[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"traditional-chinese-medication-tcm\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:traditional-chinese-medication-tcm":28},{"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":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100599231","the-effect-of-perioperative-transcutaneous-electrical-acupoint-stimulation-combined-with-traditional-chinese-medicine-on-gastrointestinal-function-recovery-in-patients-undergoing-abdominal-surgery-100599231",false,"NCT07081802","The Effect of Perioperative Transcutaneous Electrical Acupoint Stimulation Combined With Traditional Chinese Medicine on Gastrointestinal Function Recovery in Patients Undergoing Abdominal Surgery","the Effect of Perioperative Transcutaneous Electrical Acupoint Stimulation Combined With Traditional Chinese Medicine on Gastrointestinal Function Recovery in Abdominal Surgery Patients","Inclusion Criteria:\n\n* Patients aged \\>18 years with no severe preoperative gastrointestinal dysfunction (e.g., no chronic gastrointestinal diseases such as long-term constipation or diarrhea).\n* Scheduled abdominal Grade IV surgeries (limited to liver, gallbladder, pancreas, stomach, or intestinal procedures) performed via open or laparoscopic approach.\n* Preoperative American Society of Anesthesiologists (ASA) Physical Status Classification of I-III.\n* Patients and their families fully understand the study's purpose, methods, potential risks\u002Fbenefits, and provide signed informed consent.\n\nExclusion Criteria:\n\n* Comorbid severe systemic diseases.\n* Local skin abnormalities at acupoints (e.g.,broken skin, infection, allergies, or scarring).\n* Preoperative long-term use (\\>1 month) of gastrointestinal motility-affecting drugs (e.g., mosapride, domperidone) that cannot be discontinued, or allergies to TCM components\u002Felectrode materials.\n* Psychiatric disorders or cognitive impairment rendering patients unable to comply with the study.\n\nElimination Criteria:\n\n* Non-compliance with treatment protocols (e.g., receiving \\\u003C80% of planned sessions).\n* Significant missing data.\n* Occurrence of severe adverse events unrelated to the study intervention.","ALL","18 Years","80 Years",{"count":20,"type":21},148,"ESTIMATED","INTERVENTIONAL",[24],"NA","Protocol Summary Project Name:Effect of Perioperative TEAS Combined with TCM on Gastrointestinal Function Recovery in Abdominal Surgery Patients Research Objective:To evaluate the impact of perioperative TEAS combined with TCM on postoperative gastrointestinal function, pain, adverse reactions, hospital stay, and complications, as well as its safety, aiming to enrich the ERAS and prehabilitation theory and promote the integration of TCM in surgical practice.\n\nResearch Design:Prospective, randomized, open-label trial involving 148 abdominal surgery patients (Grade IV surgeries) randomly assigned 1:1 to the experimental group (TCM + TEAS + prehabilitation + ERAS) or the control group (prehabilitation + ERAS).\n\nTotal Cases:148 Case Selection\n\nInclusion Criteria:\n\n1. Age 18-80, no severe gastrointestinal dysfunction;\n2. Elective abdominal Grade IV surgeries (pancreas or colorectall surgeries) via open or laparoscopic methods;\n3. Preoperative ASA classification I-III;\n4. Signed informed consent.\n\nExclusion Criteria:\n\nSevere comorbidities, skin abnormalities at acupoints, long-term use of gastrointestinal motility drugs, or other factors affecting the trial.\n\nElimination Criteria:\n\nPoor compliance, significant missing data, or severe adverse events unrelated to the intervention.\n\nTreatment Plan TEAS combined with TCM from the day of surgery to postoperative day 4, alongside prehabilitation and ERAS.\n\nEfficacy Evaluation\n\nPrimary Outcomes:\n\nTime to first flatus and defecation.\n\nSecondary Outcomes:\n\nPostoperative hospital stay, time to tolerate semi-liquid\u002Fsolid food, nausea\u002Fvomiting, pain, bloating, first ambulation, 30-day readmission rate, WBC\u002FCRP levels, and gastrin levels.\n\nSafety Evaluation: Any adverse events. Statistical Methods Continuous variables expressed as mean (SD) or median (IQR); independent t-test for normal distributions. Categorical variables summarized as frequencies\u002Fpercentages, analyzed using χ² or Fisher's exact test. Group differences reported as 95% CI and two-sided P-values (P \\\u003C 0.05 significant). Preset subgroup analyses by surgery type and frailty.",[27,28],"ERAS","Traditional Chinese Medication (TCM)","RECRUITING","2026-05-30",{"date":32,"type":33},"2026-06-02","ACTUAL",{"date":35,"type":33},"2025-09-01",{"date":37,"type":21},"2026-09-28",{"name":39,"class":40},"Guang'anmen Hospital of China Academy of Chinese Medical Sciences","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":22,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":5},"100590805","reflexology-massage-and-hot-water-foot-bath-for-pain-and-gi-recovery-after-colorectal-surgery-100590805","NCT06972199","Reflexology Massage and Hot Water Foot Bath for Pain and GI Recovery After Colorectal Surgery","The Effect of Reflexology Massage and Hot Water Foot Bath on Pain and Gastrointestinal Functions After Colorectal Surgery","Inclusion Criteria:\n\n* 18 years of age or older,\n* Planning laparoscopic surgery for a malignant tumour in the large intestine,\n* The same method was used for preoperative bowel and GI tract preparation,\n* Postoperative Numerical Proportioning Scale (NRS) score of 3 and above,\n* Verbal and written acceptance to participate in the research.\n\nExclusion Criteria:\n\n* The patient has a temporary or permanent stoma,\n* Having a history of reflexology application before,\n* Open wound, infection, circulatory disorder, lesion, etc. in the areas where reflexology massage or hot water foot bath will be applied,\n* Patient-controlled analgesia in the early postoperative period\n* Having any problem that prevents verbal communication.",{"count":50,"type":21},102,[24],"This study was planned to examine the effect of non-invasive treatment methods that can be applied to alleviate complications involving gastrointestinal system functions such as pain, nausea, vomiting, and absence of gas\u002Ffaecal output after colorectal (colon and rectum) cancer surgery. The two main intervention methods of the study were reflexology massage and hot water foot bath. The effects of these methods on reducing postoperative pain and improving gastrointestinal functions will be investigated. The study was planned as a randomised controlled experimental study to determine the effects of reflexology massage and hot water foot bath on postoperative pain and gastrointestinal functions in colorectal cancer patients undergoing laparoscopic surgery. It is thought that the study will provide evidence for determining the appropriate method to reduce pain and improve gastrointestinal functions in patients undergoing colorectal cancer surgery. The population of the study will consist of colorectal cancer patients who will undergo laparoscopic surgical intervention who are admitted to the General Surgery Clinic of SBU Istanbul Ümraniye Training and Research Hospital.\n\nBased on the percentage measurement values of the methods to be studied in the literature review, G-POWER programme was used for sample calculation with an effect size of 0.4 (Cohen), 95% power and 0.05% margin of error. Cohen\\'s standard effect size was taken as the basis for the effect size. The calculated value is the total value for 3 groups and the total sample size for 3 groups was found as n=102. The number of samples per group was determined as (n)=34. In order to prevent bias in the study, patients who meet the study criteria will be distributed to the experimental and control groups by computerised randomisation programme. Data will be collected by using the Patient Information Form consisting of two parts, Rhodes Nausea, Vomiting and Retching Index and Numerical Proportioning Scale (NRS) developed by the researcher in line with the literature. The data obtained will be evaluated with appropriate statistical methods in the licensed SPSS 21.0 package programme.",[54,55,28,56],"Colorectal Surgery","Reflexology","Nursing","2025-05-07",{"date":59,"type":33},"2025-05-14",{"date":61,"type":33},"2024-10-30",{"date":63,"type":21},"2026-06-30",{"name":65,"class":40},"Istanbul University - Cerrahpasa"]