[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"B.P. Koirala Institute of Health Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":114},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,41,66,91],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":4},"100651322","effect-of-intracuff-dexamethasone-on-postoperative-sore-throat-in-patients-undergoing-laparoscopic-cholecystectomy-100651322",false,"NCT07760272","Effect Of Intracuff Dexamethasone On Postoperative Sore Throat In Patients Undergoing Laparoscopic Cholecystectomy","EFFECT OF INTRACUFF DEXAETHASONE ON POSTOPERATIVE SORE THROAT IN PATIENTS UNDERGOING LAPAROSCOPIC CHOLECYSTECTOMY","Inclusion Criteria:\n\n* Patient aged 18-65 years.\n* Either sex\n* ASA physical status I or II\n* Mallampatti grade I and II.\n* Patient scheduled for elective laparoscopic cholecystectomy\n* Patient requiring general anesthesia with endotracheal intubation\n* Expected duration of surgery \\\u003C2 hours.\n* Patients \u002Fpatient's family member who provide written informed consent.\n\nExclusion Criteria:\n\n* Refusal for consent\n\n  * Mallampati grade III or IV\n  * More than two attempts at endotracheal intubation.\n  * Reintubation\n  * Use of bougie or stylet for intubation.\n  * Evidence of traumatic intubation (blood stained secretions or blood on ETT cuff)\n  * Preexisting sore throat, hoarseness of voice or upper respiratory tract infection.\n  * Patient receiving systemic or inhaled steroids.\n  * Known case of allergy to dexamethasone.",true,"FEMALE","18 Years","65 Years",{"count":21,"type":22},40,"ESTIMATED","INTERVENTIONAL",[25],"NA","Postoperative sore throat is the most common complication following general anesthsia with endotracheal intubation with incidence ranging from 21 to 65% Although usually self-limiting, it significantly affects patient's comfort, satisfaction and may adversely affect the quality of recovery in postoperative period.\n\nLaparoscopic cholecystectomy is one of the most performed laparoscopic surgeries and is routinely carried out under general anesthesia with endotracheal intubation. Several factors associated with this procedure like mechanical manipulation of airway during laryngoscopy and intubation, prolonged pressure of endotracheal tube cuff on the tracheal mucosa, pneumoperitoneum and positional changes during surgery may increase the risk of postoperative airway irritation and inflammation leading to sore throat, cough, hoarseness of voice.\n\nvarious methods have been used for prevention of postoperative sore throat including topic local anesthetics, lubricants and systemic corticosteroid. Among sytemic steroid, Dexameathsone has shown to reduce airway inflammation and postoperative airway complications. However systemic administration may be associated with adverse effects such as hyperglycaemia, immunosupression and delayed wound healing.\n\nIntracuff administration of dexamethasone provides an alternative approach that may help reduce postoperative airway complications while minimising systemic exposure. In this approach drug is instilled into the endotracheal tube cuff, causing it to gradually diffuse across the cuff membrane exerts local anti- inflammatory effect on the tracheal mucosa, thereby reducing inflammation and irritation exerts local anti- inflammatory effect on the tracheal mucosa, thereby reducing inflammation and irritation.\n\nThis study aims to evaluate the effect of intracuff dexamethasone on the incidence and severity of postoperative sore throat in patients undergoing laparoscopic cholecystectomy. The primary objective is to compare the incidence of postoperative sore throat between patients receiving intracuff dexamethasone and those receiving intracuff normal saline. Secondary objective includes comparing the severity of postoperative sore throat as well as the incidence and severity of postoperative cough and hoarseness of voice assessed within first 24 hours of surgery.\n\nThe study will be conducted as a prospective, double blind randomised controlled trial in the routine operation theatre of BP Koirala Institute of Health Sciences(BPKIHS),Dharan, Nepal. A total of 40 adult patients aged 18-65 years with ASA PS I or II and scheduled for elective laparoscopic cholecystectomy will be included. Participants will be randomly allocated in two groups in a ratio of 1:1. In the intervention group, cuff will be inflated with dexamethasone(0.01mg\u002Fg) diluted with normal saline, while in control group the cuff will be inflated with normal saline alone.\n\nPostoperative sore throat, cough and hoarseness of voice will be assess at 2,6, 12 and 24 hours after extubation using standardised grading scale. Data will be analysed using SPSS software and MS Excel.\n\nContinuous variables will be compared using the independent t test while the categorical variables will be analysed using the chi-square test or Fisher's test. A P value of\\\u003C0.05 will be considered statistically significant.\n\nEthical approval will be obtained from the IRC of BPKIHS and NHRC. This study may help identify a simple and cost effective strategy to reduce postoperative airway discomfort and improve patient recovery after laparoscopic cholecytectomy.",[28],"Postoperative Sore Throat, Cough, Hoarseness","NOT_YET_RECRUITING","2026-08-07",{"date":32,"type":33},"2026-08-12","ACTUAL",{"date":35,"type":22},"2027-05",{"date":37,"type":22},"2027-06",{"name":39,"class":40},"B.P. Koirala Institute of Health Sciences","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":4,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":65},"100501068","effect-of-altitude-on-postdural-puncture-headache-after-caesarean-delivery-100501068","NCT05804448","Effect of Altitude on Postdural Puncture Headache After Caesarean Delivery","Effect of Altitude on Postdural Puncture Headache After Caesarean Delivery: a Prospective, Multicentre Cohort Study","Inclusion Criteria:\n\n* Parturient, aged more than or equal to 18 years\n* American society of Anesthesiologist 2 and 3\n* Scheduled for elective and non-elective (category 2 \\& 3) caesarean delivery with spinal anesthesia\n* Native to their resident altitude i.e., those born, raised, and have continuously lived at the same altitude, at least for the past 1 year.\n\nExclusion Criteria:\n\n* Hypertensive disorder\n* Cerebrovascular disease\n* Mental disorder (schizophrenia and other psychotic disorders)\n* Known fetal anomalies\n* Contraindication to spinal anaesthesia.\n* Those requiring general anaesthesia for delivery due to failed spinal anesthesia\n* Major post-delivery complications (severe haemorrhage, sepsis, or ICU admission)\n* Those who migrate from their resident altitude (either low to high or vice versa) within 7 days post-delivery will also be excluded.",{"count":49,"type":22},292,"OBSERVATIONAL","The aim of this study is to examine the effects of altitude (high altitude versus low altitude) on incidence and severity of postural puncture headache (PDPH) following spinal anaesthesia for caesarean delivery. The investigators hypothesized that the risk of PDPH would be higher in highlander parturients than in lowlander parturients.",[53],"Post-Dural Puncture Headache",[55],"Spinal Anesthesia, Cesarean Section","RECRUITING","2025-09-16",{"date":59,"type":33},"2025-09-19",{"date":61,"type":33},"2023-04-18",{"date":63,"type":22},"2026-04-20",{"name":39,"class":40},2,{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":70,"acronym":4,"eligibilityCriteria":71,"healthyVolunteers":16,"sex":72,"minAge":18,"maxAge":4,"enrollmentInfo":73,"targetDuration":4,"studyType":23,"phases":75,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},"100570937","comparison-of-clinical-efficacy-of-submucosal-dexamethasone-and-oral-trypsin-chymotrypsin-for-reduction-of-postoperative-sequelae-after-lower-third-molar-surgery-100570937","NCT06713733","Comparison of Clinical Efficacy of Submucosal Dexamethasone and Oral Trypsin-chymotrypsin for Reduction of Postoperative Sequelae After Lower Third Molar Surgery","Inclusion Criteria:\n\n* Clinically healthy patients (ASA I) patient free of any systemic diseases that could interfere with wound healing or surgical operation.\n* Free of any recent anti-inflammatory drug intake or being under long term treatment with medicaments that will obscure the assessment of the inflammatory response as NSAIDs, steroids, or antihistamines\n* Free from allergy to the drugs used in the study\n* Patients requiring surgical removal of the mandibular impacted third molar\n\nExclusion Criteria:\n\n* Patients who are ASA II to ASA VI.\n* Patients already on corticosteroids through any route.\n* Patients with known allergy to any drugs.\n* Pregnant and lactating females\n* Patient not consenting to participate in the study","ALL",{"count":74,"type":22},50,[25],"Pain, edema and trismus are the most frequent postoperative sequelae to surgical removal of impacted teeth, all of are due to the local inflammatory response.\n\nUse of corticosteroids decrease tissue mediators of inflammation and reduce edema.\n\nUse of trypsin-chymotrypsin elaborates the enzymes esterase in blood plasma that inhibits inflammation by hydrolytic degradation of the inflammatory peptides.",[78],"Clinical Efficacy of Submucosal Dexamethasone and Oral Trypsin Chymotrypsin for Reduction of Postoperative Sequelae After Lower Third Molar Surgery",[80,81],"Dexamethasone","Trypsin-chymotrypsin","2024-11-27",{"date":84,"type":33},"2024-12-03",{"date":86,"type":33},"2024-09-25",{"date":88,"type":22},"2025-01-25",{"name":39,"class":40},1,{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":16,"sex":72,"minAge":18,"maxAge":98,"enrollmentInfo":99,"targetDuration":4,"studyType":23,"phases":101,"briefSummary":103,"conditions":104,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":4},"100528393","phase-4-comparative-assessment-of-preoperative-versus-postoperative-submucosal-dexamethasone-on-postoperative-complications-following-surgical-extraction-of-mandibular-third-molar-randomized-controlled-trial-100528393","NCT06160180","Comparative Assessment of Preoperative Versus Postoperative Submucosal Dexamethasone on Postoperative Complications Following Surgical Extraction of Mandibular Third Molar: Randomized Controlled Trial","Randomized Controlled Trial on Assessment of Preoperative Versus Postoperative Submucosal Dexamethasone On Postoperative Complications Following Surgical Extraction Of Mandibular Third Molar.","Inclusion Criteria:\n\n* Clinically healthy patients (American Society of Anesthesiology I) with impacted lower third molar.\n* Age ≥18 to ≤ 55 years\n* No history of previous pericoronitis\n\nExclusion Criteria:\n\n* • Patients who are ASA II to ASA VI.\n\n  * Patients already on corticosteriods through any route.\n  * Patients with known allergy to any drugs.\n  * Pregnant and lactating females\n  * Patient not consenting to participate in the study","55 Years",{"count":100,"type":22},60,[102],"PHASE4","The goal of this study is to compare the pain, edema and trismus of pre-operative versus post-operative submucosal dexamethasone in lower third molar surgical extraction done in healthy population.This is comparative study, will be conducted in patient indicated for surgical extraction of mandibular third molar at the department of oral and maxillofacial surgery, college of dental surgery, BPKIHS, Nepal. Verbal and written informed consent will be taken. Participants meeting inclusion criteria will be included in the study and will be divided into two groups, group A(pre-operative submucosal 2ml of 4mg\u002Fml dexamethasone will be administered prior to placing an incision in buccal vestibule) and groupB(post-operative submucosal 2ml of 4mg\u002Fml dexamethasone will be administered soon after closure of the incision site).Baseline measurement of interincisal distance for mouth opening, distance between the tragus to corner of mouth, gonion to corner of mouth and outer canthus to gonion as baseline for edema taken prior extraction. Extraction is carried out using standard protocol and postoperative antibiotics and analgesics are given. Rescue analgesic tramadol is prescribed and asked to be taken only pain score exceeds 7.Patient is kept on follow up for 2nd, 5th and 7th days and assessment of pain using numeric visual analogue scale, swelling using facial and trismus using interincial measurements and recorded. Any adverse effect of drugs will be recorded. The data collected will be entered in Microsoft excel sheet. It will then be transferred into SPSS(Statistical package for Social Sciences) for statistical analysis.",[105],"Pain, Postoperative","2024-08-07",{"date":108,"type":33},"2024-08-09",{"date":110,"type":22},"2024-08",{"date":112,"type":22},"2024-12",{"name":39,"class":40},""]