[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"phacoemulsification\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:phacoemulsification":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,72],{"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":33,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100579601","anxiety-and-surgery-satisfaction-for-cataract-patient-with-different-state-anxiety-100579601",false,"NCT06826417","Anxiety and Surgery Satisfaction for Cataract Patient With Different State Anxiety","Pain, Anxiety and Anesthetic Satisfaction for Patient With Different State Anxiety Underwent Cataract Surgery With Topical Anesthesia","Inclusion Criteria:\n\n1. Age between 18 and 80 years old.\n2. Patients diagnosed with cataracts.\n3. Scheduled for cataract surgery with phacoemulsification and intraocular lens implantation under surface anesthesia at National Taiwan University Hospital.\n4. No adverse reactions to oral anti-anxiety medication (XANAX).\n\nExclusion Criteria:\n\n1. Presence of any contraindications for surgery before the procedure.\n2. Presence of any contraindications for medication before the procedure.\n3. Inability to provide clear and complete answers to relevant questionnaires, or expression of no preoperative anxiety during the outpatient visit, or scores below 21 on the STAI-S or STAI-T assessment.\n4. Regular use of anti-anxiety medications, sleeping pills, or analgesics before the procedure.\n5. Pregnancy or breastfeeding during the preoperative period.\n6. Severe corneal diseases, overripe cataracts, small pupils, or lens dislocation leading to difficulties in conventional surgery.\n7. Patients under surface anesthesia who cannot fully cooperate with the surgical procedure.\n8. Pregnant or uncertain pregnancy status (women under 55 years old to be verbally asked by research team members).",true,"ALL","18 Years","80 Years",{"count":21,"type":22},400,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study aims to explore the effects of anxiety traits on pain, anxiety, and anesthesia satisfaction in patients undergoing cataract surgery under topical anesthesia. On the day of recruitment, patients will complete the BAI, STAI-S, and STAI-T anxiety questionnaires to assess baseline anxiety levels. Thirty minutes before the surgery, patients will be randomly assigned, in a double-blind manner, to receive either Xanax or a placebo and will retake the BAI, STAI-S, and STAI-T questionnaires. After the surgery, patients' pain levels and anesthesia satisfaction will be evaluated, with the pain scale and satisfaction survey repeated the following day. The results will analyze the relationship between anxiety traits and pharmacological interventions on the surgical experience, aiming to optimize surgical procedures and improve overall patient comfort.",[28,29,30,31,32],"Oral Anxiolytic","Phacoemulsification","Cataract Surgery","Satisfaction Survey","State Anxiety",[34,29,35,36,32],"Oral anxiolytic","Cataract surgery","Satisfaction survey","RECRUITING","2026-04-21",{"date":40,"type":41},"2026-04-23","ACTUAL",{"date":43,"type":41},"2024-01-02",{"date":45,"type":22},"2026-12-31",{"name":47,"class":48},"National Taiwan University Hospital","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":68,"leadSponsor":70,"locationsCount":49},"100595939","non-center-involving-diabetic-macular-edema-progression-in-early-postoperative-period-after-phacoemulsification-100595939","NCT07038967","Non-Center Involving Diabetic Macular Edema Progression in Early Postoperative Period After Phacoemulsification","Assessment of Non-Center Involving Diabetic Macular Edema Progression in Early Postoperative Period After Phacoemulsification","Inclusion Criteria:\n\n* Age ≥18 years.\n* Both sexes.\n* Patients with Grade I - Grade II nuclear cataract and non-center-involving diabetic macular edema (NCIDME).\n\nExclusion Criteria:\n\n* Traumatic cataract.\n* Severe Non-Proliferative\u002F Proliferative Diabetic Retinopathy.\n* Marked Asymmetry of retinopathy between both eyes.\n* Mature senile cataract or severe lens opacity.\n* Potentiality to have Phacotrabeculectomy surgery.\n* Complications during or after the surgery.",{"count":58,"type":22},50,"OBSERVATIONAL","This study aims to evaluate the progression of non-center-involving diabetic macular edema in the early postoperative period following phacoemulsification.",[62,63,29],"Non-Center","Diabetic Macular Edema","2025-06-29",{"date":66,"type":41},"2025-07-01",{"date":64,"type":41},{"date":69,"type":22},"2025-12-01",{"name":71,"class":48},"Ain Shams University",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":23,"phases":80,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":85,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":4},"100584976","phase-1-effectiveness-and-safety-of-limbal-relaxing-incisions-for-correcting-post-phacoemulsification-high-astigmatism-100584976","NCT06896357","Effectiveness and Safety of Limbal Relaxing Incisions for Correcting Post Phacoemulsification High Astigmatism","Inclusion Criteria:\n\n* Conventional phacoemulsification was done at least one month earlier.\n* Clear cornea with corneal astigmatism more than 3.0 D.\n\nExclusion Criteria:\n\n* History of corneal surgeries (e.g., keratoplasty, refractive surgery, and corneal wound repair).\n* Ocular trauma.\n* Other intraocular surgery.\n* Patient with corneal opacities.\n* Thin cornea .\n* Any significant ocular disease causing diminution of vision (e.g., optic atrophy, diabetic retinopathy, and age-related macular degeneration), autoimmune disease, and peripheral corneal disease.",{"count":79,"type":22},30,[81],"PHASE1","To compare the effect of Limbal relaxing incisions (LRIs) plus spectacle correction versus spectacle correction alone on subjective and objective improvement in visual function for correcting post phacoemulsification high astigmatism .",[84,29],"Astigmatism","NOT_YET_RECRUITING","2025-03-24",{"date":88,"type":41},"2025-03-26",{"date":90,"type":22},"2025-05-01",{"date":92,"type":22},"2026-06-01",{"name":94,"class":48},"Assiut University"]