: Provide written informed consent for randomization phase\n\nExclusion Criteria:\n\n* REGISTRATION: Current or planned treatment with long-acting nitrates or calcium channel blockers at the time of fluoropyrimidine initiation\n* REGISTRATION: Known hypersensitivity or contraindication to nitrates or calcium channel blockers\n* REGISTRATION: Baseline systolic blood pressure \\\u003C 120 mmHg or resting heart rate \\\u003C 70 beats\u002Fminute\n* REGISTRATION: History of myocardial infarction ≤ 6 months prior to registration, or symptomatic heart failure \\[decompensated or New York Heart Association (NYHA) III-IV\\] requiring ongoing therapy\n* REGISTRATION: Recent acute coronary syndrome or coronary revascularization within 3 months of enrollment\n* REGISTRATION: High-grade atrioventricular (AV) block without pacemaker\n* REGISTRATION: Use of PDE-5 inhibitors \\[e.g. sildenafil (Viagra)\\] within 48 hours of enrollment\n* REGISTRATION: Uncontrolled intercurrent illness including but not limited to: unstable angina, symptomatic arrhythmias, uncontrolled infection, or psychiatric\u002Fsocial conditions limiting compliance with study requirements\n* REGISTRATION: Physical inability to undergo EndoPAT testing (e.g., digital amputation, severe hand deformity, or other limiting condition)\n* REGISTRATION: Pregnant or nursing persons\n* REGISTRATION: Concurrent enrollment in another interventional clinical trial that, in the opinion of the investigator, would interfere with study endpoints","ALL","18 Years",{"count":167,"type":168},60,"ESTIMATED","INTERVENTIONAL",[171,172],"PHASE1","PHASE2","This phase I\u002FII trial compares the effect of drugs that causes widening of blood vessels as a result of smooth muscle relaxation (vasodilator therapy) with isosorbide mononitrate, diltiazem or placebo to reduce vasotoxicity in patients with gastrointestinal cancer receiving fluoropyrimidine therapy. Some patients develop chest pain (possibly even a heart attack, a drop in heart function, or a rhythm abnormality) during treatment with a class of cancer drugs known as fluoropyrimidines, which include 5-Fluorouracil (5-FU) and capecitabine. These side effects are believed to be due to the development of an abnormal reactivity of the blood vessels referred to as vasospasm. Vasotoxicity is damage or toxicity inflicted upon blood vessels (vascular system), often causing dysfunction, remodeling, or narrowing (vasoconstriction). It is a broad term used to describe the detrimental effects of certain agents, such as chemotherapy drugs. Researchers want to evaluate how often the reactivity of blood vessels becomes abnormal, during the treatment with 5-FU or capecitabine and how clinically relevant and controllable\u002Fpreventable this phenomenon is in patients with gastrointestinal cancer.",[175],"Malignant Digestive System Neoplasm","2026-05-29",{"date":178,"type":179},"2026-06-02","ACTUAL",{"date":181,"type":179},"2026-04-30",{"date":183,"type":168},"2030-04-30",{"name":5,"class":6},1]