Merz Pharma: all 172 studies
Page 1 of 2. Open to participants first (3), then studies with results posted, then the rest; newest registration first within each.
- A Study to Confirm Safety and Effectiveness of RADIESSE® Injectable Implant for the Correction of Moderate to Severe Nasolabial FoldsNot yet recruitingNCT07856797Not applicable
- Real-world Patient Experiences With Inbrija®RecruitingNCT07797790
- Effectiveness and Safety of the Ulthera® System for Skin Laxity in the Lower Face, Submentum and NeckRecruitingNCT07614997Not applicable
- Prospective Study to Assess Tissue Responses After Injection With Biostimulatory ProductsCompletedNCT06093815Not applicableResults posted
- A Study of Belotero® Intense Lidocaine for Lip AugmentationCompletedNCT05773066Not applicableResults posted
- Evaluation of the Effectiveness and Safety of Diluted RADIESSE® in the Treatment of Décolleté WrinklesCompletedNCT05163353Not applicableResults posted
- Effectiveness and Safety of the Octave System for Lifting the Eyebrow and Improving the Appearance of the Face and NeckCompletedNCT05067504Not applicableResults posted
- Evaluation of the Effectiveness and Safety of the Ulthera® DeepSEE® System for Treating Skin Laxity in the Lower Face and SubmentumCompletedNCT04795622Not applicableResults posted
- A Study to Investigate the Efficacy and Safety of NT 201 (Botulinum Toxin) Compared With Placebo for the Treatment of Adult Participants With Essential Tremor in the ArmCompletedNCT04766723Phase 2Results posted
- A Study of Octave System for Improving Lines and Wrinkles of the DécolletéCompletedNCT04681352Not applicableResults posted
- Evaluation of the Effectiveness and Safety of Radiesse for the Correction of Moderate to Severe Nasolabial FoldsCompletedNCT04647721Not applicableResults posted
- Safety and Efficacy Study of the Simultaneous Treatment of Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines and Crows Feet) in Subjects With Moderate to Severe Upper Facial LinesCompletedNCT04622254Phase 3Results posted
- Evaluation of Effectiveness and Safety of Belotero Balance® (+) Lidocaine for Volume Augmentation of the Infraorbital HollowCompletedNCT04594239Not applicableResults posted
- Safety and Efficacy Study of the Simultaneous Treatment of Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines and Lateral Canthal Lines) in Subjects With Moderate to Severe Upper Facial LinesCompletedNCT04594213Phase 3Results posted
- Investigation of the Effectiveness and Safety of MRZF111 in the Treatment of Décolleté WrinklesCompletedNCT04177212Not applicableResults posted
- Study to Investigate the Safety and Duration of Effect of Different Botulinum Toxin A (NT 201) Dose Groups Following the Treatment of Glabellar Frown LinesCompletedNCT03806933Phase 2Results posted
- A Pilot Study to Assess the Effectiveness and Safety of Belotero Balance® Injection for Volume Augmentation of the Infraorbital HollowCompletedNCT03777917Not applicableResults posted
- Safety, Effectiveness and Participant Satisfaction Study of a Dermal Filler (of RADIESSE® (+) Lidocaine) in the Treatment of Ageing Signs in the FaceCompletedNCT03650387Not applicableResults posted
- Evaluation of the Ulthera® System and Efficacy Correlation to Morphological DifferencesCompletedNCT03599349Not applicableResults posted
- Evaluation of Effectiveness and Safety of Radiesse (+) to Improve the Contour of Jawline by Adding Volume to the JawlineCompletedNCT03583359Not applicableResults posted
- Clinical Study on the Application of a Non-Invasive Micro-Focused Ultrasound With Visualization System for Skin Laxity (ULT-215)CompletedNCT03545412Not applicableResults posted
- Open-label, Prospective Evaluation of the Ulthera® System for Lifting Submental (Under the Chin) and Neck Tissue in Chinese PatientsCompletedNCT03351335Not applicableResults posted
- Evaluation of the Ulthera System for Treating Axillary HyperhidrosisCompletedNCT03320096Not applicableResults posted
- Evaluation of Pain With Belotero® Balance With Integral Lidocaine for Correction of the Nasolabial FoldsCompletedNCT03319719Not applicableResults posted
- Evaluation of the Effectiveness and Safety of Radiesse for the Correction of Nasolabial Folds in ChinaCompletedNCT03282357Not applicableResults posted
- Radiological Evaluation of Radiesse Implantation in the HandsCompletedNCT02949921Not applicableResults posted
- Radiesse® Safety Study For the Treatment of HandsCompletedNCT02904096Not applicableResults posted
- Evaluation of the MJGS Following Radiesse (+) Injection Into the JawlineCompletedNCT02904057Not applicableResults posted
- Simulines Non-Inferiority Pivotal StudyTerminatedNCT02736825Not applicableResults posted
- Gene Expression Following Ultherapy® TreatmentTerminatedNCT02441036Not applicableResults posted
- Clinical Study to Investigate the Efficacy and Safety of NT 201 Compared to Placebo in the Treatment of Chronic Troublesome Drooling Associated With Neurological Disorders and/or Intellectual DisabilityCompletedNCT02270736Phase 3Results posted
- Botulinum Toxin A to Treat Arm TremorCompletedNCT02207946Phase 2Results posted
- The Treatment of Glabellar Frown LinesCompletedNCT02096081Phase 4Results posted
- Clinical Study to Investigate the Efficacy and Safety of Two Dose Levels of NT 201 Versus Placebo in Treating Chronic Troublesome Sialorrhea in Various Neurological ConditionsCompletedNCT02091739Phase 3Results posted
- Dose-response Study of Efficacy and Safety of Botulinum Toxin Type A to Treat Spasticity of the Arm(s) or of Arm(s) and Leg(s) in Cerebral PalsyCompletedNCT02002884Phase 3Results posted
- Long-term Open-label Study of Botulinumtoxin Type A to Treat Spasticity of Leg(s) or Leg(s) and Arm in Cerebral PalsyCompletedNCT01905683Phase 3Results posted
- Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Abnormal Contraction or Twitch of the EyelidCompletedNCT01896895Phase 3Results posted
- Dose-response Study of Efficacy and Safety of Botulinum Toxin Type A to Treat Spasticity of the Leg(s) in Cerebral PalsyCompletedNCT01893411Phase 3Results posted
- Evaluation of Radiesse® Dermal Filler for Hand TreatmentCompletedNCT01832090Not applicableResults posted
- Treatment of the Face and Neck With Lower Ulthera System Energy SettingsCompletedNCT01713998Not applicableResults posted
- Evaluation of the Ulthera® System for Treatment of the BrachiaCompletedNCT01713933Not applicableResults posted
- Evaluation of the Ulthera System for the Treatment of the DecolletageCompletedNCT01713686Not applicableResults posted
- Pharmacokinetic Study of Pediatric Subjects With Tinea Cruris and Tinea PedisCompletedNCT01712360Phase 4Results posted
- Feasibility Study: Heavy Water Tissue Labeling ProtocolCompletedNCT01708525Not applicableResults posted
- Study of the Cabochon System for Improvement in the Appearance of CelluliteCompletedNCT01671839Not applicableResults posted
- Belotero Post Approval StudyCompletedNCT01635855Phase 4Results posted
- Efficacy and Safety Dose Titration Study of Botulinum Toxin Type A to Treat Spasticity in the Leg and ArmCompletedNCT01603459Phase 3Results posted
- A Retrospective Study to Evaluate the Effectiveness of the Ulthera SystemCompletedNCT01519934Results posted
- Lifting and Tightening of the Face and Neck Following an Increased Density TreatmentCompletedNCT01519206Not applicableResults posted
- Open-Label Non-Inferiority Study Evaluating the Efficacy and Safety of Xeomin® in Subjects With Cervical Dystonia FlexCompletedNCT01486264Phase 4Results posted
- Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a StrokeCompletedNCT01464307Phase 3Results posted
- Ultherapy™ Treatment Following Sculptra® TreatmentCompletedNCT01422538Not applicableResults posted
- Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Arm After a StrokeCompletedNCT01392300Phase 3Results posted
- Lifting and Tightening of the Face in Subjects With Skin of Darker ColorCompletedNCT01368965Not applicableResults posted
- Reducing Wrinkles Around the Eyes Using the Ulthera® SystemCompletedNCT01368900Not applicableResults posted
- Lifting and Tightening of the Face and Neck Utilizing the Ulthera® SystemCompletedNCT01368874Not applicableResults posted
- Evaluation of the Ulthera™ System for Obtaining Lift and Tightening of the Cheek TissueCompletedNCT01368835Not applicableResults posted
- Evaluation of the Efficacy and Safety of NAFT-600 in Subjects With Tinea PedisCompletedNCT01290341Phase 3Results posted
- Efficacy and Safety of NAFT-600 in Subjects With Tinea PedisCompletedNCT01289015Phase 3Results posted
- Evaluation of Pain With Radiesse® With Lidocaine for Nasolabial FoldsCompletedNCT01069354Not applicableResults posted
- Evaluation of Pain With Lidocaine-Mixed Radiesse® Injectable Dermal FillerCompletedNCT01012661Phase 4Results posted
- Radiesse® Injectable Dermal Filler for the Treatment of Nasolabial Folds in Persons of ColorCompletedNCT01012388Phase 4Results posted
- Evaluation of Radiesse® Dermal Filler for Hand RejuvenationCompletedNCT01004107Not applicableResults posted
- This is a Post Approval Study of Coaptite® in the Treatment of Female Urinary IncontinenceCompletedNCT00996489Not applicableResults posted
- Safety and Effectiveness of Belotero® in Subjects With Fitzpatrick Phototypes IV Through VICompletedNCT00922623Not applicableResults posted
- Multicenter Study of the Safety and Effectiveness of Dermal Filler, Belotero®.CompletedNCT00876265Phase 3Results posted
- NT 201 (Xeomin®/Bocouture®) in Comparison With Clostridium Botulinum Toxin Type A in the Treatment of Glabellar Frown LinesCompletedNCT00777803Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Glabellar Frown LinesCompletedNCT00770211Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Glabellar Frown Lines No. 2CompletedNCT00770029Phase 3Results posted
- Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea CrurisCompletedNCT00750152Phase 3Results posted
- Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea PedisCompletedNCT00750139Phase 3Results posted
- Memantine and Antipsychotics UseTerminatedNCT00649220Phase 4Results posted
- Safety and Efficacy of NT 201 (IncobotulinumtoxinA [Xeomin]) in the Treatment of Glabellar Frown LinesCompletedNCT00512135Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) for Upper Limb SpasticityCompletedNCT00465738Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Post-stroke Spasticity of the Upper LimbCompletedNCT00432666Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Cervical DystoniaCompletedNCT00407030Phase 3Results posted
- IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of BlepharospasmCompletedNCT00406367Phase 3Results posted
- A Study of NT 201 in Adults With Moderate to Severe Platysma Prominence in Europe (PLATINUM EU)Active, not recruitingNCT07210463Phase 3
- A Study of NT 201 in Adults With Moderate to Severe Platysma Prominence in the United StatesActive, not recruitingNCT07122193Phase 3
- A Study to Determine if RADIESSE® Dilute Treatment in Décolleté of Adult Women Affects Radiographic Imaging AssessmentsActive, not recruitingNCT07086248Not applicable
- A Clinical Trial to Evaluate Efficacy and Safety of Xeomin® Injections for Preventing Chronic MigraineActive, not recruitingNCT07018713Phase 3
- A Clinical Trial to Evaluate Efficacy and Safety of Xeomin® Injections for Preventing Episodic MigraineActive, not recruitingNCT07018700Phase 3
- Validity and Inter-rater Reliability for Early Recognition of Spasticity Using the Decision Tree ToolCompletedNCT06381999
- A Clinical Trial to Investigate Efficacy and Safety of NT 201 Injections Compared With Placebo Injections in Participants Aged 18 Years and Older With Chronic Nerve Pain After Shingles or Nerve InjuryCompletedNCT06091020Phase 2
- Efficacy and Tolerability of Pantovigar® Vegan in Female Subjects With Diffuse Hair LossCompletedNCT05943860Not applicable
- Assessment of Long-term Clinical Response to BoNT in Cervical DystoniaCompletedNCT05884528
- A Study of NT 201 in the Treatment of Enlarged Pores and Excessive Sebum Production in the FaceCompletedNCT05784363Phase 1
- A Study of NT 201 Doses in the Treatment of Platysma ProminenceCompletedNCT05773053Phase 2
- A Study to Evaluate the Distribution of Botulinum Neurotoxin Type A Administered as Intradermal Injections, Comparing Different Doses, Concentrations, and Delivery MethodsCompletedNCT05585398Phase 1
- Longitudinal Evaluation and Real-world Evidence of NT201TerminatedNCT05222607
- A Prospective, Multicenter, Randomized, Comparator-controlled, Evaluator-blinded Study to Evaluate the Safety and Effectiveness of VP1 Lido US for Volume Augmentation of the CheekCompletedNCT04886232Not applicable
- Post-Market Clinical Follow-up Performance and Safety Study of Etermis 3 and 4 in the FaceCompletedNCT04210258
- Study to Compare the Efficacy and Safety of NT 201 (Botulinum Toxin) With Placebo for the Treatment of Lower Limb Spasticity Caused by Stroke or Traumatic Brain InjuryActive, not recruitingNCT03992404Phase 3
- Local Study of Akatinol Memantine in VaD in RussiaCompletedNCT03986424Phase 3
- Evaluation of the Merz Cheek Fullness Assessment Scale in the Treatment of Midface Volume DeficitCompletedNCT03321825Not applicable
- Evaluation of the Sensitivity of Merz Lips Fullness Assessment Scale Following Etermis 4® Treatment for Lips Volume AugmentationCompletedNCT03256942Not applicable
- Efficacy and Safety Study of MSRD-100 in Subjects With Atopic Dermatitis >=3 Months of Age and OlderWithdrawnNCT02677636Phase 3
- Efficacy and Safety Study of MSRD-100 in Subjects With Atopic Dermatitis >=3 Months of Age and OlderWithdrawnNCT02677610Phase 3
- Safety and Efficacy of NAFT900 in Children With Tinea CapitisWithdrawnNCT02658292Phase 2
- Neurogenic Dysphonia/Dysphagia RegistryTerminatedNCT02493491