[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jingping Wang, MD, Ph.D.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":85},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,37,58],{"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":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":4},"100620557","delivery-mode-impact-on-postoperative-depression-100620557",false,"NCT07359170","Delivery Mode Impact on Postoperative Depression","Impact of Elective Versus Emergency Cesarean Delivery on Early Postpartum Depression: a Retrospective Study","Inclusion Criteria:\n\nUnderwent cesarean delivery (elective or emergency) or vaginal delivery during the study period\n\nAge 18 years or older\n\nCompleted at least one Edinburgh Postnatal Depression Scale (EPDS) assessment at 6-8 weeks postpartum\n\nHave complete perioperative data available\n\nExclusion Criteria:\n\nMissing 6-8 week postpartum EPDS scores\n\nPregnancy with fetal demise, severe obstetric complications, or atypical maternal conditions\n\nHistory of severe psychiatric disorders (e.g., schizophrenia, bipolar disorder), when identifiable\n\nIncomplete perioperative medical records","FEMALE","18 Years",{"count":19,"type":20},4000,"ESTIMATED","OBSERVATIONAL","The goal of this observational retrospective cohort study is to examine the association between mode of delivery and early postpartum depressive symptoms in adult women who delivered at Massachusetts General Hospital. Specifically, the study evaluates whether the urgency of cesarean delivery (elective versus emergency) is associated with differences in Edinburgh Postnatal Depression Scale (EPDS) scores at 6-8 weeks postpartum, compared with elective cesarean delivery and vaginal delivery. The EPDS is a validated 10-item self-report questionnaire with scores ranging from 0 to 30, where higher scores indicate more severe depressive symptoms.\n\nThe primary questions are whether EPDS scores differ among women undergoing emergency cesarean delivery, elective cesarean delivery, and vaginal delivery, and whether perioperative and obstetric factors are associated with postpartum depressive symptoms.\n\nThis study involves retrospective analysis of de-identified electronic health record data. Participants will not undergo any study-specific interventions.",[24],"Postoperative Depression","NOT_YET_RECRUITING","2026-06-06",{"date":28,"type":29},"2026-06-09","ACTUAL",{"date":31,"type":20},"2026-10-15",{"date":33,"type":20},"2027-12-28",{"name":35,"class":36},"Jingping Wang, MD, Ph.D.","OTHER",{"id":38,"slug":39,"hasResults":11,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":4,"eligibilityCriteria":43,"healthyVolunteers":11,"sex":44,"minAge":17,"maxAge":45,"enrollmentInfo":46,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":48,"conditions":49,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":51,"startDateStruct":52,"completionDateStruct":54,"leadSponsor":56,"locationsCount":57},"100620554","postoperative-assessment-of-platelet-rich-plasma-and-platelet-rich-fibrin-in-temporomandibular-joint-surgery-100620554","NCT07359131","Postoperative Assessment of Platelet-Rich Plasma and Platelet-Rich Fibrin in Temporomandibular Joint Surgery","Postoperative Assessment in TMJ Surgery: A Comparison of the Efficacy of Intraoperative Platelet-Rich Plasma and Platelet-Rich Fibrin Injections","Inclusion Criteria:\n\nPatients aged 18 to 75 years (inclusive)\n\nUnderwent unilateral or bilateral temporomandibular joint (TMJ) arthroscopy\n\nReceived intraoperative platelet-rich plasma (PRP) or platelet-rich fibrin (PRF) injection during TMJ arthroscopy\n\nExclusion Criteria:\n\nAge younger than 18 years or older than 75 years\n\nDid not undergo TMJ arthroscopy\n\nDid not receive intraoperative PRP or PRF injection\n\nIncomplete clinical or follow-up data","ALL","75 Years",{"count":47,"type":20},700,"The goal of this observational study is to evaluate postoperative outcomes following temporomandibular joint (TMJ) surgery and to compare the effectiveness of intraoperative platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) injections in patients with temporomandibular joint disorders.\n\nThe study includes adult patients who underwent TMJ surgery and received either PRP or PRF intraoperatively. The main questions this study aims to answer are:\n\nWhether intraoperative PRP or PRF injection is associated with differences in postoperative pain intensity and recovery.\n\nWhether PRP and PRF differ in their effects on postoperative jaw function, including maximum mouth opening and joint symptoms.\n\nIf there is a comparison group: Researchers will compare patients who received intraoperative PRP with those who received intraoperative PRF to assess differences in postoperative pain, functional outcomes, and joint-related symptoms.\n\nParticipants will:\n\nHave their existing medical records reviewed retrospectively.\n\nProvide postoperative outcome data derived from routine clinical follow-up, with no prospective recruitment or intervention.",[50],"Temporomandibular Joint Disorders",{"date":28,"type":29},{"date":53,"type":20},"2026-11-15",{"date":55,"type":20},"2027-12-05",{"name":35,"class":36},1,{"id":59,"slug":60,"hasResults":11,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":4,"eligibilityCriteria":64,"healthyVolunteers":11,"sex":44,"minAge":17,"maxAge":4,"enrollmentInfo":65,"targetDuration":4,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":57},"100608142","imagined-acupuncture-for-postoperative-pain-after-spinal-surgery-100608142","NCT07197710","Imagined Acupuncture for Postoperative Pain After Spinal Surgery","Assessing the Efficacy of Imagined Acupuncture for Postoperative Acute Pain Management in Spinal Surgery","Inclusion Criteria:\n\n* Undergoing 1- to 2-level primary spine surgery\n* Aged 18 years or older\n* Willing and able to receive postoperative imagined acupuncture (VGAIT)\n* Able to provide written informed consent\n\nExclusion Criteria:\n\n* Undergoing revision surgery or procedures involving more than 3 spinal levels\n* History of prior spinal surgery\n* Intraoperative complications likely to interfere with postoperative pain assessment\n* Diagnosed with severe cognitive impairment or psychiatric disorders that impair participation or communication\n* Pregnant or breastfeeding\n* Unable to cooperate with treatment or pain assessments Individuals with uncorrectable vision impairment that would interfere with viewing study videos or completing study questionnaires.",{"count":66,"type":20},120,"INTERVENTIONAL",[69],"NA","The goal of this clinical trial is to evaluate whether imagined acupuncture can reduce postoperative acute pain in adult patients undergoing spinal surgery. The main questions it aims to answer are:\n\nDoes video-guided imagined acupuncture improve postoperative pain control?\n\nDoes the intervention reduce opioid consumption and improve functional recovery in the immediate postoperative period?\n\nResearchers will compare the imagined acupuncture group to the control education video group to see if imagery-based intervention leads to better pain outcomes and reduced analgesic use.\n\nParticipants will:\n\nWatch a 30-minute video once daily for 7 consecutive days after surgery\n\nComplete pain and function assessments during the hospital stay and postoperative follow-up",[72],"Pain Management",[74,75],"Postoperative Acute Pain","Imagined Acupuncture","RECRUITING","2026-06-04",{"date":79,"type":29},"2026-06-08",{"date":81,"type":29},"2025-10-01",{"date":83,"type":20},"2026-09-19",{"name":35,"class":36},""]