[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jyoti Pandya\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":55},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"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":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100054055","effect-of-teas-on-ponv-after-spinal-surgery-100054055",false,"NCT03187535","Effect of TEAS on PONV After Spinal Surgery","The Effect of Transcutaneous Electric Acupoint Stimulation on Post-operative Nausea and Vomiting After Spinal Surgery","Inclusion Criteria:\n\n* Male and female patients , 18 or older\n* American Society of Anesthesiologists (ASA) classification I or II or III\n* Undergoing elective spinal surgery expected to last no more than four hours (from induction of anesthesia to extubation).\n* Capable and willing to consent\n\nExclusion Criteria:\n\n* Neuraxial (intrathecal or epidural) block\n* Significant ongoing history of vestibular disease or dizziness\n* Nausea or vomiting within 24 hours prior to surgery, use of antiemetic or emetogenic drugs within 3 days of surgery\n* Documented alcohol or substance abuse within 3 months before the surgery\n* Limb abnormalities such as burn and amputation.\n* Poorly controlled diabetes mellitus (fasting plasma glucose \\>126 mg\u002FdL or \\\u003C70 mg\u002FdL)\n* Implantation of metal\u002Felectrical devices, such as nerve stimulator, cardiac pacemaker, cardioverter, defibrillator and internal hearing aids\n* Rash, local infection, keloid, any dermatologic condition that could interfere with the acupoint stimulation area\n* Documented alcohol or substance abuse within 3 months before surgery\n* Presence of clinically diagnosed major psychiatric condition such as bipolar disorder, uncontrolled major depression, or schizophrenia\n* Chemotherapy or radiation therapy within 7 days before surgery\n* Investigational product use within 3 months prior surgery\n* Any condition, which in the opinion of the investigator would make subject ineligible for participation in the study (history of unstable cardiovascular, pulmonary, renal, hepatic, seizures)\n* Special population (prisoners, pregnant and lactating women)","ALL","18 Years",{"count":19,"type":20},72,"ESTIMATED","INTERVENTIONAL",[23],"NA","The proposed research will utilize electroacupuncture, a type of needleless acupuncture that uses electrostimulation, in a randomized, double blind study, to evaluate the incidence of post-operative nausea and vomiting (PONV) in patients undergoing spinal surgeries with the transcutaneous electrical acupoint stimulation (TEAS) compared to patients without TEAS.",[26],"PONV",[28],"Transcutaneous Electrical Acupoint Stimulation","RECRUITING","2026-07-09",{"date":32,"type":33},"2026-07-13","ACTUAL",{"date":35,"type":33},"2018-08-01",{"date":37,"type":20},"2027-12-20",{"name":39,"class":40},"Jyoti Pandya","OTHER",1,{"id":43,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":44,"targetDuration":4,"studyType":21,"phases":45,"briefSummary":24,"conditions":46,"keywords":47,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":48,"lastUpdatePostDateStruct":49,"startDateStruct":51,"completionDateStruct":52,"leadSponsor":54,"locationsCount":41},"100300167",{"count":19,"type":20},[23],[26],[28],"2025-03-19",{"date":50,"type":33},"2025-03-24",{"date":35,"type":33},{"date":53,"type":20},"2026-12-20",{"name":39,"class":40},""]