[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100495923":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":37,"centralContacts":37,"locations":37,"responsibleParty":38,"collaborators":37,"id":42,"slug":43,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":37,"eligibilityCriteria":48,"healthyVolunteers":44,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":37,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":37,"overallStatus":61,"whyStopped":37,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":37},{"fullName":5,"class":6},"Sultan Qaboos University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Hydroxyzine","EXPERIMENTAL","Hydroxyzine (25 mg\u002Fday) for eight weeks, the dose of hydroxyzine may be adjusted based on tolerability and clinical judgment, max 100mg\u002Fday",[13],"Drug: Hydroxyzine",{"label":15,"type":16,"description":17,"interventionNames":18},"Treatment as Usual","ACTIVE_COMPARATOR","Treatment as usual includes the currently approved treatment according to CANMAT and Muadesly guidelines",[19],"Drug: Escitalopram Oxalate",[21,28],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Oral tablet of hydroxyzine 25mg at night which could be increased to TID or QID",[9],[26,27],"Atarax","Vistaril",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"Escitalopram Oxalate","The treatment as usual can include first-line, second-line and third-line recommendations",[15],[33,34,35,36],"citalopram","fluoxetine, fluvoxamine, paroxetine, paroxetine CR, sertraline, venlafaxine XR,","Alprazolam, clomipramine, clonazepam, diazepam, imipramine, lorazepam, mirtazapine, reboxetine","Bupropion SR, divalproex, duloxetine, gabapentin, levetiracetam, milnacipran, moclobemide, olanzapine, phenelzine, quetiapine, risperidone, tranylcypromine",null,{"type":39,"investigatorFullName":40,"investigatorTitle":41,"investigatorAffiliation":5,"oldNameTitle":37,"oldOrganization":37},"PRINCIPAL_INVESTIGATOR","Mohammed Al Alawi","Principal Investigator, Dr Mohmmed Al Alawi Bsc, MD,PhD, MRCPsych, OMSBPsych, ARABPsych","100495923","phase-4-efficacy-of-hydroxyzine-for-patients-with-panic-disorder-100495923",false,"NCT05737511","Efficacy of Hydroxyzine for Patients With Panic Disorder","Efficacy of Hydroxyzine Versus Treatment as Usual for Panic Disorder: An Eight-Week, Open Label, Pilot, Randomized Controlled Trial.","Inclusion Criteria:\n\n* The study will recruit adult patients (18 years and older)\n* Confirmed diagnosis of the panic disorder according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-5).\n* Participants will be included if they have had at least one panic attack per week for the last four weeks,\n* Have not received any pharmacological treatment for panic disorder in the past four weeks,\n* Willing to discontinue any current benzodiazepine or SSRI treatment for the duration of the study.\n\nExclusion criteria:\n\n* Current substance abuse or dependence,\n* Medical diseases\n* Psychiatric comorbidities,\n* Pregnancy or lactation.","ALL","19 Years","60 Years",{"count":53,"type":54},80,"ESTIMATED","INTERVENTIONAL",[57],"PHASE4","The aim of this study is to evaluate the efficacy of hydroxyzine compared to treatment as usual (TAU) for patients with panic disorder. By conducting a pilot study, we hope to provide initial data on the feasibility and potential impact of hydroxyzine for this population. This will inform the design and power calculations of a larger, more comprehensive study in the future.\n\nObjectives:\n\nTo assess the feasibility of conducting a randomized controlled trial (RCT) of hydroxyzine for panic disorder.\n\nTo evaluate the effectiveness of hydroxyzine compared to TAU in reducing panic symptoms in patients with panic disorder.\n\nTo explore the potential side effects and tolerability of hydroxyzine in this population.\n\nMethods:\n\nThis will be a single-center, open-label, randomized pilot study. A total of 30 patients with a primary diagnosis of panic disorder will be recruited from a psychiatric outpatient clinic. Participants will be randomly assigned to receive either hydroxyzine or TAU for 8 weeks. The primary outcome measure will be the change in panic symptoms as assessed by the Panic Disorder Severity Scale (PDSS). Secondary outcome measures will include the Hamilton Anxiety Rating Scale (HAM-A) and the Clinical Global Impression-Severity (CGI-S) scale. Participants will be assessed at baseline, 4 weeks, and 8 weeks. Adverse events will be monitored throughout the study.\n\nExpected Results:\n\nThis pilot study is expected to provide preliminary data on the feasibility and potential efficacy of hydroxyzine for panic disorder. The results will inform the design of a larger RCT to further evaluate the efficacy of hydroxyzine for this population.\n\nSignificance:\n\nThere is a need for effective and well-tolerated treatments for panic disorder. If found to be effective, hydroxyzine could provide a new option for patients with this condition, potentially improving their quality of life and functioning. The results of this pilot study will inform the design of future studies and contribute to the development of evidence-based treatments for panic disorder.",[60],"Panic Disorder","NOT_YET_RECRUITING","2023-02-20",{"date":64,"type":65},"2023-02-21","ACTUAL",{"date":67,"type":54},"2023-12-30",{"date":69,"type":54},"2026-12-30",{"name":5,"class":6}]