[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613251":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":44,"responsibleParty":60,"collaborators":26,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":26,"eligibilityCriteria":69,"healthyVolunteers":65,"sex":70,"minAge":71,"maxAge":72,"enrollmentInfo":73,"targetDuration":26,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":47,"whyStopped":26,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Uşak University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Laser Therapy Group (LTG)","EXPERIMENTAL","The treatment protocol comprised two distinct modes: the first being the administration of analgesic medication, and the second being biostimulation. For the analgesic mode, the laser was administered at an operating power of 10W, with the energy density set at 12J\u002Fcm2 across a surface area of 15cm2. The laser will applied in along the right and left sacroiliac joints for four minutes. The total energy delivered will 600 J. In the biostimulation mode, a laser with an operating power of 5 W will applied, generating an energy density of 120 J\u002Fcm2 across a surface area of 15 cm2 at the sacroiliac joint line for a duration of 10 minutes, resulting in a total energy output of 3,000 J.\n\nApplication Technique: The applicator will be moved in a slow, circular, or grid pattern over the target area for 12 minutes.",[13,14],"Device: Laser Therapy","Other: Exercises for both groups",{"label":16,"type":17,"description":18,"interventionNames":19},"Sham Therapy Group (STG)","SHAM_COMPARATOR","Protocol and dosage: In all aspects, including the device's appearance, audible cues (e.g. timer beeps), treatment duration and the physical application of the probe to the skin, the sham protocol will be identical to the active protocol.",[14],[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Laser Therapy","Protocol and dosage: Treatment will be applied directly over the painful sacroiliac joint(s). The treatment protocol comprised two distinct modes: the first being the administration of analgesic medication, and the second being biostimulation. For the analgesic mode, the laser was administered at an operating power of 10W, with the energy density set at 12J\u002Fcm2 across a surface area of 15cm2. The laser will applied in along the right and left sacroiliac joints for four minutes. The total energy delivered will 600 J. In the biostimulation mode, a laser with an operating power of 5 W will applied, generating an energy density of 120 J\u002Fcm2 across a surface area of 15 cm2 at the sacroiliac joint line for a duration of 10 minutes, resulting in a total energy output of 3,000 J.\n\nApplication Technique: The applicator will be moved in a slow, circular, or grid pattern over the target area for 12 minutes.",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Exercises for both groups","Participants will be taught the supervised exercise programme. Sessions will be held three times per week on non-consecutive days. Each session will last approximately 45 minutes.\n\nThe exercise programme was designed to address pain and dysfunction related to hypomobility and instability of the sacroiliac joint (SIJ). The intervention comprises a structured, progressive exercise regimen consisting of three sequential phases: 1) Gentle Movement and Relaxation, 2) Specific Self-Mobilisation and 3) Core and Stabilisation. The protocol will be delivered to participants in a standardised format, with progression based on individual tolerance and clinical milestones.",[9,16],[32],{"name":33,"affiliation":5,"role":34},"Ali Y Karahan, Professor","PRINCIPAL_INVESTIGATOR",[36,40],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","+905386921934","ali.karahan@usak.edu.tr",{"name":41,"role":37,"phone":42,"phoneExt":26,"email":43},"Kagan Ozkuk, Professor","+905055601815","kagan.ozkuk@usak.edu.tr",[45],{"facility":46,"status":47,"city":48,"state":26,"zip":49,"country":50,"countryCode":26,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"University of Usak","RECRUITING","Uşak","64200","Turkey (Türkiye)",{"type":52,"coordinates":53},"Point",[54,55],29.4058,38.67351,{"lat":55,"lon":54},[58],{"name":59,"role":37,"phone":38,"phoneExt":26,"email":39},"Ali Y Karahan",{"type":34,"investigatorFullName":61,"investigatorTitle":62,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Ali Yavuz Karahan","Professor","100613251","laser-therapy-in-the-isotretinoin-induced-sacroiliitis-100613251",false,"NCT07264153","Laser Therapy in the Isotretinoin-Induced Sacroiliitis","Efficacy of High-Intensity Laser Therapy (HILT) in the Management of Isotretinoin-Induced Sacroiliitis: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged between 18 and 35 years.\n* Receiving a stable dose of oral isotretinoin (e.g., 0.3-0.5 mg\u002Fkg\u002Fday) for at least one month.\n* Diagnosis of sacroiliitis based on: Clinical symptoms: Persistent (≥4 weeks) lower back\u002Fbuttock pain, morning stiffness \\>30 minutes, improvement with exercise. Positive physical findings: At least two positive sacroiliac joint provocation tests (e.g., FABER\u002FPatrick's test, Gaenslen's test, Compression\u002FDistraction test). Radiological confirmation (MRI): Active inflammation (bone marrow edema) on Short-Tau Inversion Recovery (STIR) sequences in one or both sacroiliac joints.\n* A baseline pain intensity of ≥4 on the Visual Analog Scale (VAS 0-10 cm).\n\nExclusion Criteria:\n\n* ankylosing spondylitis or other seronegative spondyloarthritis\n* the presence of pregnancy\n* the presence of any cancer\n* the presence of multiple sclerosis","ALL","18 Years","35 Years",{"count":74,"type":75},50,"ESTIMATED","INTERVENTIONAL",[78],"NA","The clinical significance of this adverse effect lies in its impact on quality of life and the potential for misdiagnosis. The symptomatology can be severe enough to limit daily activities and may be mistakenly attributed to a primary rheumatic disease, leading to unnecessary long-term immunosuppressive therapy if the temporal link to isotretinoin is not identified. Therefore, a high index of suspicion is crucial for dermatologists, rheumatologists, and primary care physicians alike.\n\nAim: To compare the effectiveness of High-Intensity Laser Therapy (HILT) in reducing pain intensity, in patients diagnosed with Isotretinoin-Induced Sacroiliitis.",[81],"Sacroilitis",[23,83,84,85],"Isotretinoin","Sacroiliitis","Pain","2025-12-04",{"date":88,"type":89},"2025-12-12","ACTUAL",{"date":91,"type":89},"2025-11-24",{"date":93,"type":75},"2026-05-11",{"name":5,"class":6},1]