[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Dr Hamail Khanum\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100596612","comparative-outcome-of-early-and-standard-oral-feeding-after-emergency-bowel-surgery-100596612",false,"NCT07047729","COMPARATIVE OUTCOME OF EARLY AND STANDARD ORAL FEEDING AFTER EMERGENCY BOWEL SURGERY","Inclusion Criteria:\n\n* Either Gender\n* Requiring emergency surgery due to conditions such as obstructive bowel disease, GI perforation, colorectal surgery, blunt abdominal trauma (resulting from falls or roadside accidents), and penetrating abdominal trauma (involving firearm injuries and stab wounds).\n\nExclusion Criteria:\n\n* Patients with terminal cancer need palliative surgery (as their focus is on comfort care rather than surgical intervention).\n* Patients who had undergone surgery within the past 30 days (to avoid potential complications associated with recent surgical procedures).\n* Patients receive regular renal replacement therapy (to prevent additional stress on their medical condition).\n* Pregnant women (as surgical interventions may pose risks to both the mother and the unborn child).","ALL","18 Years",{"count":18,"type":19},60,"ESTIMATED","INTERVENTIONAL",[22],"NA","Informed consent will be obtained from patients or their legal representatives in cases where the patient is unconscious. Patient information, including names, ages, gender, smoking history, comorbidities, and the indication for emergency surgical procedures, will be documented. All surgical procedures will follow standard protocols and will be conducted by a single surgical team led by at least two consultants, each with more than five years of experience. All 60 patients will be randomly allocated into two groups using a random number table: Group A (early oral feeding), consisting of 30 patients, and Group B (standard oral feeding), consisting of 30 patients. In Group A, a liquid diet will be initiated within 24 hours after surgery and, if well-tolerated without vomiting, will transition to a regular diet over the subsequent 24 hours. On the other hand, in Group B, a standard diet (late feeding), including liquid filtrates, will only be introduced after the resolution of the ileus, during which these patients will remain NPO (nothing by mouth).",[25,26,27],"Bowel Surgery","Emergency Abdominal Surgery","ERAS","RECRUITING","2025-06-24",{"date":31,"type":32},"2025-07-02","ACTUAL",{"date":34,"type":32},"2025-03-06",{"date":36,"type":19},"2025-09-06",{"name":38,"class":39},"Dr Hamail Khanum","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":15,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":20,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":40},"100589711","prophylactic-negative-pressure-wound-therapy-in-laparotomy-wounds-a-randomized-clinical-trial-100589711","NCT06957964","Prophylactic Negative Pressure Wound Therapy in Laparotomy Wounds: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Patients of age between 20 to 70 years, both genders\n* Undergoing laparotomy under general anaesthesia\n* ASA I-II\n\nExclusion Criteria:\n\n* Patients who did not complete the follow up instructions\n* Pregnant patients\n* Patients already undergone a relook laparotomy, if their abdomen is left open or if unable to adhere","20 Years","70 Years",{"count":50,"type":19},70,[22],"Total 70 participants meeting selection criteria will be enrolled in the study from operational theatre. They will be randomly divided in two groups by using lottery method. In group A, Negative Pressure Wound Therapy will be applied at end of procedure. In group B, no Negative Pressure Wound Therapy will be placed. They will be shifted to post-surgical wad for 72 hours and then will be discharged with prescription of standard antibiotics and will be followed-up in OPD for 30 days. If patient will develop surgical site wound infection, then it will be noted. If infection will not be cured with antibiotics course, then re-operation will be done. Patients complications will be managed as per hospital protocol. All this information will be recorded in proforma.",[54,55,56],"Wound","Infection Prevention","Negative Pressure Wound Therapy","2025-04-27",{"date":59,"type":32},"2025-05-06",{"date":61,"type":32},"2025-03-25",{"date":63,"type":19},"2025-06-25",{"name":38,"class":39},""]