Clinical Trials on Safety Study for Future Treatment of Psoriasis
Total 209 results
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One World Cannabis Ltd.CompletedSafety Study for Future Treatment of PsoriasisIsrael
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Atatürk UniversityUnknownThis Study Will Provide Data Comparing Safety of LMWH Versus UFH in the Treatment of Acute PE Cases Who Require Thrombolytic Treatment.Turkey
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Michelle ColeTerminatedFocus of Study: The Safety of an Online Pre-assessment Tool
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University Hospital of PatrasNot yet recruitingStudy Focuses on the Use of Covered Stents (Stent Grafts) for the Treatment of Dysfunctional Vascular Access of Hemodialysis Patients
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University of PittsburghNational Center for Complementary and Integrative Health (NCCIH)CompletedPersons Receiving Any Medical or Behavioral Treatment (Focus of Study is Questionnaires)United States
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The Hillshire Brands CompanyBiofortis Clinical Research, Inc.Unknown
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NoNO Inc.RecruitingFirst-In-Human Study to Evaluate Safety of a New Drug Intended for Treatment of Acute Ischemic StrokeCanada
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University of CologneUnknownChildren With ADHD Symptoms >90th Percentile (FBB-ADHS-V); no Beginning or Completion of Psychotherapeutically or Psychopharmalogical Treatment During the StudyGermany
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Lee's Pharmaceutical LimitedFidia Farmaceutici s.p.a.CompletedThe Primary Objective of This Study Was to Assess the Efficacy and Safety of Hyaluronic Acid Vaginal Gel in Treating Vaginal Dryness
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Azitra Inc.RCTsCompletedStudy of Three Doses of AZT-04 for Skin AppearanceUnited States
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Albert Einstein College of MedicineRecruitingSafety and Efficacy of Radiation Therapy for the Treatment of KeloidsUnited States
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Universidad Católica San Antonio de MurciaUniversidad de AlmeriaActive, not recruitingAdults | No Sagittal Spine Disposition Disorder | No Surgery on the Spine or the Hamstring | No Specific Treatment for Spinal Pathology | Not Involved in Structured Exercise Programs Before or During the Time of the StudySpain
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Jinnah Sindh Medical UniversityAl Khidmat Hospital Nazimabad Karachi; Medics Laboratories (Pvt.) Ltd.CompletedThe Main Focus of This Study is to Evaluate the Safety of Zingiber Officinale L. Tablets as Hypolipidemic Agent in Hypertensive PatientsPakistan
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Heba A YassaEnrolling by invitationthe Study Focus on the Uses of Telephone and Other New Technology in Medicine, Diagnosis and TreatmentEgypt
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Novartis PharmaceuticalsCompletedPatients Successfully Completing the 12-month Treatment Period of the Core Study (de Novo Heart Recipients) Who Were Interested of Being Treated With EC-MPS
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Scripps Translational Science InstituteCompletedHypertension | Hypertension, Grade 1 | Hypertension Treatment | N of 1 Study DesignUnited States
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Jiangsu Nhwa Pharmaceutical Co., Ltd.CompletedEfficacy and Safety of Mivacurium Chloride for Pediatric Patients
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The HIV Netherlands Australia Thailand Research...National Health Security Office, Thailand; Ministry of Education, ThailandCompletedThis Study is Designed to Collect Treatment Data of Thai Children on Third Line ARV TherapyThailand
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Herlev HospitalCompletedFocus of Study: Usability of a Tool for Structured Assessment of and Feedback to Trainee SurgeonsDenmark
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AbbViePPDRecruitingPlaque Psoriasis | Crohn Disease | Psoriatic Arthritis | Other Conditions for Which Risankizumab is an FDA-approved TreatmentUnited States
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Ruhr University of BochumUnknownIn the Study the Value of Capnography for Avoiding Complications During Sedation for PEG is Evaluated.Germany
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University Hospital, GasthuisbergCompletedthe Focus of This Study is to Measure the Intra- and Interobserver Agreement for the Evaluation of Early Stage EmbryosBelgium
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Hecheng Li M.D., Ph.DSecond Affiliated Hospital, School of Medicine, Zhejiang University; Ruijin... and other collaboratorsRecruitingThe Safety of Ultrasound Knife Coagulation for Blood Vessels With a Diameter Greater Than 5mm and Less Than or Equal to 7mmChina
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Mid Michigan Health CentersCompletedNo Conditions for This Study. All Male Patients 18 Years of Age or Older Were Administered the LUTS, MSHQ, and Patient Demographics QuestionnaireUnited States
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Central Hospital, Nancy, FranceRecruitingStudy of Risk Factors for IPMNs Degeneration at the Nancy CHRUFrance
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University of AlbertaRecruitingValidation Study of Molecular Diagnostic System | Development of Reporting System for Molecular Diagnosis | Incorporate Molecular Diagnosis Into Diagnostic StandardsUnited States, Switzerland, Austria, Croatia, Slovenia, Canada, Czechia, France, Germany, Ireland, Korea, Republic of, Poland, Spain, United Kingdom
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Tanta UniversityRecruitingthe Efficacy of Ultrasound Guided Sacroiliac Injection of Ozone, Platelet Rich Plasma (PRP) or Steroid for Treatment of SacroiliitisEgypt
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Synergy Health Concepts, Inc.UnknownTo Determine the Safety and Validity of Venous Angioplasty and | Valvuloplasty in the Treatment of CCSVI. In Addition, it Will | Allow Researchers to Sub-classify Valve Morphology in Relation | to Treatment Success. This Will be Evidenced by Venous Patency | Forty-eight Hours by Doppler... and other conditionsUnited States
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BeiGeneCompletedFor Participants With Advanced Solid Tumors Failed With Previous Lines of TreatmentAustralia
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University Hospital, Gentofte, CopenhagenUniversity of CopenhagenUnknownThe Focus of This Study is to Evaluete the Significances of the Vagal Cholinerg Nervuos System for the Effect of GLP-1 by Using Atropin Administration.Denmark
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Shandong New Time Pharmaceutical Co., LTDCompletedA Phase IV Trial to Investigate the Efficacy and Safety of Huazhi Rougan Granule in the Treatment of Non-alcoholic Simple Fatty LiverChina
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AstraZenecaCompletedThe Aim of This Study is to Investigate the Frequency and Related Risk Factors of Recurrence, and Quality of Life in Patients With GERD After Treatment With PPIKorea, Republic of
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University Of PerugiaUnknownThe Primary Study Objective is to Assess the Efficacy and | Safety of Extended 4-week Heparin Prophylaxis Compared to | Prophylaxis Given for 8±2 Days After Planned Laparoscopic | Surgery for Colorectal Cancer. | The Clinical Benefit Will be Evaluated as the Difference in | the Incidence of... and other conditionsItaly
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Hadassah Medical OrganizationUnknownInterventional Study | Biological Therapy for Chronic Anal Fissure | Treatment by Biological Factors - Activated MacrophagesIsrael
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Peking UniversityRecruitingConditions or Focus of Study: B7-H3 Positive Relapsed/Advanced Malignant Solid TumorChina
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Shanghai Mental Health CenterRecruitingDeep Transcranial Magnetic Stimulation for the Treatment of Treatment Resistance SchizophreniaChina
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Bradford Teaching Hospitals NHS Foundation TrustUnknownBracket Failure Rate | Bonding Time Per Bracket | Adhesive Remnant Index for Type of Bond Failure | Length of Treatment | Peer Assessment Rating
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Chittagong Medical CollegeCompletedTo See the Safety and Efficacy of the Topical Latanoprost Compared With Topical Brimonidine in the Treatment of the Primary Open Angle Glaucoma PatientsBangladesh
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Hong Kong Baptist UniversityThe Hong Kong Jockey Club Charities TrustCompletedCross-cultural Adaptation, Evaluation and Validation Study of Wang Qi's Constitution in TCM Questionnaire (For Old Person)China
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Soroka University Medical CenterCompletedOptimization of Second Line Treatment Protocol for H Pylori EradicationIsrael
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Smith & Nephew, Inc.Medical Metrics Diagnostics, Inc; Global Research SolutionsTerminatedArthroscopic Surgical Treatment of High-grade (>50%) PartialthicknessUnited States
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Wuhan UniversityPeking University; PfizerUnknownThe Primary Evaluation is the Change From Baseline at End of Study for CDSS Total Scores. | The Secondary Efficacy Evaluations Include: MADRS, PANSS Total Scores and Subscales and Responder Rate; CGI-S and CGI-I Scales. | Safety Evaluations Include: Laboratory Test Abnormalities; BARS... and other conditions
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University of LiegeUnknownComparison of Treatment for Chronic Non-malignant and Malignant PainBelgium
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Ology BioservicesCompletedPhase 1 Safety Study of GelVac Nasal Powder H5N1 Influenza VaccineUnited States
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University of Sao PauloSantanderTerminatedEar Acupuncture Effectiveness In Reducing The Signs And Symptoms Of Stress And Anxiety (EAEIRTSOSAA)Inclusion Criteria: | Voluntary Participation in the Study With Available Time for Submission to the Sessions, Which Occur Over Two Months. | Have a Score of Stress Medium, High or Very High in the LSS Questionnaire, Completion of the STAI and General Form. | Exclusion Criteria: | Pregnant...
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Novartis PharmaceuticalsUniversity of PennsylvaniaRecruitingLong Term Safety of Patients Receiving CAR-T in an Eligible Clinical Trial or Managed Access ProgramUnited States, Japan, Australia, Germany, Spain, Belgium, Taiwan, Italy, Canada, Israel, Singapore, United Kingdom, Denmark, Finland, Norway, Austria, Netherlands, France
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FX SolutionsRecruitingShoulder Fractures | Shoulder Disease | Shoulder Arthroplasty for Revision of Previous TreatmentMonaco, France
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Cairo UniversityUnknownTo Assess Bucco-lingual Dimension of the Ridge While Using Pontic Shield Technique as a Treatment Modality for Ridge PreservationEgypt
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Shanghai Children's Medical CenterNot yet recruitingTo Analyze and Compare the Efficacy and Safety of Ondansetron and Tablet for the Prevention of Moderate and Hypoemetic Chemotherapy
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University of PennsylvaniaCompletedWomen Admitted to Labor and Delivery for the Management of Preterm Labor and/or Preterm Premature Rupture of Membranes (PPROM)United States