Our grouping. This page groups the registry's lead sponsor names by company — our grouping, not the registry's. It can be wrong or incomplete: an acquired company whose name never mentions its owner may be missing. Use “Something wrong?” under any name below to correct it.
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Coloplast A/S clinical trials
The registry lists 181 studies whose lead sponsor is Coloplast A/S or one of 4 companies grouped under it. 14 are recruiting or about to start. Per ClinicalTrials.gov, last updated Oct 20, 2026.
Keep track of what changes. Save the Coloplast A/S studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesRegistry sponsor names on this page
Each name exactly as ClinicalTrials.gov lists it, and how it relates to Coloplast A/S.
- Coloplast A/S150 studiesSame company
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- 14 studies →
- 13 studies →
- Laboratoires Coloplast S.A.S2 studies →Regional office
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- Nine Continents Medical, Inc.1 study →Acquired — became part of Coloplast A/S, Nov 3, 2020 · source ↗
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- Coloplast NV/SA1 studySame company
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Focus areas
Conditions Coloplast A/S leads ten or more studies in, by study count. A broader condition is left out when almost all its studies are already in a narrower one listed here.
Studies
Recruiting first, then most recently updated. Showing 50 of 181. Browse all 181 →
- Post-operative Use of New Adhesive After Total LaryngectomyRecruitingNCT07366281Not applicable
Sponsor listed in the registry: Atos Medical AB · First submitted after Atos Medical AB became part of Coloplast A/S
- Urine Research BiobankRecruitingNCT07769606
- Use of TrachPhone in Tracheostomized PatientsEnrolling by invitationNCT06487104Not applicable
Sponsor listed in the registry: Atos Medical AB · First submitted after Atos Medical AB became part of Coloplast A/S
- CP384 - Ostomy Care (OC) PRO Panel PlanNot yet recruitingNCT07589907
- CP382 - Intermittent Catheter (IC) PRO Panel PlanNot yet recruitingNCT07475468
- Exploratory Study Investigating the Urinary Bladder During Intermittent Catheterization in Healthy and Spinal Cord Injured Male and Female Subjects Using an Upright MRI ScannerNot yet recruitingNCT07384559Not applicable
- Evaluating Whether Intact Fish Skin Graft Can Decrease the Need for Autograft in the Treatment of Deep Partial-Thickness BurnsEnrolling by invitationNCT07326657Phase 4
Sponsor listed in the registry: Kerecis Ltd. · First submitted after Kerecis Ltd. became part of Coloplast A/S
- Prospective Longitudinal Study of Heylo™ for People Living With a StomaRecruitingNCT06554015
- Feasibility of a Newly Developed Ostomy PrototypeNot yet recruitingNCT07146035Not applicable
- Evaluating the Durability of Closure for Venous Leg UlcersRecruitingNCT06697925
Sponsor listed in the registry: Kerecis Ltd. · First submitted after Kerecis Ltd. became part of Coloplast A/S
- Evaluating Intact Fish Skin Graft and Standard of Care Versus Standard of Care Alone in Nonhealing Venous Leg UlcersRecruitingNCT06693570Phase 4
Sponsor listed in the registry: Kerecis Ltd. · First submitted after Kerecis Ltd. became part of Coloplast A/S
- Kerecis Real-World Fish Skin Graft RegistryEnrolling by invitationNCT06384183
Sponsor listed in the registry: Kerecis Ltd. · First submitted after Kerecis Ltd. became part of Coloplast A/S
- TFL Driven Urinary System Treatment StudyRecruitingNCT06257368
- A 3 Years Naturalistic Cohort Survey Of Virtue® Male Sling System For Male Stress Urinary IncontinenceRecruitingNCT04098822
- INTIBIA Pivotal StudyActive, not recruitingNCT05250908Not applicable
- Peristeen Light Explorative Clinical InvestigationCompletedNCT07126327Not applicable
- New Coating for Urinary Intermittent CathetersCompletedNCT06985888Not applicable
- Define Final Selection Choice Criteria for a Coloplast Catheter Ensuring Highest Patient Satisfaction Via Surveys (EVA).TerminatedNCT07355803Not applicable
Sponsor listed in the registry: Coloplast NV/SA
- Biatain Silicone Sacral for Pressure Injury Prevention in Hospital-admitted Patients at RiskCompletedNCT05619003Not applicable
- A 3 Years Naturalistic Cohort Survey of Altis Single Incision Sling System For Female Stress Urinary IncontinenceTerminatedNCT04115605
- Clinical Investigation Exploring a Newly Developed Ostomy BaseplateCompletedNCT07376421Not applicable
- Real-Life Use of Transabdominal Restorelle® Meshes in Apical Prolapse RepairTerminatedNCT06296316
- Clinical Investigation Exploring a Newly Developed Ostomy Baseplate.CompletedNCT07316530Not applicable
- Intermittent Catheterisation on the Bladder Mucosa of Healthy Volunteers With a Prototype Micro Hole Zone CatheterCompletedNCT05224544Not applicable
- Long Term Effects of Heat and Moisture Exchangers (HMEs)CompletedNCT06084611Not applicable
Sponsor listed in the registry: Atos Medical AB · First submitted after Atos Medical AB became part of Coloplast A/S
- Investigation of the Clinical Performance of Biatain Fiber Ag on BurnsCompletedNCT05824026Not applicable
- A Pilot Evaluation Exploring New Adhesive Materials and Their Ability to Adhere to Abdominal and Peristomal SkinCompletedNCT05641168Not applicable
- Evaluation of the Influence of Output on Skin Covered by Adhesives (Round 5)CompletedNCT02992444Not applicable
- A Pilot Evaluation of Adhesives and How They Are Impacted by Output (Round 1b)CompletedNCT02626260Not applicable
- Evaluation of the Ability of Newly Developed Adhesives to Absorb MoistureCompletedNCT03619226Not applicable
- Clinical Investigation Exploring Two Ostomy Product PrototypesCompletedNCT06237686Not applicable
- Investigation of a New Rectal Catheter for Users of Transanal IrrigationCompletedNCT06389396Not applicable
- Investigation of the Clinical Performance of Biatain Fiber Ag on Venous Leg UlcersCompletedNCT05873257Not applicable
- A RCT Evaluating the Clinical Benefit of a Silver Dressing in the Treatment of Venous Leg UlcersCompletedNCT05923749Not applicable
- CP376 OCT Exploratory Skin StudyCompletedNCT06965140Not applicable
- A Randomized Controlled Clinical Investigation Evaluating a Flat Ostomy Barrier With A Novel Skin Protection TechnologyCompletedNCT04868617Not applicable
- Evaluation of the Peel Force of New Adhesives From the SkinCompletedNCT03200444Not applicable
- Assessment of New Enhanced Ostomy Device in Real-life Settings in Subjects Having a StomaCompletedNCT03770078Not applicable
- A Clinical Investigation Evaluating Three New 1-piece Ostomy ProductsCompletedNCT03154944Not applicable
- Explorative Clinical Study on the Performance and Acceptance of New Intermittent Catheters in Healthy VolunteersCompletedNCT04231149Not applicable
- A Confirmatory Study Confirming Performance of a New Intermittent CatheterCompletedNCT05485935Not applicable
- Performance and Safety Evaluation of the SenSura® Mio Baby Device in Subjects With a StomaWithdrawnNCT03929978
- Performance of a Single-use Intermittent Micro-hole Zone CatheterCompletedNCT05485922Not applicable
- Clinical Performance and Cost Effectiveness of Biatain® Silicone Compared With Standard of CareCompletedNCT05786612Not applicable
- Clinical Trial of New Intermittent Single-use CatheterCompletedNCT05814211Not applicable
- Clinical Investigation of an Improved Two-piece Stoma Product for People Living With a StomaCompletedNCT05652010Not applicable
- Clinical Trial of New Single-use Compact Intermittent CatheterCompletedNCT05841004Not applicable
- Investigation of Heylo, a Novel App Driven Digital Supporting Ostomy ProductCompletedNCT05200416Not applicable
- Kerecis Case Registry for SurgiBind : Soft Tissue ReinforcementActive, not recruitingNCT05898711
Sponsor listed in the registry: Kerecis Ltd. · First submitted before Kerecis Ltd. became part of Coloplast A/S
- AFS Compared to AHC in Treatment of Necrotizing Fasciitis NFActive, not recruitingNCT06073301Phase 4
Sponsor listed in the registry: Kerecis Ltd. · First submitted after Kerecis Ltd. became part of Coloplast A/S