[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sex-differences\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sex-differences":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,39,81,113,139,165,194,230],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100631569","sex-dependent-risk-of-postoperative-delirium-and-mediating-effects-of-family-visits-100631569",false,"NCT07502391","Sex-Dependent Risk of Postoperative Delirium and Mediating Effects of Family Visits","Sex-Dependent Risk of Postoperative Delirium and Mediating Effects of Family Visits: A Prospective Observational Study","Inclusion Criteria:\n\n* Informed consent as documented by signature;\n* ≥65 years of age;\n* Scheduled non-cardiac surgery with expected surgery duration ≥ 2 hours;\n* Under either general or spinal anesthesia.\n\nExclusion Criteria:\n\n* Known drug or alcohol abuse;\n* Requirement for postoperative ventilation;\n* Current participation in another study with an investigational drug;\n* Inability to complete the study assessments.","ALL","65 Years",{"count":19,"type":20},471,"ESTIMATED","OBSERVATIONAL","Postoperative delirium is a common and serious complication after surgery, affecting 10-40% of older patients undergoing non-cardiac procedures. It is characterized by sudden changes in attention, awareness, and thinking that fluctuate throughout the day. Delirium is associated with longer hospital stays, higher mortality, worse long-term brain function, and substantially increased healthcare costs. While several risk factors are known, it remains unclear whether a patient's sex independently influences the risk of developing postoperative delirium, as existing studies have produced conflicting results and were often not designed to specifically examine sex differences.Family visitation is a promising non-drug approach to preventing delirium. Studies in intensive care patients have shown that those who receive family visits have a significantly lower risk of developing delirium. However, it is unknown whether men and women receive different amounts of family visits after surgery, and whether any such difference could help explain sex-based disparities in delirium risk. Given that traditional gender roles in caregiving persist, women - who often serve as primary caregivers in their families - may receive fewer visits when they themselves become patients.This prospective observational study led by the University of Zurich will enroll 471 patients aged 65 years or older undergoing non-cardiac surgery lasting at least 2 hours under general or spinal anesthesia. The primary aim is to determine whether female patients have a higher risk of developing postoperative delirium within three days after surgery compared to male patients. Delirium will be assessed twice daily using the 4 A's Test (4AT), a validated and standardized screening tool. The secondary aim is to evaluate whether female patients receive fewer family visits than male patients and whether any difference in visitation mediates the sex-dependent delirium risk. Family visits will be recorded using an anonymous sign-in sheet placed in the patient's room. The study does not involve any experimental interventions; all patients receive standard clinical care. Participation is voluntary, and withdrawal is possible at any time without affecting medical treatment.",[24,25],"Postoperative Delirium (POD)","Sex Differences","RECRUITING","2026-05-27",{"date":29,"type":30},"2026-06-01","ACTUAL",{"date":32,"type":30},"2026-05-05",{"date":34,"type":20},"2028-12-31",{"name":36,"class":37},"Julian Rössler","OTHER",1,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":60,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":5},"100580704","phase-4-effects-of-donor-recipient-sex-matched-blood-transfusion-on-patient-outcomes-100580704","NCT06840756","Effects of Donor-recipient Sex-matched Blood Transfusion on Patient Outcomes","Effects of Donor-recipient Sex-matched Versus Sex-mismatched Red Blood Cell Transfusion on Outcomes in Critically Ill Adult Patients","SexMATTERS RCT","Inclusion Criteria:\n\n* Adults (age ≥18);\n* Admission to a participating ICU;\n* Requiring RBC transfusion.\n\nExclusion Criteria:\n\n* Requirement for a specialized RBC product or unit not readily available in inventory (e.g., rare blood type, washed RBCs, complex RBC antibodies, etc.);\n* Massively bleeding patient (i.e., ≥4 units of blood ordered at one time, or Massive Hemorrhage Protocol initiated, or an urgent blood request made);\n* Sex unknown or sex other than male or female (i.e. intersex);\n* Do not have a valid Ontario Health Insurance Plan (OHIP) health card number.","18 Years",{"count":49,"type":20},11082,"INTERVENTIONAL",[52],"PHASE4","Red blood cell (RBC) transfusions are selected based upon matching donor and recipient blood group: donor and recipient sex are not considered when selecting blood for transfusion. Hence, transfused patients can currently receive sex-matched and\u002For unmatched RBCs when transfusions are given. Sex-matched stem cell transplants, and some solid organ transplants, have shown that sex-matching donor to recipient improves patient outcomes. Recent exploratory studies have also suggested that patient outcomes could be improved by sex-matching for RBC transfusion. There is emerging evidence of underlying biologic mechanism(s) to support these observations. This study is designed as a randomized controlled trial and will explore the impact on patients who receive RBC transfusions from donors of the same sex (\"sex-matched\") compared with donors of the opposite sex (\"sex-mismatched\").\n\nThe trial will study adult patients admitted to the Intensive Care Unit who require an RBC transfusion. Patients will be assigned (through a process called randomization) to receive sex-matched RBCs or sex-mismatched RBCs to determine if there is a difference in mortality between those receiving matched versus mismatched RBCs. The results of this trial could have direct implications on resources, blood inventory, and RBC transfusion ordering practices.",[55,25,56,57,58,59],"Red Blood Cell Transfusions","Health Services","Critically Ill Intensive Care Unit Patients","Hematology","Cardiovascular",[61,62,63,64,65,66,67,68,69,70,71],"transfusions","red blood cell transfusions","sex-matched","sex-mismatched","intensive care unit","ICU","cardiovascular","circulatory","hematology","mortality","blood donor characteristics","2026-03-10",{"date":74,"type":30},"2026-03-12",{"date":76,"type":30},"2025-09-11",{"date":78,"type":20},"2029-03-31",{"name":80,"class":37},"Michelle Zeller",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":88,"sex":16,"minAge":47,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":50,"phases":92,"briefSummary":94,"conditions":95,"keywords":97,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":38},"100626871","does-circadian-misalignment-have-sex-specific-effects-on-metabolism-100626871","NCT07441265","Does Circadian Misalignment Have Sex-Specific Effects on Metabolism?","Role of Biological Sex in Metabolic Responses to Night Work","Inclusion Criteria:\n\n* 18-40 years of age\n* Body Mass Index 18.5-24.9 kg\u002Fm2\n* Non-smokers, no current tobacco or e-cigarette use\n* Healthy with no acute or chronic medical and psychiatric disorders\n* Sex assigned at birth consistent with reproductive anatomy at enrollment (per protocol definition)\n\nExclusion Criteria:\n\n* History of drug or alcohol dependency\n* History of psychiatric illness or disorder\n* Pregnant\n* No prior gender-affirming hormone therapy and no gonadectomy",true,"40 Years",{"count":91,"type":20},36,[93],"NA","This study will test whether biological sex influences how the body responds to circadian misalignment-a mismatch between the internal body clock and the timing of sleep and eating (as can occur with shift work or jet lag). Researchers will examine how circadian misalignment affects appetite regulation (hunger\u002Ffullness) and glucose metabolism (blood sugar control), and whether these effects differ between females and males. Findings may help inform more personalized shift work schedules and targeted strategies to reduce metabolic health risks and sex-related differences in clinical care.",[96,25],"Circadian Misalignment",[98,99,100,101,102],"circadian rhythm","sex differences","night work","glucose control","appetite regulation","NOT_YET_RECRUITING","2026-02-23",{"date":106,"type":30},"2026-02-27",{"date":108,"type":20},"2026-10-01",{"date":110,"type":20},"2030-09-30",{"name":112,"class":37},"Brigham and Women's Hospital",{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":88,"sex":16,"minAge":119,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":50,"phases":123,"briefSummary":124,"conditions":125,"keywords":4,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":38},"100609294","the-role-of-estrogen-and-testosterone-in-determining-brain-blood-flow-and-metabolic-regulation-in-humans-100609294","NCT07212712","The Role of Estrogen and Testosterone in Determining Brain Blood Flow and Metabolic Regulation in Humans","Inclusion Criteria:\n\nThe investigators will recruit healthy young (18-40 years) males (n = 25) and females (n = 25). Females must be naturally cycling (i.e., no oral or hormonal contraceptives), not pregnant, and premenopausal. Participants must be normotensive (\\\u003C140\u002F90 mmHg \\& \\>90\u002F60 mmHg) and have no medical history of cerebrovascular, cardiopulmonary, cardiovascular, neuromuscular, and renal disease assessed by a study questionnaire. A recent physical examination (within 1 year of participation) from a family physician or a completed physical examination by the study doctor is required prior to participation. All subjects will sign an informed consent form prior to participation.\n\nParticipants will be excluded if they meet any of the following criteria:\n\n* Hypertensive (≥140\u002F90 mmHg) or hypotensive (≤90\u002F60 mmHg)\n* BMI ≥ 30 kg\u002Fm2\n* Fasting blood glucose ≥ 100 mg\u002FdL\n* Abnormal results on standard blood hematology tests (e.g., complete blood count, comprehensive metabolic panel)\n* Males with hypogonadism (total testosterone ≤ 262 ng\u002FdL, per Endocrine Society recommendations)\n* Any history of cerebrovascular, cardiopulmonary, cardiovascular, neuromuscular, or renal disease\n* Any liver dysfunction or disease\n* Taking any cardiovascular medications or medications that would interfere with study medications (e.g., strong organic anion transporting polypeptide 1B1 inhibitors)\n* Contraindications or sensitivities to study medications\n* Current eating disorder (defined as \\>2 on the 'SCOFF' questionnaire 67)\n* Current smokers\n* Females with an irregular menstrual cycle or any medical conditions affecting the menstrual cycle (normal cycle defined as 21-35 days from menstrual cycle diary)\n* Females who are pregnant (assessed with pregnancy test at screening and prior to starting medications), breastfeeding, or planning to conceive within 3 months\n* Females using hormonal birth control (Copper intrauterine devices \\[IUDs\\] will be allowed as they do not change systemic hormone levels)\n* Females who are peri- or postmenopausal (as determined by STRAW criteria 68)\n* History of hormone-sensitive cancers (i.e., breast, ovarian, uterine or prostate)\n* Z-score \\\u003C -2 as assessed with DXA scan (to determine risk of decrease in bone mineral density)\n* Assessed using the Center for Epidemiologic Studies Depression (CES-D) scale, participants with a score \\> 16 at screening unless otherwise approved by the study MD","18 Weeks","40 Weeks",{"count":122,"type":20},50,[93],"Due to historical exclusion of females from research, there are gaps in the understanding of female physiology, how it differs from males, and how sex-specific hormones contribute. As a result, many diagnoses and treatments are based on male physiology and may not be appropriate or effective for females. Females consistently experience greater risk and report worse neurological outcomes in many diseases, including stroke, cardiac arrest, and dementia. As research in females progresses, differences between sexes and changes throughout the lifespan (e.g., puberty, menopause) highlight the importance of understanding the effects of sex and sex-specific hormones on the body. The brain is arguably the most important organ in the body, consuming 20% of the body's total energy. Previous research supports higher blood flow to the brain in females, and research in animals suggests hormones such as estrogen, progesterone, and testosterone are responsible. However, it is extremely difficult to isolate these hormones in humans, due to natural fluctuations (i.e., menstrual cycle). Therefore, the investigators plan to explore the direct role of these sex-specific hormones in regulating blood flow to the brain by blocking hormone production in healthy males and females and giving back testosterone and estrogen, respectively. The investigators will then conduct a range of tests to look at blood flow to the brain at rest and during various stressors. This research will provide crucial insight into how males and females differ in regulation of brain blood flow and inform new treatments and therapies to a wide range of brain injuries and diseases, improving outcomes and reducing the sex disparity in clinical pathways.",[126,127,25,128,129],"Cerebral Blood Flow","Cerebral Blood Flow Regulation","Exercise","Vascular","2026-02-06",{"date":132,"type":30},"2026-02-10",{"date":134,"type":20},"2026-04-01",{"date":136,"type":20},"2027-12-31",{"name":138,"class":37},"University of British Columbia",{"id":140,"slug":141,"hasResults":11,"nctId":142,"briefTitle":143,"officialTitle":143,"acronym":4,"eligibilityCriteria":144,"healthyVolunteers":88,"sex":16,"minAge":145,"maxAge":89,"enrollmentInfo":146,"targetDuration":4,"studyType":50,"phases":148,"briefSummary":149,"conditions":150,"keywords":153,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":38},"100578263","evaluation-of-sex-differences-in-glucose-metabolism-in-response-to-sleep-curtailment-100578263","NCT06809023","Evaluation of Sex Differences in Glucose Metabolism in Response to Sleep Curtailment","Inclusion Criteria:\n\n* Healthy adults with conventional sleep-wake timing\n* Non-smokers\n* Completion of medical, psychological, and sleep screening tests\n* Able to spend 5 consecutive days\u002Fnights in the laboratory on two separate occasions (total of 10 days\u002Fnights in the laboratory)\n* Women must have a recent history of regular menstrual cycles\n\nExclusion Criteria:\n\n* History of neurological or psychiatric disorder\n* History of sleep disorder or regular use of sleep-promoting medication\n* Current prescription, herbal, or over-the-counter medication use including hormonal birth control\n* Traveling across 2 or more time zones within past 3 months\n* Donating blood within past 8 weeks\n* Worked night or rotating shift work within past year\n* Hearing impairment, visual impairment\n* History of eye trauma or surgery\n* Drug or alcohol dependency","20 Years",{"count":147,"type":20},32,[93],"The goal of this study is to learn whether insufficient sleep affects glucose metabolism differently in healthy men and women.",[151,25,152],"Sleep Deprivation","Glucose Tolerance",[154,155,99,156],"glucose metabolism","sleep deprivation","GLP-1","2025-12-09",{"date":159,"type":30},"2025-12-10",{"date":161,"type":20},"2026-04",{"date":163,"type":20},"2029-02",{"name":112,"class":37},{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":4,"eligibilityCriteria":171,"healthyVolunteers":88,"sex":16,"minAge":47,"maxAge":172,"enrollmentInfo":173,"targetDuration":4,"studyType":50,"phases":175,"briefSummary":176,"conditions":177,"keywords":4,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":4},"100612630","effects-of-transcutaneous-auricular-vagus-nerve-stimulation-on-cognitive-performance-and-sex-differences-100612630","NCT07256080","Effects of Transcutaneous Auricular Vagus Nerve Stimulation on Cognitive Performance and Sex Differences","A Sham-Controlled Cross-Over Study Examining the Effects of Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) on Cognitive Performance and Gender Differences in Healthy Adults","Inclusion Criteria:\n\n* Healthy young adults aged 18-30 years\n* Ability to provide informed consent\n* Right-handed participants (to reduce variability in cognitive performance)\n* Normal or corrected-to-normal vision and hearing\n* Female participants tested during the follicular phase of the menstrual cycle (days 5-10) to minimize hormonal effects on cognition and vagal tone\n\nExclusion Criteria:\n\n* History of neurological or psychiatric disorders\n* Cardiovascular disease\n* Use of psychoactive medications\n* Substance dependence, including alcohol, illicit drugs, or nicotine\n* Pregnancy or breastfeeding\n* Skin conditions or ear anomalies that interfere with electrode placement\n* Metal implants in the head or neck region\n* History of epilepsy or migraine","30 Years",{"count":174,"type":20},60,[93],"This study investigates the effects of transcutaneous auricular vagus nerve stimulation (taVNS) on cognitive performance in healthy adults. The study uses a sham-controlled, cross-over design in which each participant receives both active taVNS and sham stimulation in separate sessions. Each participant completes both conditions (active and sham) in a randomized order using a crossover design. Cognitive performance will be assessed before and after each session using standardized tests. The study also explores whether males and females respond differently to taVNS, in order to identify potential sex-related differences in cognitive outcomes.",[178,179,180,181,182,183,184,25],"Cognitive Assessment","Cognition","taVNS","Vagus Nerve Stimulation","Executive Functions","Healthy Participants","Neuromodulation","2025-11-27",{"date":187,"type":30},"2025-12-01",{"date":189,"type":20},"2025-12",{"date":191,"type":20},"2026-05",{"name":193,"class":37},"Bahçeşehir University",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":200,"eligibilityCriteria":201,"healthyVolunteers":88,"sex":16,"minAge":202,"maxAge":203,"enrollmentInfo":204,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":206,"conditions":207,"keywords":215,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":222,"lastUpdatePostDateStruct":223,"startDateStruct":225,"completionDateStruct":226,"leadSponsor":228,"locationsCount":38},"100573300","oral-breath-test-to-measure-anabolic-sensitivity-to-a-protein-meal-across-the-age-and-physical-activity-spectrum-100573300","NCT06744491","Oral 'Breath Test' to Measure Anabolic Sensitivity to a Protein Meal Across the Age and Physical Activity Spectrum","Anabolic Sensitivity Across the Lifespan","NFRF","Inclusion Criteria:\n\n* Healthy will be defined as screened by the PAR-Q+ (The Physical Activity Readiness Questionnaire for everyone)\n* Chronological age for Healthy Young (age: 18-35 years) or Older (age: 60-80 years) adults\n* Chronological age between 8 to 16 years, with maturity offset \\\u003C -1 year from age of Peak Height Velocity (aPHV) for children and between -0.5 to +1.5 years from aPHV in adolescent participants\n* BMI between normal to overweight (18.5 - 29.9 kg\u002Fm2)\n\nExclusion Criteria:\n\n* Regular use of nonsteroidal anti-inflammatory dugs (with the exception of daily low-dose aspirin)\n* use of anticoagulants\n* use of a walker, cane, or assistive walking device\n* infectious or gastrointestinal disease\n* inability to comply with study protocol (e.g., unable to track diet)\n* regular tobacco use\n* self-reported illicit drug use (e.g., growth hormone, testosterone, etc.)\n* diagnosed chronic illness (e.g., type 2 diabetes, heart disease, thyroid disease)\n* pregnant\n* hormonal replacement therapy","8 Years","80 Years",{"count":205,"type":20},80,"The purpose of this study is to determine how anabolic sensitivity, in response to the ingestion of a liquid protein meal, differs across the lifespan, between biological sexes, and with varying physical activity levels.",[208,209,210,211,25,212,213,214],"Inactivity, Physical","Aging","Healthy Aging","Growth & Development","Anabolic Sensitivity","Protein Metabolism","Physical Activity",[216,217,218,219,220,221],"anabolic sensitivity","aging","growth and development","physical activity","skeletal muscle","stable isotopes","2024-12-16",{"date":224,"type":30},"2024-12-20",{"date":224,"type":20},{"date":227,"type":20},"2025-08-31",{"name":229,"class":37},"University of Toronto",{"id":231,"slug":232,"hasResults":11,"nctId":233,"briefTitle":234,"officialTitle":235,"acronym":236,"eligibilityCriteria":237,"healthyVolunteers":88,"sex":16,"minAge":238,"maxAge":239,"enrollmentInfo":240,"targetDuration":4,"studyType":50,"phases":242,"briefSummary":243,"conditions":244,"keywords":4,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":247,"lastUpdatePostDateStruct":248,"startDateStruct":250,"completionDateStruct":252,"leadSponsor":253,"locationsCount":4},"100409415","the-effect-of-team-sports-on-the-risk-of-thrombosis-in-elderly-individuals-in-a-municipality-setting-team-age-100409415","NCT04611191","The Effect of Team Sports on the Risk of Thrombosis in Elderly Individuals in a Municipality Setting (TEAM-AGE)","The Effect of Team Sports on the Susceptibility to Thrombosis in Elderly Men and Women in a Municipality Setting","TEAM-AGE","Inclusion Criteria:\n\n* Age: 60-70 years\n* Physical activity ≤ 2 hours per week (except transportation by bike or by walking)\n* BMI ≤ 30\n\nExclusion Criteria:\n\n* Age \\\u003C60 years\n* Injuries that prevent the performance of team sports\n* Participation in other clinical projects\n* Smokes or has smoked within the last 10 years\n* On hormone therapy (women)\n* Not entered menopause (women)\n* Has chronic diseases that are not expected, cf. the groups sought. Including heart problems, atrial fibrillation, cancer, immune diseases and previous strokes with functionally significant sequelae\n* Being treated with oral steroids\n* Has alcohol \u002F drug abuse or is being treated with disulfiram (Antabus)\n* Is unable to understand the contents of the document with informed consent or the experimental procedures","60 Years","70 Years",{"count":241,"type":20},400,[93],"Cardiovascular disease, and especially myocardial infarction, is the most common cause of death globally, and is particularly common in older individuals. Practical measures that can reduce both the prevalence and incidence of cardiovascular disease are of great value. It is well known that regular physical activity has a protective effect against the development of cardiovascular diseases such as acute myocardial infarction. It has been shown that physical activity can improve the function of the heart and blood vessels, but it is less well known how physical activity can affect the risk of formation of dangerous blood clots, and thus the risk of heart attack and stroke.\n\nIn a cross-sectional study it has been shown that a physically active lifestyle can reduce the risk of blood clot formation, but experimental evidence for the importance of a period of physical activity for the risk of blood clot formation is lacking. New methods have been set up for measuring the coagulation profile. The analyzes are performed on a blood sample and allow a thorough determination of platelet reactivity as well as an innovative measure of how the microstructure of a possible blood clot would develop. In this project, these methods is used to examine how physical activity, in the form of team sports, affects the coagulation profile of elderly men and women.\n\nThe increasing age-related risk of cardiovascular disease is associated with endothelial dysfunction and decrease in capillary density, and it has been shown that initiation of capillary growth is a successful method to treat cardiovascular disease. Therefore, this project will also investigate how a longer period of physical activity, in the form of team sports, affects capillary density and endothelial function in men and women aged 60-70 years. Both men and women will be recruited, as it is still unknown whether men and women respond differently to physical activity in relation to coagulation profile, susceptibility to blood clots and capillary density.",[245,246,25],"Thrombosis","Exercise Training","2023-05-09",{"date":249,"type":30},"2023-05-11",{"date":251,"type":20},"2024-12-30",{"date":136,"type":20},{"name":254,"class":37},"University of Copenhagen"]