Merz Pharma: Cutis Laxa trials
The registry lists 30 Cutis Laxa studies with Merz Pharma as lead sponsor. 1 are open to participants now and 14 have results posted.
No phase 30(a study in two phases counts in both)
Studies
Open to participants first, then studies with results posted, then the rest; newest registration first within each.
- Effectiveness and Safety of the Ulthera® System for Skin Laxity in the Lower Face, Submentum and NeckRecruitingNCT07614997Not applicable
- Evaluation of the Effectiveness and Safety of the Ulthera® DeepSEE® System for Treating Skin Laxity in the Lower Face and SubmentumCompletedNCT04795622Not applicableResults posted
- Evaluation of the Ulthera® System and Efficacy Correlation to Morphological DifferencesCompletedNCT03599349Not 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
- Simulines Non-Inferiority Pivotal StudyTerminatedNCT02736825Not applicableResults posted
- Gene Expression Following Ultherapy® TreatmentTerminatedNCT02441036Not applicableResults posted
- Treatment of the Face and Neck With Lower Ulthera System Energy SettingsCompletedNCT01713998Not applicableResults posted
- Feasibility Study: Heavy Water Tissue Labeling ProtocolCompletedNCT01708525Not applicableResults 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
- Ultherapy™ Treatment Following Sculptra® TreatmentCompletedNCT01422538Not applicableResults posted
- Lifting and Tightening of the Face in Subjects With Skin of Darker ColorCompletedNCT01368965Not 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
- Retrospective Evaluation of Combination Treatment With the Ulthera SystemCompletedNCT02444169
- Ultherapy® for Treating the Face and Neck Using Standard Versus Simulines TransducersCompletedNCT02416076Not applicable
- Feasibility Study: Evaluation of Ulthera Versus Thermage for Treating the Face and NeckCompletedNCT01713985Not applicable
- Evaluation of the Ulthera® System for Treatment of the Face and NeckTerminatedNCT01713907Not applicable
- Feasibility Study: Histological Characterization After Treatment With the Ulthera® SystemTerminatedNCT01713569Not applicable
- Feasibility Study: Lifting and Tightening Neck Skin in PatientsCompletedNCT01708928Not applicable
- Feasibility Study: Higher Density Ulthera® System Treatment With Vectoring for Treatment of the Face and NeckCompletedNCT01708512Not applicable
- Feasibility Study: Evaluation of the Ulthera® System for Treatment of Abdominal TissueCompletedNCT01708499Not applicable
- Feasibility Study: Compare the Effectiveness Between Two Pain Medications When Used Prior to Ultherapy™ TreatmentsCompletedNCT01708473Not applicable
- Feasibility Study: Ulthera Treatment of the Buttocks and ThighsCompletedNCT01708460Not applicable
- Feasibility Study: Evaluate the Effectiveness of Using a Topical Anesthetic Prior to Ultherapy™ TreatmentCompletedNCT01708447Not applicable
- Feasibility Study: Evaluation of the Ulthera® System for Treatment of the KneesCompletedNCT01708434Not applicable
- Feasibility Study: Lifting and Tightening of the ElbowsCompletedNCT01708382Not applicable
- Feasibility Study: Treatment of Post-surgery and Surgery Naive Patients Who Failed to Respond to a Previous Ulthera TreatmentCompletedNCT01708252Not applicable
- Feasibility Study: Evaluation of the Ulthera® System for Treatment of the DécolletéCompletedNCT01485107Not applicable