Molnlycke Health Care AB: all 59 studies

Page 1 of 1. Open to participants first (8), then studies with results posted, then the rest; newest registration first within each.

• Interventional Study to Describe the Utilization of Foam Dressings in Routine Clinical Practice, for the Treatment of Patients With Chronic Wounds in a Primary Healthcare Center in Italy.RecruitingNCT07926386Not applicable
• Performance and Safety of Mepilex® Up in Leg and Foot Ulcers and Skin TearsNot yet recruitingNCT07782008Not applicable
• A Randomized Non-Inferiority Study of Mepi™ Press 2 vs UrgoK2® for Compression Therapy in Venous Leg UlcersNot yet recruitingNCT07600489Not applicable
• An Investigation to Evaluate Wearing Properties of Three Different Investigational DevicesRecruitingNCT07034014Not applicable
• Evaluation of Adhesion Properties in Wound Care DevicesNot yet recruitingNCT06392165Not applicable
• Mepilex Border Flex Utilization Pilot SpainRecruitingNCT06321978
• A Clinical Investigation to Follow the Progress of Exuding Chronic Venous Leg Ulcers Using a Non-Bordered Foam DressingRecruitingNCT05608317Not applicable
• A Clinical Investigation to Follow the Progress of Exuding Chronic Wounds Using Mepilex® Up as the Primary Dressing.RecruitingNCT05588583Not applicable
• A Multicentre European Study to Evaluate Granulox® Used in the Treatment Pathway of Predominantly Chronic Venous Leg Ulcers (VLUs).TerminatedNCT04181320Not applicableResults posted
• A Clinical Investigation With Epaderm® CreamCompletedNCT03738163Not applicableResults posted
• Clinical Study to Compare 3 Multi-Layered Foam Dressings for the Management of Chronic WoundsCompletedNCT03662997Not applicableResults posted
• Evaluation of Exufiber Ag+ and Other Gelling Fibre DressingsCompletedNCT03249909Not applicableResults posted
• Self-adherent Absorbent Silver Dressing in Adults After Hip or Knee ArthroplastyCompletedNCT03016078Not applicableResults posted
• Pressure Injury Prevention in the ICU With Multi-Layer Foam DressingsCompletedNCT02962882Not applicableResults posted
• Investigation to Evaluate the Efficacy and Safety of Exufiber Versus Aquacel Extra in Moderately or Strongly Exuding Venous and Mixed Ulcers of Predominantly Venous OriginCompletedNCT02921750Not applicableResults posted
• Clinical Investigation of Two Different Wound DressingsTerminatedNCT02904200Not applicableResults posted
• Prospective, Randomized Clinical Investigation of Two Different Postoperative Wound DressingsCompletedNCT02653183Not applicableResults posted
• A Prospective, Open, Non-controlled Clinical Investigation to Evaluate the Performance and Safety of an Antimicrobial Foam Transferring Dressing in Patients With Malignant WoundsCompletedNCT02431741Not applicableResults posted
• Prospective, Randomized, Non-inferiority Investigation to Compare Effects of Mepitel® One and UrgoTul® Dressings in Acute Wound Management (Only)"CompletedNCT02237118Not applicableResults posted
• Post Market Clinical Follow-up Investigation to Evaluate Performance and Safety on Pressure Ulcers, PU, When Using Exufiber as IntendedCompletedNCT02224404Not applicableResults posted
• A Soft Silicone Wound Contact Layer Containing Silver in the Treatment of Skin Grafts in Surgical Burn Patients.CompletedNCT02210208Not applicableResults posted
• A Multicenter, Post Marketing Clinical Follow up (PMCF) Investigation to Evaluate the Performance and Safety of a Soft Silicone Foam Dressing and to Evaluate the Performance of Standard Care in Exuding Venous Leg UlcersCompletedNCT02167815Not applicableResults posted
• Open, Non-comparative, Multi-centre Post Marketing Clinical Follow-up Investigation to Evaluate Performance and Safety on Diabetic Foot Ulcer, DFU When Using Fast Gelling Dressing as Intended.CompletedNCT02091778Not applicableResults posted
• Evaluation of Core Body Temperature When Using Forced Air Warming or an Active Blanket to Prevent Perioperative HypothermiaCompletedNCT02079311Not applicableResults posted
• Post Market Clinical Follow Up Study of Avance Foam Abdominal Dressing Kit in Open AbdomenCompletedNCT01968811Not applicableResults posted
• Proof of Concept (Design Validation) in Patient With Hard to Heal Wounds Such as Pressure Ulcer, Diabetic Foot Ulcer and Leg Ulcer, LeiaTerminatedNCT01966380Phase 2Results posted
• TITLE: An Open, Non-comparative, Multi-centre Post Marketing Clinical Follow-up (PMCF) Investigation to Evaluate Performance and Safety on Diabetic Foot Ulcer, DFU, When Using Mepilex Transfer Ag as IntendedCompletedNCT01964521Not applicableResults posted
• Study to Evaluate Safety and Efficacy of Blanket Used to Prevent Anesthesia Induced HypothermiaCompletedNCT01900067Not applicableResults posted
• Post Market Clinical Follow-up StudyCompletedNCT01841567Phase 4Results posted
• An Open Single-centre Investigation Evaluating Efficacy in Second Degree Partial Thickness Burns Using a Silicone Contact Layer Containing Silver.CompletedNCT01734317Not applicableResults posted
• An Investigation to Evaluate a New Donor Site Dressing in Surgical Burn PatientsCompletedNCT01670201Not applicableResults posted
• A Clinical Investigation to Evaluate Efficacy of Mepitel Ag in Partial Thickness Second Degree BurnsCompletedNCT01636362Not applicableResults posted
• Clinical Utility of a New Silver Gel for Use on Chronic WoundsCompletedNCT01442103Not applicableResults posted
• Mepilex Ag Versus Silver Sulfadiazine in Children and Adults With Burn Injuries.CompletedNCT01439074Not applicableResults posted
• A Multi-centre Evaluation of the Performance of Window Dressings on Subjects With High Risk Pressure UlcerationCompletedNCT01438541Phase 4Results posted
• Evaluation of Antimicrobial Soft Silicone, Silver Containing, Foam Dressing, Mepilex Border Ag, in Second Degree BurnsCompletedNCT01418482Not applicableResults posted
• Open, Prosp, Rand. Invest. Evaluating Pain With Mepitel One vs.Bridal Veil and Staples on Split Thickness Skin GraftsCompletedNCT01365273Phase 4Results posted
• A Open Study to Evaluate the Performance of Dressing on Subject With High Risk of Skin BreakdownCompletedNCT01354899Results posted
• Open Multi-centre Investigation to Evaluate Signs and Symptoms of Local Inflammation/Infection on Chronic Ulcers and Partial Thickness Burns When Using Mepilex Border Ag as an Anti-microbial Wound DressingCompletedNCT01214811Phase 3Results posted
• Evaluating the Efficacy of an Absorbent Foam Dressing Containing Silver (Mepilex Ag) Versus the Same Dressing Without Silver Used on Subjects With Venous Leg Ulcers or Mixed UlcersCompletedNCT01036438Phase 4Results posted
• Evaluation of Negative Pressure Wound Therapy in the Treatment of DFUs Incl. Post Amputation Wounds.CompletedNCT01011387Not applicableResults posted
• Evaluating the Cost-effectiveness, Efficacy, Safety and Tolerance of Mepilex® Ag Versus Silvadene®CompletedNCT00742183Not applicableResults posted
• Interventional Study Exploring the Occurrence of Surgical Site Infections.CompletedNCT06661473Not applicable
• An Open, Non-comparative, Multicenter Investigation to Evaluate the Safety and Performance of Exufiber Ag+, a Gelling Fiber Silver Dressing, When Used in Medium to High Exuding Chronic WoundsTerminatedNCT05494450Not applicable
• A Post-Market Clinical Investigation on Mepilex Border Post-OpStatus unknownNCT04994145
• A PMCF Investigation on Exuding Chronic Wounds Using Exufiber® as Primary Dressing, and Mepilex® Border Flex/ComfortTerminatedNCT04960553Not applicable
• A 96-hour Patch Test Study Using Healthy Human Volunteers to Assess the Skin Irritation Potential of 11 Topically Applied FormulationsStatus unknownNCT04942496Phase 4
• A Safety and Performance PMCF Investigation of the Avance® Solo NPWT System in Surgically Closed IncisionsStatus unknownNCT04894604Not applicable
• Confirm Performance and Safety of Exufiber When Used as Intended on Donor SitesCompletedNCT04884568Not applicable
• Performance and Safety of Exufiber Ag+ and Exufiber on Partial Thickness BurnsActive, not recruitingNCT04839523Not applicable
• A Clinical Investigation With BARRIER® EasyWarm®CompletedNCT04813809Not applicable
• Confirm the Safety and Performance of Avance Solo NPWT SystemCompletedNCT04754048Not applicable
• Confirm Safety and Performance of Avance Solo and Avance Solo Adapt NPWT SystemsCompletedNCT04753294Not applicable
• Evaluation of the Residual Antimicrobial Efficacy of One Test Material Based on a Modification of ASTM E1115-11 Test MethodCompletedNCT04654182Phase 4
• Evaluation of Chlorhexidine Gluconate Concentration on Skin of Human Subjects Following Multiple Application TimesCompletedNCT04235985Phase 4
• Durability of Double-gloving With Biogel® Surgical Gloves When Used by Clinicians/SurgeonsCompletedNCT03344354Not applicable
• An Investigation to Evaluate the Function of a New Silicon Cover Film and an On-top Suction Device to be Used in a NPWT System in the Treatment of Acute and Chronic WoundsCompletedNCT01286857Phase 2/3
• A Prospective, Open, Non-controlled Clinical Investigation to Evaluate a New Negative Pressure Wound Therapy (NPWT) System to be Used in the Treatment of Acute Non-infected Wounds and Post Surgical Infected WoundsCompletedNCT01195896Not applicable
• Investigation Evaluating Handling of Mepitel® One Used in Acute Wounds in Home CareWithdrawnNCT01164982Not applicable

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