[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100657431":3},{"organization":4,"outcomesModule":7,"designInfo":100,"detailedDescription":112,"studyPopulation":103,"armGroups":113,"interventions":126,"overallOfficials":135,"centralContacts":139,"locations":148,"responsibleParty":176,"collaborators":178,"id":181,"slug":182,"hasResults":183,"nctId":184,"briefTitle":185,"officialTitle":186,"acronym":187,"eligibilityCriteria":188,"healthyVolunteers":183,"sex":189,"minAge":190,"maxAge":191,"enrollmentInfo":192,"targetDuration":103,"studyType":195,"phases":196,"briefSummary":198,"conditions":199,"keywords":203,"overallStatus":150,"whyStopped":103,"lastUpdateSubmitDate":208,"lastUpdatePostDateStruct":209,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":217},{"fullName":5,"class":6},"Tan Tock Seng Hospital","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":89},[9],{"measure":10,"description":11,"timeFrame":12},"Change from Baseline in Mean-Maximum Carotid Intima-Media Thickness (Mean-Maximum CIMT)","Mean-maximum CIMT is defined as the average of the maximum CIMT values obtained from the far wall of the left and right common carotid arteries, each derived from six measurements taken across three projections (lateral, anterior, and posterior) at 1 cm proximal to the carotid bifurcation, measured by high-resolution B-mode carotid ultrasonography.","Baseline and 24 weeks",[14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71,74,77,80,83,86],{"measure":15,"description":16,"timeFrame":12},"Change from Baseline in Mean Carotid Intima-Media Thickness (avgCIMT)","Mean CIMT (avgCIMT) is defined as the average of all twelve individual IMT measurements obtained from the far wall of the left and right common carotid arteries (six measurements per side), measured by high-resolution B-mode carotid ultrasonography.",{"measure":18,"description":19,"timeFrame":12},"Change from Baseline in Carotid Plaque Volume","Carotid plaque volume is measured using 3D plaque volume software following standard acquisition protocol in participants with identified carotid plaque on ultrasonography.",{"measure":21,"description":22,"timeFrame":12},"Change from Baseline in Endothelial Function (Flow-Mediated Dilation)","Endothelial function is assessed by flow-mediated dilation (FMD) of the brachial artery using high-resolution ultrasound, expressed as the percentage change in brachial artery diameter following reactive hyperaemia.",{"measure":24,"description":25,"timeFrame":12},"Change from Baseline in Microvascular Reactivity (Reactive Hyperaemia Index)","Microvascular reactivity is assessed by the reactive hyperaemia index (RHI) measured using EndoPAT, a non-invasive device that quantifies peripheral arterial tone response to forearm occlusion.",{"measure":27,"description":28,"timeFrame":12},"Change from Baseline in Arterial Stiffness (Pulse Wave Velocity)","Arterial stiffness is assessed by carotid-femoral pulse wave velocity (PWV) measured using SphygmoCor XCEL, a validated applanation tonometry-based device.",{"measure":30,"description":31,"timeFrame":12},"Change from Baseline in Arterial Stiffness (Cardio-Ankle Vascular Index)","Arterial stiffness is additionally assessed by the cardio-ankle vascular index (CAVI), a measure of arterial stiffness from the origin of the aorta to the ankle that is less dependent on blood pressure at the time of measurement.",{"measure":33,"description":34,"timeFrame":12},"Change from Baseline in Skin Advanced Glycation End Products (Skin Autofluorescence)","Tissue advanced glycation end product (AGE) accumulation is measured non-invasively using the AGE Reader, which quantifies skin autofluorescence using ultraviolet light excitation.",{"measure":36,"description":37,"timeFrame":12},"Change from Baseline in Retinal Layer Thickness (Optical Coherence Tomography)","Retinal layer thickness is measured by optical coherence tomography (OCT) as a surrogate of retinal and systemic microvascular health.",{"measure":39,"description":40,"timeFrame":12},"Change from Baseline in Retinal Microvascular Density (Optical Coherence Tomography Angiography)","Retinal microvascular density is measured by optical coherence tomography angiography (OCTA) as a surrogate of systemic microvascular health.",{"measure":42,"description":43,"timeFrame":12},"Change from Baseline in High-Sensitivity C-Reactive Protein (hsCRP)","Serum high-sensitivity C-reactive protein (hsCRP) is measured as a marker of systemic inflammation.",{"measure":45,"description":46,"timeFrame":12},"Change from Baseline in Interleukin-6 (IL-6)","Plasma interleukin-6 (IL-6) is measured as a marker of systemic inflammation and cytokine activity.",{"measure":48,"description":49,"timeFrame":12},"Change from Baseline in Plasminogen Activator Inhibitor-1 (PAI-1)","Plasma plasminogen activator inhibitor-1 (PAI-1) is measured as a marker of impaired fibrinolysis and endothelial dysfunction.",{"measure":51,"description":52,"timeFrame":12},"Change from Baseline in Cell-Free DNA (NETosis Marker)","Plasma cell-free DNA is measured as a marker of neutrophil extracellular trap (NET) formation and neutrophil-mediated inflammatory activity.",{"measure":54,"description":55,"timeFrame":12},"Change from Baseline in Citrullinated Histone H3 (NETosis Marker)","Plasma citrullinated histone H3 is measured as a specific marker of neutrophil extracellular trap (NET) formation and NETosis.",{"measure":57,"description":58,"timeFrame":12},"Change from Baseline in E-selectin","Plasma E-selectin is measured as a marker of endothelial activation and inflammation.",{"measure":60,"description":61,"timeFrame":12},"Change from Baseline in Intercellular Adhesion Molecule-1 (ICAM-1)","Plasma ICAM-1 is measured as a marker of endothelial activation and leucocyte adhesion.",{"measure":63,"description":64,"timeFrame":12},"Change from Baseline in Vascular Cell Adhesion Molecule-1 (VCAM-1)","Plasma VCAM-1 is measured as a marker of endothelial activation and vascular inflammation.",{"measure":66,"description":67,"timeFrame":12},"Change from Baseline in Oxidative Stress Index","An integrated oxidative stress index is derived from nuclear magnetic resonance (NMR)-based redox profiling of plasma and erythrocytes, providing a composite measure of systemic oxidative stress.",{"measure":69,"description":70,"timeFrame":12},"Change from Baseline in Thrombotic Potential (Clot Waveform Analysis)","Clot waveform analysis is performed to characterise the kinetics of clot formation and fibrinolysis in plasma as a measure of overall thrombotic potential.",{"measure":72,"description":73,"timeFrame":12},"Change from Baseline in Von Willebrand Factor Antigen (VWF:Ag)","Plasma von Willebrand factor antigen (VWF:Ag) is measured as a marker of endothelial activation and thrombotic risk.",{"measure":75,"description":76,"timeFrame":12},"Change from Baseline in Von Willebrand Factor Activity (VWF:Act)","Plasma von Willebrand factor activity (VWF:Act) is measured as a functional marker of thrombotic risk and platelet adhesion capacity.",{"measure":78,"description":79,"timeFrame":12},"Change from Baseline in Factor VIII","Plasma factor VIII levels are measured as a marker of coagulation activation and thrombotic potential.",{"measure":81,"description":82,"timeFrame":12},"Change from Baseline in Thrombin Generation","Thrombin generation is measured using a calibrated automated thrombogram to assess overall coagulation potential and thrombotic risk.",{"measure":84,"description":85,"timeFrame":12},"Change from Baseline in Oxidised LDL (Ox-LDL)","Plasma oxidised LDL (Ox-LDL) is measured by nuclear magnetic resonance (NMR) spectroscopy as a marker of lipid oxidation and atherogenic risk.",{"measure":87,"description":88,"timeFrame":12},"Change from Baseline in Atherogenic Lipid Subfractions","Atherogenic lipid subfractions are characterised by nuclear magnetic resonance (NMR) spectroscopy, providing detailed lipoprotein particle profiling beyond standard lipid panels.",[90,93,96],{"measure":91,"description":92,"timeFrame":12},"Change from Baseline in Gut Microbiome Composition","Gut microbiome composition is characterised from stool samples by metagenomic sequencing, to examine whether colchicine-associated shifts in microbial composition relate to treatment response.",{"measure":94,"description":95,"timeFrame":12},"Change from Baseline in Plasma Metabolite Profile (Metabolomics)","As an exploratory analysis, plasma metabolomic profiling will be performed on stored blood samples to characterise changes in the metabolite profile over 24 weeks.",{"measure":97,"description":98,"timeFrame":99},"Incidence of Adverse Events and Serious Adverse Events","Safety is assessed by the incidence of adverse events (AEs) and serious adverse events (SAEs), defined per standard regulatory criteria, ascertained at each study visit and telephone contact, and adjudicated by an independent Data and Safety Monitoring Committee.","From randomisation through 24 weeks",{"allocation":101,"interventionModel":102,"interventionModelDescription":103,"primaryPurpose":104,"observationalModel":103,"timePerspective":103,"maskingInfo":105},"RANDOMIZED","PARALLEL",null,"PREVENTION",{"masking":106,"maskingDescription":103,"whoMasked":107},"QUADRUPLE",[108,109,110,111],"PARTICIPANT","CARE_PROVIDER","INVESTIGATOR","OUTCOMES_ASSESSOR","Cardiovascular disease remains the leading cause of death in T2DM, occurring earlier and at substantially higher rates than in the general population. Despite optimisation of conventional risk factors, residual cardiovascular risk remains high, with chronic low-grade inflammation driven by dysregulated neutrophil activity recognised as a key contributor. Patients with T2DM exhibit a distinct pro-inflammatory neutrophil phenotype characterised by increased neutrophil extracellular trap (NET) formation, heightened endothelial adherence, and altered rolling kinetics, which correlates with impaired vascular function and subclinical atherosclerosis.\n\nColchicine inhibits neutrophil activation, migration, and NET formation, and has demonstrated efficacy in secondary cardiovascular prevention in large randomised trials. Evidence in primary prevention, particularly in T2DM, remains limited. Col-DM takes a precision medicine approach, hypothesising that colchicine's benefit will be concentrated among T2DM patients with a high-risk inflamed neutrophil signature rather than being uniform across the broader population.\n\nCol-DM is a 24-week, parallel-group, Phase 2 randomised controlled trial. Adults with T2DM and no prior atherosclerotic cardiovascular disease are randomised 1:1 to colchicine 0.5 mg daily or matched placebo, stratified by neutrophil inflammatory phenotype classified using a microfluidic organ-on-chip platform. The primary outcome is progression of carotid intima-media thickness (CIMT), estimated overall and separately within each neutrophil-signature stratum. Secondary outcomes cover vascular function, inflammatory and oxidative stress biomarkers, and thrombotic potential. Gut microbiome composition is examined as an exploratory outcome. All outcome measures are estimated overall and separately within each neutrophil-signature stratum. Safety is monitored by an independent Data and Safety Monitoring Committee.",[114,120],{"label":115,"type":116,"description":117,"interventionNames":118},"Colchicine","EXPERIMENTAL","Colchicine 0.5 mg orally once daily for 24 weeks, in addition to usual risk-factor-based therapy",[119],"Drug: Colchicine 0.5 MG Oral Tablet Once Daily",{"label":121,"type":122,"description":123,"interventionNames":124},"Placebo","PLACEBO_COMPARATOR","Matched placebo orally once daily for 24 weeks, in addition to usual risk-factor-based therapy",[125],"Drug: Placebo",[127,132],{"type":128,"name":129,"description":130,"armGroupLabels":131,"otherNames":103},"DRUG","Colchicine 0.5 MG Oral Tablet Once Daily","For 24 weeks",[115],{"type":128,"name":121,"description":133,"armGroupLabels":134,"otherNames":103},"Matched placebo tablets (identical in size, shape, taste, and packaging to colchicine), once daily, for 24 weeks",[121],[136],{"name":137,"affiliation":5,"role":138},"Rinkoo Dalan, MD, PhD","PRINCIPAL_INVESTIGATOR",[140,145],{"name":141,"role":142,"phone":143,"phoneExt":103,"email":144},"Sanchalika Acharyya, PhD, MPH","CONTACT","96150202","sanchalika.acharyya@nhghealth.com.sg",{"name":146,"role":142,"phone":103,"phoneExt":103,"email":147},"Shirley Lin Shangmei","ttsh.p2p.research@nhghealth.com.sg",[149],{"facility":5,"status":150,"city":151,"state":151,"zip":152,"country":151,"countryCode":153,"cosmosGeoPoint":154,"geoPoint":159,"contacts":160},"RECRUITING","Singapore","308433","SG",{"type":155,"coordinates":156},"Point",[157,158],103.85007,1.28967,{"lat":158,"lon":157},[161,164,165,168,170,172,174],{"name":137,"role":142,"phone":162,"phoneExt":103,"email":163},"65-6357100","rinkoo.dalan@nhghealth.com.sg",{"name":137,"role":138,"phone":103,"phoneExt":103,"email":103},{"name":166,"role":167,"phone":103,"phoneExt":103,"email":103},"Ying Jie Chee, MD","SUB_INVESTIGATOR",{"name":169,"role":167,"phone":103,"phoneExt":103,"email":103},"Rupesh Agrawal, M Med (Ophth), MD (Research)",{"name":171,"role":167,"phone":103,"phoneExt":103,"email":103},"Huiling Liew, MD",{"name":173,"role":167,"phone":103,"phoneExt":103,"email":103},"Ying Shan Lee, MBBS",{"name":175,"role":167,"phone":103,"phoneExt":103,"email":103},"Eugene Fan, MD",{"type":177,"investigatorFullName":103,"investigatorTitle":103,"investigatorAffiliation":103,"oldNameTitle":103,"oldOrganization":103},"SPONSOR",[179],{"name":180,"class":6},"Nanyang Technological University","100657431","phase-2-colchicine-for-primary-prevention-of-cardiovascular-disease-in-adults-with-type-2-diabetes-100657431",false,"NCT07837934","Colchicine for Primary Prevention of Cardiovascular Disease in Adults With Type 2 Diabetes","The Role of Colchicine in Preventing Atherosclerotic Cardiovascular Disease in Type 2 Diabetes (Col-DM Study)","Col-DM","Inclusion Criteria:\n\n* T2DM on stable diabetes medications (no change in last 3 months)\n* At least one other comorbidity of hypertension, dyslipidaemia and\u002For obesity (BMI ≥27), with no previous history of ASCVD\n* Able to provide informed consent\n\nExclusion Criteria:\n\n1. Recent hospitalization or acute infections within last 2 weeks.\n2. Current Treatment with corticosteroids or immunosuppressive agents\n3. Pre-existing malignancies or other terminal conditions with limited prognosis\n4. Pregnancy\n5. Breastfeeding\n6. Inability to provide written consent\n7. Renal impairment (eGFR\\\u003C 60ml\u002Fmin)\n8. Liver cirrhosis or ALT\u002FAST \\>3x ULN\n9. Pharmacogenomics indicative of adverse effects\n10. Hypersensitivity to the active substance or to the following excipients: Lactose, Maize starch, Sodium laurilsulfate, Magnesium stearate\n11. Known blood dyscrasia\n12. Women of childbearing age who are keen to conceive in the next 1 year\n13. Taking a strong P-glycoprotein inhibitor (e.g. cyclosporine, ranolazine) or a strong CYP3A4 inhibitor\n14. Known myositis with raised creatine kinase with statins (statin myopathy).\n15. Gout attack within the last 1 year\n16. Currently taking Aspirin\n17. Taking any oral contraceptives","ALL","21 Years","80 Years",{"count":193,"type":194},300,"ESTIMATED","INTERVENTIONAL",[197],"PHASE2","This study will test whether a low-cost anti-inflammatory medicine called colchicine can help protect the blood vessels of people with type 2 diabetes. Diabetes speeds up hardening of the arteries (atherosclerosis), partly because of ongoing low-grade inflammation. Colchicine has already been shown to help prevent heart attacks and strokes in people who already have heart disease; this study looks at whether it can also help prevent early blood vessel damage before heart disease develops. Around 300 adults with type 2 diabetes will be randomly assigned to take colchicine or a placebo (dummy pill) once daily for 24 weeks, in addition to their usual diabetes and heart-risk medications. Neither participants nor the study team will know who is taking colchicine or placebo. The main measurement will be the change in the thickness of the wall of the neck (carotid) artery, measured by ultrasound, which is an early sign of blood vessel disease. The study will also look at markers of inflammation in the blood, blood vessel stiffness and function, and changes in the gut bacteria.",[200,201,202],"Type 2 Diabetes Mellitus (T2DM)","Atherosclerosis","Cardiovascular Diseases",[115,204,205,206,207],"Inflammation","Neutrophils","Carotid Intima-Media Thickness","Primary Prevention","2026-09-20",{"date":210,"type":211},"2026-09-24","ACTUAL",{"date":213,"type":211},"2025-07-24",{"date":215,"type":194},"2027-07-31",{"name":5,"class":6},1]