[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gelscom SAS\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":66},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100317682",false,"NCT03415828","Ethanol Gel Versus Steroid in Refractory Lumbar Discogenic Pain","Intradiscal Gelified Ethanol Versus Intradiscal Steroid in Refractory Lumbar Discogenic Pain: a Randomized Single-blind Study","IDIS","Inclusion Criteria:\n\n* Patient 18 years of age or older;\n* 2-month refractory pain to conservative treatment, non-surgical patients;\n* Chronic discogenic pain (1 or 2 lumbar discs) with concordant MR imaging;\n* Symptomatic for at least 8 weeks despite appropriate medical treatment;\n* Patient who agrees to participate in the study and who signed the informed consent form;\n* Patient with social protection.\n\nExclusion Criteria:\n\n* Previous surgical treatment of the studied disc(s);\n* Patient with pure radicular pain;\n* Sick leave of more than 12 months secondary to the symptoms;\n* Patients who cannot read or write French;\n* History of cognitive-behavioral disorders that could interact with assessment by self-questionnaire;\n* Local or general infection, or suspicion of infection;\n* Severe coagulation disorders;\n* Other rheumatic inflammatory disease;\n* Undercurrent serious pathology with life expectancy \\\u003C 2 years;\n* Female of childbearing age that are known to be pregnant during inclusion visit or wishing to become pregnant before treatment;\n* Subject who has forfeited their freedom by administrative or legal award, or is under guardianship or under limited judicial protection\n* Patient participating in another interventional clinical trial or testing an experimental drug within 30 days of inclusion in the study.","ALL","18 Years",{"count":19,"type":20},230,"ESTIMATED","INTERVENTIONAL",[23],"NA","DISCOGEL® is on the market since 2007. About 20,000 kits were sold to date (October 2017). The device re-obtained its CE mark in 2017.\n\nA clinical evaluation was performed by bibliographic route in 2016. Clinical data on more than 600 patients treated by DISCOGEL® were analyzed. These data should be confirmed by monitoring on the long term, with a large cohort of patients, over a two-year follow-up period.\n\nAs part of the post-CE surveillance, the manufacturer GELSCOM is responsible of this \"Post-Market Clinical Follow-up\" (PMCF) study in accordance with Directive 93\u002F42\u002FEEC and MEDDEV guide 2.12\u002F2, to assess the efficacy and the long-term safety of DISCOGEL®.\n\nThe study is comparative. The results will evaluate the performance and safety of the CE-marked medical device used in \"real life\", in comparison with a steroid infiltration, used according to its indication and to the current standards. It will include economic data. Patients and evaluators will be blinded. Both DISCOGEL® and HYDROCORTANCYL 2,5 POUR CENT are authorized products used according to their intended use.\n\nThis is an interventional, prospective, national, multi-center, comparative, randomized, single-blind (patient and evaluator) post-market clinical study. The primary objective is to compare the short-term efficacy profile of DISCOGEL® versus intradiscal steroid.",[26],"Lumbar Discogenic Pain (Disorder)","RECRUITING","2025-09-23",{"date":30,"type":31},"2025-09-29","ACTUAL",{"date":33,"type":31},"2018-05-29",{"date":35,"type":20},"2027-05-29",{"name":37,"class":38},"Gelscom SAS","INDUSTRY",5,{"id":41,"slug":4,"hasResults":10,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":50,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":5},"100513739","NCT05969392","Evaluation of Efficacy and Safety of Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain","Intradiscal Gelified Ethanol in Refractory Cervical Discogenic Pain : a Interventional, Prospective, Multi-center, Open-label Study.","DISCOCERV","Inclusion Criteria:\n\n* Patient 18 years or older;\n* Pain refractory to conservative treatments for more than 2 months, non-surgical patients\n* Cervicobrachialgia due to disc herniation\n* Chronic discogenic pain (1 or 2 cervical discs) with concordant MRI;\n* Patient agreeing to participate in the study and having given written consent;\n* Patient enrolled in a health insurance plan.\n\nExclusion Criteria:\n\n* Prior surgical treatment of the disc(s) studied;\n* Sick leave of more than 12 months secondary to painful symptoms;\n* Patient with Modic 1 score or more\n* History of cognitive-behavioral disorders that could affect the completion of self-questionnaires;\n* Local or systemic infection, or suspicion of infection;\n* Severe coagulation disorders;\n* Other inflammatory rheumatic disease;\n* Severe underlying pathology with life expectancy \\\u003C1 year;\n* Women of childbearing age who are pregnant at the inclusion visit or who wish to become pregnant before the administration of the treatment (V0);\n* Known allergy to contrast material and\u002For local anesthetic substances;\n* Patients who cannot read or write Italian;\n* Major person benefiting from a legal protection regime (guardianship, curatorship, safeguard of justice);","120 Years",{"count":49,"type":20},60,[51,52],"PHASE2","PHASE3","The purpose of this study is to assesse safety and efficacy of the Intradiscal Gelified Ethanol for treatment in refractory cervical discogenic pain.",[55,56],"Pain, Cervical","Discogenic Pain","NOT_YET_RECRUITING","2025-03-07",{"date":60,"type":31},"2025-03-11",{"date":62,"type":20},"2025-04",{"date":64,"type":20},"2026-04",{"name":37,"class":38},""]