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Patients With Persistent Postoperative Pain at 3 Months","DROPS","Inclusion Criteria:\n\n* Patients who have undergone one of the following procedures:\n\n  * Inguinal hernia repair, regardless of the surgical technique used\n  * Breast reduction\n  * Mastectomy with or without reconstruction but with lymph node dissection\n  * Knee arthroscopy or knee ligamentoplasty\n\n    * Patients with a smartphone\n    * French-speaking patients\n    * Patients affiliated with a social security\n    * Patients who have given their free and informed verbal consent\n\nExclusion Criteria:\n\n* Patients with pain sensitivity defined by the presence of chronic pain, use of level 3 morphine analgesics, use of anxiolytics, gabapentinoids and\u002For antidepressants\n* Patients subject to legal protection measures\n* Patients deprived of their liberty\n* Pregnant, labouring or breastfeeding patients","ALL","18 Years",{"count":218,"type":219},2052,"ESTIMATED","INTERVENTIONAL",[222],"NA","Chronic postoperative pain has an overall incidence of approximately 30%, with 5% to 10% of cases classified as severe (numerical rating scale \\> 6\u002F10). However, its management remains suboptimal, primarily due to underdiagnosis and delayed referral of patients to specialized chronic pain centers.\n\nImproving the screening of patients with chronic postoperative pain is therefore crucial. Our research has shown that early detection of postoperative neuropathic pain is possible using just two text messages (SMS), as early as three months after surgery. Early screening, combined with prompt management, can prevent pain from becoming chronic and mitigate its harmful effects.\n\nStudy design\n\nThis study is a cluster crossover randomized trial. All participating centers (n=16) will take part in two sequential study periods:\n\n* Control Period: \"Without early treatment at 3 months\" During this period, patients with persistent postoperative pain-identified via SMS-will receive treatment at 6 months. This reflects the current standard of care for patients with postoperative pain.\n* Intervention Period: \"With early treatment at 3 months\" During this period, patients with persistent postoperative pain-identified via SMS-will receive early treatment starting at 3 months.\n\nStudy Population\n\nThe study will include patients undergoing the following minor surgical procedures:\n\n* Inguinal hernia repair\n* Breast reduction\n* Mastectomy with lymph node dissection\n* Knee arthroscopy\n* Knee ligament reconstruction\n\nStudy Schedule Recruitment Period: 24 months Patient Follow-up: 6 months Total Estimated Study Duration: 30 months",[225],"Chronic Postoperative Pain","NOT_YET_RECRUITING","2025-09-05",{"date":229,"type":230},"2025-09-08","ACTUAL",{"date":232,"type":219},"2025-11",{"date":234,"type":219},"2028-04",{"name":5,"class":6},16]