[{"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:":54},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"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":18,"type":19},72,"ESTIMATED","INTERVENTIONAL",[22],"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.",[25],"PONV",[27],"Transcutaneous Electrical Acupoint Stimulation","RECRUITING","2026-07-09",{"date":31,"type":32},"2026-07-13","ACTUAL",{"date":34,"type":32},"2018-08-01",{"date":36,"type":19},"2027-12-20",{"name":38,"class":39},"Jyoti Pandya","OTHER",1,{"id":42,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":43,"targetDuration":4,"studyType":20,"phases":44,"briefSummary":23,"conditions":45,"keywords":46,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":50,"completionDateStruct":51,"leadSponsor":53,"locationsCount":40},"100300167",{"count":18,"type":19},[22],[25],[27],"2025-03-19",{"date":49,"type":32},"2025-03-24",{"date":34,"type":32},{"date":52,"type":19},"2026-12-20",{"name":38,"class":39},""]