[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sengkang General Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":241},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,43,70,103,131,161,187,211],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100570553","phase-3-regime-for-vitamin-d-maintenance-in-post-operative-patients-100570553",false,"NCT06708741","Regime for Vitamin D Maintenance in Post-Operative Patients","Regime for Vitamin D Maintenance in Post-Operative Patients (D-ECISIVE) Randomized Controlled Trial","D-ECISIVE","Inclusion Criteria:\n\n* Serum 25-hydroxyvitamin D levels between 30-50ng\u002Fml at 4-6 weeks after operation\n* aged 21-65 years\n* ability to provide informed consent\n* accepts to take vitamin D supplements post-operatively and\n* have their serum vitamin D levels checked periodically.\n\nExclusion Criteria:\n\n* They have undergone minor procedures (Table code \\\u003C4a)\n* have a history of chronic kidney disease\u002Fend staged renal failure\n* have previous history of ureteric\u002Fkidney stones\n* known hyperparathyroidism\n* are non-ambulatory independently\n* have had known allergies to the commercially available high dose vitamin D formulations.\n* Vulnerable personnel would be excluded from the study",true,"ALL","21 Years","65 Years",{"count":22,"type":23},100,"ESTIMATED","INTERVENTIONAL",[26],"PHASE3","Vitamin D plays a significant part calcium and phosphate haemostasis, thus, intrinsically critical for bone health. Increasing evidence also reveal that insufficient serum vitamin D levels also result in poor muscle health with such individuals having a compromised muscle building potential (4 times slower muscle building).\n\nMuscle health is a critical component of a post-surgical patient recovery, with impaired muscle function leading to reduced functional ability, resulting in a poorer quality of life. Poor muscle health also has negative repercussion on survivability, with reduced overall, and disease-specific survival, especially shown in cancer patients. Thus, maintenance of vitamin D levels post-surgery may be more critical than previously thought.",[29],"Sarcopenia","RECRUITING","2026-04-28",{"date":33,"type":34},"2026-05-04","ACTUAL",{"date":36,"type":34},"2026-01-01",{"date":38,"type":23},"2027-06-30",{"name":40,"class":41},"Sengkang General Hospital","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":51,"enrollmentInfo":52,"targetDuration":54,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":64,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":42},"100502487","review-of-the-impact-of-a-computer-aided-real-time-polyp-detection-system-on-adult-colonoscopy-100502487","NCT05822895","Review of the Impact of a Computer-aided Real-time Polyp Detection System on Adult Colonoscopy","A Comprehensive Review of the Impact of a COmPuter-aIded reaL-time pOlyp deTection System on Adult Colonoscopy (COPILOT Study) - a Single Institution Adoption Experience","COPILOT","Inclusion Criteria:\n\n* all adult patients going for colonoscopy in the our institution\n\nExclusion Criteria:\n\n* Patients with incomplete or failed colonoscopy, flexible sigmoidoscopy, colonoscopy done after previous colorectal cancers or previous colonic resections, patients with poor bowel preparation, when deemed by the endoscopist to have an incomplete assessment of the colon","90 Years",{"count":53,"type":23},764,"1 Month","OBSERVATIONAL","Background:\n\nRemoval of adenomatous polyps during colonoscopy is associated with long-term prevention of colorectal cancer-related deaths. Recently, there have been much interest in the use of artificial intelligence (AI) platforms to augment the routine endoscopic assessment of the colon to enhance adenoma detection rate (ADR). To date, computer assisted detection of polyps (CADe) have been shown to be safe, with a significant increase in ADR, without any concomitant increase in post-procedural complications.\n\nAims:\n\nThe investigators aim to evaluate the use of GI GeniusTM Intelligent Endoscopy Module in a multi-ethnic Asian population (Singapore) to increase in ADR and adenoma detected per colonoscopy (ADPC)to justify its effectiveness as an adjunct in polyp detection and training for colonoscopy.\n\nMethods:\n\nThis study will be a single-institution cohort study, conducted over a 2-year period. Sengkang General Hospital (SKH) does an estimated 12,500 colonoscopies per year, with an average of 1,040 colonoscopies performed every month. Thus, given the case volume, the investigators expect to detect differences in ADR amongst endoscopists if any during this study period.\n\nAs part of the subgroup analysis, the investigators also aim to compare the ADR rates of trainee endoscopists with and without the GI GeniusTM Intelligent Endoscopy Module to ascertain its utility as an education tool\u002Ftraining adjunct",[58],"Colonic Polyp",[60,61,62,63],"Colonic polyp","colonoscopy","artificial intelligence","implementation science",{"date":33,"type":34},{"date":66,"type":34},"2023-01-02",{"date":68,"type":23},"2031-12-31",{"name":40,"class":41},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":17,"sex":18,"minAge":77,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":24,"phases":80,"briefSummary":82,"conditions":83,"keywords":88,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":42},"100629660","optimizing-intrinsic-capacity-for-functional-independence-and-to-impede-frailty-in-older-adults-adaptation-of-the-who-icope-for-healthy-ageing-in-singapore-100629660","NCT07477561","Optimizing INtrinsic Capacity for Functional INdependence and to Impede FrailTY in Older Adults: Adaptation of the WHO-ICOPE for Healthy Ageing in Singapore","INFINITY-ICOPE","Inclusion Criteria: (in Phases 1, 2 and 3):\n\n* Any Singaporean or Permanent Resident (PR) aged 60 years and above\n* Able to provide informed consent (or legally acceptable representative available)\n\nExclusion Criteria (in Phases 1, 2 and 3):\n\n* Non-Singaporeans or non-PRs under 60 years of age\n* Residents of sheltered or nursing homes","60 Years",{"count":79,"type":23},600,[81],"NA","The goal of this intervention study is to screen and identify frailty and decline in intrinsic capacity (physical and mental capacities) in community-dwelling older adults in Singapore, and to evaluate whether early identification and targeted interventions can improve health outcomes and support healthy ageing. The main questions it aims to answer are:\n\n* Can combined frailty and intrinsic capacity screening with targeted interventions prevent or reduce functional decline in older adults, as measured by changes in life space mobility?\n* Will at least 80% of screened older adults adhere to recommended care pathways and interventions?\n* Can this screening and intervention programme demonstrate sustainability through continued community participation and recruitment of new partner organizations beyond the initial implementation phase? The investigators will compare an intervention group (receiving immediate assessment and clinical referrals based on identified needs) to a wait-list control group (receiving the same interventions 12 months later) to see if early intervention leads to better health outcomes and quality of life.\n\nParticipants will:\n\n* Attend 4 study visits over 2 years (at 6-monthly intervals in the first year, with final assessment at end of year 2), each lasting up to 2 hours.\n* Undergo comprehensive screening assessments including mobility, cognition, mental health, hearing, vision, and nutritional status.\n* Receive 2 follow-up phone calls at 3-month and 9-month intervals to monitor progress.\n* If in the intervention group: receive personalized referrals for further care (which may include comprehensive geriatric assessment, primary care reviews, rehabilitation, or dietitian consultations) and guidance on using a mobile health monitoring application.\n* If in the wait-list control group: receive the same interventions after their 3rd study visit (12 months later).",[84,85,86,87],"Frailty in Older Adults","Intrinsic Capacity","Age-related Functional Decline","Healthy Ageing",[89,90,91,92,93,94],"Frailty","Intrinsic capacity decline","Community-dwelling older adults","Age-related functional decline","Healthy ageing","Early identification and management of frailty and functional decline","2026-04-14",{"date":97,"type":34},"2026-04-17",{"date":99,"type":34},"2023-07-17",{"date":101,"type":23},"2028-01-15",{"name":40,"class":41},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":17,"sex":18,"minAge":77,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":24,"phases":112,"briefSummary":113,"conditions":114,"keywords":118,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":42},"100623430","audio-recorded-messages-delivered-via-ipad-to-prevent-delirium-in-hip-fracture-patients-100623430","NCT07396532","Audio-Recorded Messages Delivered Via iPad to Prevent Delirium in Hip Fracture Patients","Nurse-Led Audio-Recorded Reorientation to Reduce Delirium in Elderly Hip Fractures: A Pilot Randomized Control Trial","Inclusion Criteria:\n\n* Older adults aged 60 years and above\n* Undergoing hip fracture repair surgery\n* No history of cognitive impairment as assessed by Abbreviated Mental Test (AMT)\n* Able to understand to any of the basic languages of Singapore (English, Malay, Mandarin, Tamil)\n\nExclusion Criteria:\n\n* Patients not admitted directly to orthopaedic (study) wards post-operation (such as those requiring post-operative high-dependency unit care)\n* Patients managed conservatively without surgical intervention.\n* Patients admitted for periprosthetic hip fracture repairs\n* Patients who are deaf and mute",{"count":111,"type":23},30,[81],"The goal of this pilot clinical trial is to learn if personalized audio-recorded reorientation messages can be successfully implemented in general hospital wards for elderly patients after hip fracture surgery. It will also explore whether this intervention might help prevent confusion (delirium) after surgery. The main questions it aims to answer are:\n\n* Can the intervention be successfully delivered by nursing staff in a busy orthopedic ward?\n* How many eligible patients can be recruited and retained in the study?\n* Do patients tolerate listening to the personalized audio messages without problems?\n* Does listening to personalized audio messages show any early signs of reducing confusion after surgery?\n\nResearchers will compare patients who receive personalized audio messages to those who receive usual care to see if the intervention is feasible to implement and whether it shows promise for preventing delirium.\n\nParticipants will:\n\n* Listen to 2-minute personalized audio-recorded reorientation messages played through an iPad and headphones three times daily for the first 3 days after surgery\n* Have their orientation and mental status checked daily for three times by nursing staff\n* Continue with all their regular medical care and treatments\n* Be monitored until discharge from the study wards.",[115,116,117],"Delirium - Postoperative","Delirium and Post-operative Cognitive Dysfunction (POCD)","Delirium, Postoperative",[119,120,121,122],"delirium","nurse-led","reality reorientation","AI","2026-02-02",{"date":125,"type":34},"2026-02-09",{"date":127,"type":34},"2025-09-29",{"date":129,"type":23},"2026-07",{"name":40,"class":41},{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":137,"eligibilityCriteria":138,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":139,"targetDuration":4,"studyType":24,"phases":141,"briefSummary":142,"conditions":143,"keywords":146,"overallStatus":152,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":4},"100591436","post-discharge-monitoring-initiative-on-outcomes-of-post-surgical-patients-100591436","NCT06980402","Post-discharge Monitoring Initiative on Outcomes of Post-surgical Patients","Pragmatic Pilot Study of SKH@Home Post-discharge Monitoring Initiative on Outcomes of Surgical Patients","SKH@home","Inclusion Criteria:\n\n1. Patient is keen for home management\n2. Hemodynamically stable\n3. Able and willing to self-care and monitor \u002F Good social support\n4. Lives in Singapore's Northeast region\n\n   EITHER\n5. Diagnosed with intra-abdominal abscess requiring ongoing IV antibiotics as recommended by Infectious Diseases Specialist where necessary OR Diagnosed with liver abscess requiring ongoing IV antibiotics as recommended by Infectious Diseases Specialist where necessary AND Has undergone initial treatment (e.g., drainage if required) and is clinically improving\n\n   OR\n6. Underwent an uneventful straightforward bariatric surgical procedure, and has been monitored overnight without any immediate postoperative issues OR Underwent uneventful straightforward laparoscopic\u002F endoscopic\u002F minimally invasive surgery, and has been monitored for at least 6 hours without any immediate postoperative issues AND has no significant intraprocedural concerns by the operating surgeon\n\nExclusion Criteria:\n\n1. Unable to self-care \u002F no caregiver\n2. Requires daily review by the surgical team\n3. Suspicion of surgical complications requiring surgical intervention\n4. Requires post-discharge monitoring care for \\> 2 weeks\n5. Unregulated psychiatric disorders\n6. Daily flushing of drains required",{"count":140,"type":23},1000,[81],"The investigators are conducting a prospective study to evaluate the SKH@Home programme, a post-discharge monitoring initiative for surgical patients. The aim of this study is to conduct a pragmatic, non-randomized pilot study to compare the SKH@Home programme with standard post-surgical care on patient outcomes.",[144,145],"Laparoscopy","Discharge Planning",[147,148,149,150,151],"Bariatric surgery","Laparoscopic surgery","Abdominal abscesses","Liver abscesses","Discharge planning","NOT_YET_RECRUITING","2025-05-12",{"date":155,"type":34},"2025-05-20",{"date":157,"type":23},"2025-06-01",{"date":159,"type":23},"2029-01-31",{"name":40,"class":41},{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":166,"acronym":4,"eligibilityCriteria":167,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":168,"enrollmentInfo":169,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":170,"conditions":171,"keywords":176,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":42},"100544005","pilot-study-of-the-human-metagenome-in-metabolic-diseases-100544005","NCT06363253","Pilot Study of the Human Metagenome in Metabolic Diseases","Understanding the Role of the Human Metagenome in Obesity, Metabolic Diseases, Chronic Inflammation, Sarcopenia and Sarcopenic Obesity - a Pilot Study","Inclusion Criteria (obese cohort):\n\n* Obese (BMI\\>27.5kg\u002Fm2)\n\nInclusion Criteria (sarcopenic cohort):\n\n* Sarcopenic patients, defined as 1) low handgrip strength (\\\u003C26 for males; \\\u003C18kg for females), AND\u002FOR low gait speed (\\\u003C0.8m\u002Fs) AND low muscle mass (\\\u003C7.0kg\u002Fm2 for males; \\\u003C5.7kg\u002Fm2 for females)\n\nInclusion Criteria (control cohort):\n\n\\- Healthy subjects without sarcopenia, and not obese (BMI\\\u003C27.5kg\u002Fm2)\n\nExclusion Criteria:\n\n* No informed consent\n* Presence of intestinal stoma, hence inability to collect fecal samples","99 Years",{"count":79,"type":23},"This is a cohort study to understand the role of the human metagenome, and associated metabolites, in health and in various diseased states, in particular obesity as well as sarcopenia.\n\nRecruited participants will have their fecal, salivary, urine, serum, and in certain instances, mucosal samples taken, for metagenomic sequencing and metabolite testing.\n\nWe hope to uncover various differences and signatures in the metagenome and metabolome in various diseased states, with potential future therapeutic applications in personalised medicine.",[172,29,173,174,175],"Obesity","Sarcopenic Obesity","Chronic Inflammation","Metabolic Syndrome",[172,29,177,178,179],"Metabolic syndrome","Metagenomics","Metabolomics",{"date":181,"type":34},"2025-05-15",{"date":183,"type":34},"2023-08-14",{"date":185,"type":23},"2027-12-31",{"name":40,"class":41},{"id":188,"slug":189,"hasResults":11,"nctId":190,"briefTitle":191,"officialTitle":192,"acronym":4,"eligibilityCriteria":193,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":194,"enrollmentInfo":195,"targetDuration":4,"studyType":24,"phases":197,"briefSummary":198,"conditions":199,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":203,"lastUpdatePostDateStruct":204,"startDateStruct":206,"completionDateStruct":208,"leadSponsor":210,"locationsCount":42},"100519461","effectiveness-of-focused-tele-education-in-reducing-diabetes-complications-during-ramadan-100519461","NCT06043843","Effectiveness of Focused Tele-education in Reducing Diabetes Complications During Ramadan","Effectiveness of a Ramadan-focused Structured Diabetes Tele-education in Reducing Diabetes Complications During Ramadan Fasting in South East Asia","Inclusion Criteria:\n\n* Adults with diabetes planning to fast in Ramadan,\n\n  1. Adults with type 2 diabetes aged at least 21 years old,\n  2. Able to fast at least 15 days in Ramadan based on experience of fasting in previous year's Ramadan,\n  3. Underlying type 2 diabetes treated with basal insulin and one or more doses of prandial insulin, or at least twice-daily premixed insulin\n  4. Performed laboratory tests as per standard care - glycated haemoglobin (HbA1c), serum Low Density Lipoprotein- cholesterol, serum triglycerides, serum High Density Lipoprotein- cholesterol, serum Total cholesterol and serum creatinine\n  5. Ability to give informed consent,\n  6. Ability to perform self-monitoring blood glucose\n  7. Have had diabetes-related clinic visits or hospitalization in the past 10 months.\n  8. Have the capacity for video conferencing (internet connection with mobile phone or computer)\n\nExclusion Criteria:\n\n1. Severe diabetes complications including end-stage renal failure\n2. Severe hypoglycemia and hyperglycemic crises within the last 3 months\n3. Advanced comorbidities negating the ability to fast\n4. Pregnancy\n5. Patients on oral medications alone or oral medications plus basal insulin alone\n6. Patients on sulfonylureas","100 Years",{"count":196,"type":23},300,[81],"Introduction Diabetes is a global emergency with detrimental clinical and financial consequences. Poorly managed diabetes leads to a myriad of serious complications, especially cardiovascular and infectious complications, with consequent increased cost and mortality rate. For Muslims in particular, the annual fasting month of Ramadan is one such period when diabetes control is essential. Adequate adjustments in diabetes management need to be made in line with the allowed mealtimes to avoid the risk of diabetes complications during Ramadan.\n\nObjective Investigators aim to investigate the effectiveness of Ramadan-focused structured diabetes tele-education to reduce diabetes complications during Ramadan fasting for Muslims with diabetes in South East Asia.\n\nMethodology In a parallel group randomized controlled trial, investigators aim to recruit 300 adults with diabetes who are able to fast at least 15 days in Ramadan. You will be randomized to the intervention group comprising of a Ramadan-focused structured diabetes tele-education and control group receiving standard care. You will be reviewed again after Ramadan. The primary outcome is the incidence of hypoglycemia in Ramadan. The secondary outcomes are incidence of other diabetes complications in Ramadan episodes including hyperglycemia, episodes of acute infections, attendances in clinic and emergency department, hospital admissions, and compliance to recommendations for diabetes management during Ramadan.\n\nClinical Significance The study enables investigators to evaluate Ramadan-focused structured diabetes tele-education to reduce the risk of diabetes complications for a large population during the fasting month.",[200,201,202],"Diabetes Mellitus","Fasting","Diabetes Complications","2023-09-12",{"date":205,"type":34},"2023-09-21",{"date":207,"type":34},"2021-02-16",{"date":209,"type":23},"2026-06",{"name":40,"class":41},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":219,"targetDuration":4,"studyType":24,"phases":221,"briefSummary":222,"conditions":223,"keywords":227,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":237,"leadSponsor":239,"locationsCount":240},"100464685","crural-repair-during-laparoscopic-sleeve-gastrectomy-in-patients-with-a-lax-gastroesophageal-junction-100464685","NCT05330910","Crural Repair During Laparoscopic Sleeve Gastrectomy in Patients With a Lax Gastroesophageal Junction","A Randomized Controlled Trial Evaluating PAtients With Lax Gastroesophageal Junction to Initial Sleeve Gastrectomy With or Without Concomitant Crural Repair (REPAIR)","REPAIR","Inclusion Criteria:\n\n* 21-65 years old\n* Able to provide informed consent\n* Hill's grade III gastroesophageal junction on preoperative endoscopy\n* Opted to undergo laparoscopic sleeve gastrectomy as their bariatric procedure\n\nExclusion Criteria:\n\n* Unable or unwilling to provide informed consent\n* Contraindications to laparoscopic sleeve gastrectomy\n* Opted not to undergo laparoscopic sleeve gastrectomy\n* Had previous upper gastrointestinal surgery\n* Had documented erosive esophagitis on preoperative endoscopy\n* Had Hill's grade I, II or IV gastroesophageal junction on preoperative endoscopy",{"count":220,"type":23},96,[81],"Background:\n\nLaparoscopic sleeve gastrectomy (LSG) is one of the commonest bariatric procedures. However, it is associated with postoperative gastroesophageal reflux disease (GERD) and erosive esophagitis (EE). The investigators' preliminary study suggests that the incidence of postoperative GERD and EE appears to be correlated with the preoperative presence of a lax gastroesophageal flap valve and hiatal hernia.\n\nHypothesis\u002F Aim:\n\nTo investigate the impact of a concomitant hiatal hernia repair with LSG on the incidence of postoperative EE.\n\nSignificance:\n\nFor patients with pre-existing EE, most surgeons will recommend a laparoscopic Roux-en-Y gastric bypass (LRYGB) as their primary bariatric procedure. However, compared to LSG, LRYGB is a technically more demanding procedure with increased morbidity and long term nutritional deficiencies. For asymptomatic patients at risk of postoperative EE due to presence of a hiatal hernia, there is still no consensus on the most appropriate bariatric surgical option. A LSG with a concomitant hiatal hernia repair, if shown to reduce EE postoperatively, may help to expand the pool of patients suitable for LSG in the future.\n\nMethods:\n\nA two center, double-blinded, randomized controlled trial of all patients, undergoing LSG with a preoperative diagnosis of a Hill's grade III gastroesophageal junction, will be randomized to having a concomitant hiatal hernia repair (experimental arm) versus just LSG alone (control arm). Primary outcome measures include 1-year postoperative EE on endoscopy. Secondary outcome measures include postoperative morbidity, blood loss, quality of life and GERD symptoms at 1-year postoperatively.",[172,224,225,226],"Bariatric Surgery Candidate","Esophagus Injury","Gastroesophageal Reflux",[172,228,229,230,231],"Bariatric Surgery","Esophagitis","Gastroesophageal reflux disease","Laparoscopic sleeve gastrectomy","2022-04-10",{"date":234,"type":34},"2022-04-15",{"date":236,"type":34},"2022-04-01",{"date":238,"type":23},"2028-04-30",{"name":40,"class":41},2,""]